AU2013209081B2

AU2013209081B2 - Kit for producing a vaccine

Info

Publication number: AU2013209081B2
Application number: AU2013209081A
Authority: AU
Inventors: Gerald BEHRENS; Knut Elbers; Dirk Neven RAULEDER
Original assignee: Boehringer Ingelheim Vetmedica GmbH
Current assignee: Boehringer Ingelheim Vetmedica GmbH
Priority date: 2012-01-13
Filing date: 2013-01-14
Publication date: 2017-10-05
Anticipated expiration: 2033-01-14
Also published as: KR20140112508A; EP2802348B1; BR112014017031A2; BR112014017031B1; EA201400812A1; CL2014001798A1; AU2013209081A1; CA2860631A1; JP2015508312A; CN104039347A; BR112014017031A8; SG11201403957WA; CA2860631C; WO2013104550A1; EP2802348A1; DE202013007396U1; PL2802348T3; EA033354B1

Abstract

The invention relates to a kit, to a use, and to a method for producing a vaccine for immunizing against porcine circovirus disease and/or enzootic pneumonia of pigs, wherein a first container is filled only partially with a first vaccine and a second container is filled with a second component, wherein the second vaccine is transferred into the first container by means of an adapter device by penetrating a closing device for the first time and/or one time only and the vaccine is produced in the first container, which enables a simple, less error-prone and more hygienic operation with reduced material use.

Description

- 1-

Kit for the preparation of a vaccinating agent

The present invention relates to a kit for the preparation of a vaccinating agent, a use of the kit for preparing a vaccinating agent, a use of at least two starting materials for preparing a vaccinating agent and a process for providing a vaccinating agent

The present invention relates in particular to the manufacture and provision of vaccinating agents, particularly in the veterinary medical field. Primarily, the present invention relates to vaccinating agents for immunising pigs against Porcine Circovirus, particularly type 2, also known as Porcine Circovirus Disease or PCVD, and/or against bacteria of the strain Mycoplasma hyopneumoniae, also known as Enzootic Pneumonia or EP.

It is known that the above-mentioned diseases can be prevented by immunisation with vaccines. Vaccinating agents are usually provided for injection and have to be correspondingly sterile. Moreover, each individual injection causes stress to the creature being treated and for this reason the number of vaccination processes should be kept to a minimum.

One known possibility for reducing the number of vaccination processes are so-called combined vaccinations by which immunisation against different diseases can be provided in just a few or even just one session. However, a combined vaccination is often not possible as a result of incompatibilities of different vaccines or components thereof with one another. Even if an at least short-time compatibility can be achieved, these combination vaccines have to be produced on site. In the veterinary medical field, in particular, the vaccines then have to be prepared and/or administered outdoors. A problem here is that the combination vaccine may become contaminated, for example with pathogens, particularly if a mixing vessel has to be punctured several times.

Object of the present invention is to provide a kit for preparing a vaccinating agent, a use of this kit for preparing a vaccinating agent, a use of two starting materials for preparing a vaccinating agent and a process for providing a vaccinating agent by which a vaccinating agent can be produced, even from starting materials which are only briefly stable with one another, by the simplest possible method, which is not prone to errors and is at the same time hygienic.

The above problem is solved by a kit for preparing a vaccinating agent according to claim 1, by a use of such a kit for preparing a vaccinating agent according to claim 55, by a use of at least two starting materials for preparing a vaccinating agent according to claim 56 or - 2 - by a process for providing a vaccinating agent according to claim 116. Advantageous embodiments are the subject of the sub-claims.

In a first aspect the present invention relates to a kit for preparing a vaccinating agent, particularly for preparing a vaccinating agent for use in immunising against the disease Porcine Circovirus Disease "PCVD" and/or Enzootic Pneumonia "EP" or against infections with Porcine Circovirus, particularly type 2, and/or Mycoplasma hyopneumoniae.

The kit according to the invention comprises a first starting material and a second starting material that is different from the first A starting material for the purposes of the present invention is preferably any source material, particularly a vaccine, a source material comprising a vaccine and/or a component or source material for a vaccinating agent, preferably an antigen or a composition containing an antigen.

Moreover, the kit comprises a first container that is only partly filled with the first starting material and a second container holding the second starting material. A container for the purposes of the present invention is preferably a structure enclosing a volume, preferably configured to receive a liquid, particularly a vessel, a bottle, a bag or the like.

The kit further comprises an adapter device for establishing a fluid connection, wherein the fluid connection can be established between the first and second containers. It is also preferable that the adapter device should be configured to establish a fluid connection between the interiors of the first container and the second container.

Moreover in the proposed kit at least one of the containers is closed off by a closure device on the operating side. Preferably, both containers are closed off by a closure device on the operating side. Preferably, an airtight and/or sterile closure is provided. In particular this may be a seal, a rubber stopper or the like, wherein the closure device can preferably be penetrated and/or pierced, particularly reversibly. In this way the containers, i.e. at least one of the containers, can be sealed in sterile manner.

It is envisaged that the second container can be connected to the first container by means of the adapter device, when the closure device is pierced for the first and/or only time, - 3 - such that the second starting material enters the first container, particularly is transported therein, and there forms the vaccinating agent with the first starting material. The closure device or closure devices are thus preferably embodied to be penetrated or pierced by means of the adapter device. The adapter device is preferably configured to be able to penetrate and/or pierce the closure device or closure devices. In this way a fluid connection can be provided between the first and second containers.

With the kit according to the invention it is thus possible to prepare a vaccinating agent from two starting materials with only two containers and an adapter device, particularly for use in immunising against the diseases caused by infections with Porcine Circovirus and/or Mycoplasma hyopneumoniae, preferably for use in immunising against the diseases caused by infections with Porcine Circovirus and Mycoplasma hyopneumoniae. The kit also avoids the use of other incompatible starting materials, particularly by presenting the starting materials and containers in kit form.

Advantageously, the vaccinating agent may be formed in the only partly filled first container, avoiding the need for additional containers and/or additional adapter devices. This makes the application as simple as possible. In addition, the use of materials is minimised as the number of components required is reduced to a minimum.

Also it is particularly advantageous that simply penetrating or piercing the closure device, for the first or only time, is enough to produce the vaccinating agent. In fact, this avoids foreign substances or pathogens getting into the vaccinating agent during multiple penetration or piercing of the closure device.

In the present invention, for reasons of clarity, a distinction is made between vaccines as possible constituents of one or more starting materials and the vaccinating agent as the product prepared from the starting materials.

Thus, the term "vaccinating agent", even when it also denotes a vaccine, preferably denotes the end product that is preferably produced or prepared from the two starting materials and/or is used for the treatment Particularly preferably, the vaccinating agent is a combination vaccine, preferably containing at least two vaccines different from one another or at least two antigens different from one another or two compositions containing antigen, where the compositions containing the antigen differ at least in the antigens present The term "vaccines", even when it refers to vaccinating agents, preferably refers to starting materials or constituents thereof, particularly antigens or antigen-containing compositions. By an "antigen" or an "antigen-containing composition" is preferably meant - 4-a substance or a composition containing the substance which can elicit an immune response in an animal after administration or can intensify an existing immune response. The differentiation between the terms "vaccinating agent" and "vaccine" thus serves mainly only to clarify or to distinguish the product from possible components of one or more of the starting materials. Consequently it is possible to replace the term "vaccinating agent" by the term "vaccine" or vice versa. A kit, under the terms of the present invention, is in particular a combination and/or system comprising the first container, the second container and preferably the adapter device, which form components of the kit The components of the kit are preferably sold as a set, particularly in a combined package or the like. However, it is also possible for the components specified to form a loose combination for joint use. A common or linking component may be provided, for example a common instruction manual, recommendations for use, references in the captions on one or more of the components of the kit or the like.

Another aspect of the present invention that can also be implemented independently relates to the use of a preferably proposed kit for the preparation and/or provision of a vaccinating agent, particularly for immunising against the disease(s] Porcine Circovirus Disease "PCVD" and/or Enzootic Pneumonia "EP" or infections with Porcine Circovirus and/or infection with bacteria of the Mycoplasma strain, particularly Mycoplasma hy-opneumoniae, preferably for immunisation against the diseases Porcine Circovirus Disease "PCVD" and/or Enzootic Pneumonia "EP" or against infections with Porcine Circovirus, particularly Porcine Circovirus type 2 and infection with bacteria of the Mycoplasma strain, particularly Mycoplasma hyopneumoniae.

Another aspect of the present invention that can also be implemented independently relates to the use of at least two starting materials for preparing a vaccinating agent, particularly for simultaneous immunisation, in particular, against the disease(s) Porcine Circovirus Disease "PCVD" and/or Enzootic Pneumonia "EP", preferably for in particular simultaneous immunisation against the diseases Porcine Circovirus Disease "PCVD" and Enzootic Pneumonia "EP", or against infections with Porcine Circovirus, particularly Porcine Circovirus Type 2 and infection with bacteria of the Mycoplasma strain, particularly Mycoplasma hyopneumoniae, wherein the vaccinating agent is prepared using starting materials in containers and an adapter device. A kit may be used as proposed.

It is also envisaged that a first starting material is used in a first container only partly filled with the first starting material and a second starting material that is different from the first is used in a second container holding the second starting material and an adapter de--5-vice is used which is configured so as to establish a fluid connection between the first and second containers. At least one of the containers is closed off by a closure device on its operating side. A fluid connection between the first and second containers is produced by means of the adapter device when the closure device is penetrated for the first and/or only time, in order to transfer the second starting material through the adapter device and closure device into the first container and produce the vaccinating agent in the first container.

Another aspect of the present invention that can also be implemented independently relates to a process for preparing a vaccinating agent from a first starting material and a second starting material different from the first, particularly for especially simultaneous immunisation against the disease Porcine Circovirus Disease "PCVD" and/or Enzootic Pneumonia "EP", preferably for particularly simultaneous immunisation against the diseases Porcine Circovirus Disease "PCVD" and Enzootic Pneumonia "EP". The vaccinating agent may be prepared using a kit as proposed.

Between a first container only partly filled with the first starting material and a second container holding the second starting material a fluid connection is established by an adapter device, such that the fluid connection between the first and second containers is established by means of the adapter device when at least one closure device, which preferably closes off at least one of the containers and is provided on the operating side, is penetrated or pierced for the first and/or only time by the adapter device. The second starting material is transferred or conveyed through the adapter device and the closure device into the first container. In the first container, the vaccinating agent is formed from the first starting material and the second starting material.

Preferably, the first and/or second starting material is or comprises a vaccine, an antigen and/or an antigen-containing composition. Moreover, the first starting material may differ from the second starting material. The first starting material may thus be or comprise a first vaccine, a first antigen and/or a composition containing a first antigen and the second starting material may be or comprise a second vaccine, different from the first, a second antigen different from the first and/or an antigen-containing composition, the antigen of which differs from that of the first antigen-containing composition. Preferably, the first vaccine and the second vaccine, or the first antigen and the second antigen, or the compositions containing the various antigens are for particularly simultaneous immunisation against various diseases or pathogens such as for example against the disease Porcine Circovirus Disease "PCVD" and Enzootic Pneumonia "EP", or for immunisation against Porcine Circovirus, preferably Porcine Circovirus type 2 and against Mycoplasmas, preferably against Mycoplasma hyopneumoniae. This makes it possible to produce a combination vaccine. The starting materials may contain other substances apart from vaccines, particularly water, adjuvants and/or excipients. -6-

It is particularly preferable that the first starting material comprises only a first of the components Mycoplasma vaccine or Mycoplasma antigen, respectively, and Circovirus vaccine or Circovirus antigen, respectively, (and optionally other substances]. The first starting material may thus comprise either Mycoplasma vaccine, or one or more Mycoplasma antigens or alternatively Circovirus vaccine or one or more Circovirus antigens.

The first starting material is preferably stored separately from the second starting material, particularly if the starting materials are not stable together in the long term. The second starting material preferably only comprises the other of the components Mycoplasma vaccine or one or more Mycoplasma antigens and Circovirus vaccine or one or more Circovirus antigens (and optionally other substances]. Thus, if the first starting material contains Mycoplasma vaccine or one or more Mycoplasma antigens, the second starting material contains Circovirus vaccine or one or more Circovirus antigens or vice versa.

The Mycoplasma vaccine may comprise attenuated and/or inactivated bacteria, fragments of bacteria or recombinantly produced parts of Mycoplasma hyopneumoniae, but at least one or more Mycoplasma hyopneumoniae antigens. Preferably, the Mycoplasma hyopneumoniae antigen originates from the Mycoplasma hyopneumoniae strain J or the inactivated Mycoplasma hyopneumoniae bacteria are those of the strain J. Moreover, the Mycoplasma vaccine may be one of the following vaccines or the Mycoplasma hyopneumoniae antigen may be the antigen or antigens contained in one of the following vaccines: IngelvacOMycoFlex (Boehringer Ingelheim Vetmedica Inc, St Joseph, MO, USA), Porcilis M. hyo, Myco Silencer® BPM, Myco Silencer® BPME, Myco Silencer® ME, Myco Silencer® M, Myco Silencer® Once, Myco Silencer® MEH (all from Intervetlnc., Millsboro, USA), Stel-lamune Mycoplasma (Pfizer Inc., New York, NY, USA), Suvaxyn Mycoplasma, Suvaxyn M. hyo, Suvaxyn MH-One (all previously from Fort Dodge Animal Health, Overland Park, KS, USA (now Pfizer Animal Health).

The Circovirus vaccine may comprise attenuated and/or inactivated porcine Circovirus, preferably type 2, particularly type 2 ORF2 protein. It is particularly preferable to use recombinantly expressed ORF2 protein of Porcine Circovirus type 2, preferably expressed in and obtained from in vitro cell culture. Examples of ORF2 proteins of Porcine Circovirus type 2 are described inter alia in International Patent Application W02006-072065. These have proved particularly advantageous for effective vaccination. Moreover, the Circovirus vaccine may be one of the following vaccines, or the Circovirus antigen may be the antigen or antigens contained in one of the following vaccines: Ingelvac®CircoFLEX, (Boehringer Ingelheim Vetmedica Inc, St Joseph, MO, USA), CircoVac® (Merial SAS, Lyon, France), CircoVent (Intervet Inc., Millsboro, DE, USA), or Suvaxyn PCV-2 One Dose® (Fort Dodge Animal Health, Kansas City, KA, USA). -7-

The Circovirus vaccine, if it contains the ORF2 protein, preferably contains between 2 μg and 150 pg, preferably between 2 μg and 60 pg, more preferably between 2 μg and 50 pg, more preferably between 2μg and 40 μg, more preferably between 2 pg and 30 pg, more preferably between 2pg and 25 pg, more preferably between 2pg and 20 pg, more preferably between 4 pg and 20 pg, more preferably between 4pg and 16 pg ORF2 protein per dose to be administered. The Circovirus vaccine is preferably produced or designed so that 1 ml of the vaccine corresponds to a dose of 1 and/or one (single] dose. In particular the Circovirus vaccine may contain ORF2 protein in amounts of more than 2 pg/ml, preferably more than 4 pg/ml and/or less than 150 pg/ml, preferably less than 60 pg/ml, 50 pg/ml, 40 pg/ml, 30 pg/ml or 25 pg/ml, particularly less than 20 pg/ml. This helps to ensure reliable administration.

The Mycoplasma vaccine, if it contains inactivated Mycoplasma bacteria, preferably inactivated Mycoplasma hyopneumoniae bacteria, preferably contains between 103 and 109 colony forming units (CFU], preferably between 104 and 108 (CFU], more preferably between 105 and 106 (CFU] per dose to be administered, the corresponding CFU being selected before the inactivation of the bacteria. The Mycoplasma vaccine is preferably prepared or designed such that 1 ml of the vaccine corresponds to a dose of 1 and/or one (single] dose. In particular, the mycoplasma vaccine may contain more than 103 CFU/ml, preferably more than 104 CFU/ml, particularly more than 105 CFU/ml and/or less than 109 CFU/ml, preferably less than 108 CFU/ml, particularly less than 107 CFU/ml or 106 CFU/ml inactivated Mycoplasma bacteria, preferably inactivated Mycoplasma hyoneumoniae bacteria, particularly before the inactivation of the bacteria.

At least one of the starting materials and/or the vaccinating agent may contain an adjuvant, preferably a polymeric adjuvant, particularly carbomer. Preferably, at least or exactly one of the two starting materials, preferably both starting materials, contain a quantity of adjuvant of 500 pg to 5 mg, preferably 750 pg to 2.5 mg, more preferably about 1 mg of adjuvant per dose to be administered. The starting materials are preferably prepared or designed such that 1 ml of the respective starting material corresponds to a dose of 1 and/or one (single] dose. The use of an adjuvant, preferably a polymeric adjuvant, such as carbomer, for example, has proved advantageous in terms of the efficiency of the immunisation or its duration of effect The use of alternative and/or additional adjuvants is not excluded, however.

It has also proved advantageous if the total volume of the first container exceeds the volume of the first starting material at least by the volume of the second starting material, particularly by more than 2%, preferably more than 5%, particularly more than 8%. This ensures that the first container has sufficient capacity for the second starting material. In addition, the volume of the first container, which exceeds the sum of the volumes of the first and second starting material, ensures effective mixing of the starting material, partic-8 2013209081 13 Sep 2017 ularly when the first container is moved after the transfer of the second starting material into the first container.

It is thus preferable on the one hand that the total volume of the first container should exceed the sum of the volumes of the starting materials. On the other hand, the first container is moved during and/or after the transfer of the second starting material into the first container, to achieve or speed up homogeneous mixing and/or reaction.

According to another aspect of the present invention, the first container may be used for installation in or use with an injection device. In particular, this is an injection device for multiple use, such as for example an injection gun, a pressure injection and/or a self-filling syringe as used for example for vaccinating larger herds of animals. In this way, the number of penetrations of the closure device of the first container can be minimised. In particular, the number of penetrations can be reduced to two, namely one penetration for the preparation process and a second penetration for drawing up the vaccinating agent. Particularly advantageously, the adapter device may be used for connection to the injection device, thus reducing the number of penetrations to one.

The kit according to the invention may comprise an injection device or be associated with one such. In particular, an opening, a flange or other connecting or closure element of the first container and/or the adapter device may be configured so as to allow direct use in or with an injection device. Moreover, the opening, the flange or the other connecting and/or closure element may be specifically designed for connection to a particular injection device. Once again this decreases the likelihood of incorrect use, particularly of incorrect amounts of active substance or methods of administration.

One or more of the containers may contain, in addition to the respective starting material, a gas, particularly a protective gas, thus making it possible to improve the long-term stability of the respective starting material. Moreover, the adapter device may be embodied to transfer the gas from the first container into the second container when the second starting material is transferred from the second container into the first container, particularly with the exclusion of the surrounding atmosphere. Thus ensures that effects on one or more of the starting materials and/or the vaccinating agent as a result of oxidation or the like, in particular, is ruled out and/or a pressure equalisation is made possible.

AH26(135462001):MBS 8a 2013209081 13 Sep 2017

According to a first aspect of the present invention, there is provided a process for preparing a vaccinating agent from a first starting material in a first container and a second starting material in a second container, wherein the second starting material is different from the first starting material, and wherein said vaccinating agent is used for the simultaneous immunisation of a subject against the diseases Porcine Circovirus Disease "PCVD" and Enzootic Pneumonia "EP", wherein the first starting material and the second starting material are liquid, the first starting material comprises a first of the components of a Mycoplasma vaccine and a Circovirus vaccine, the second starting material comprises the other components of the Mycoplasma vaccine and Circovirus vaccine, and the total volume of the first container exceeds the volume of the first starting material at least by the volume of the second material, wherein between a first container only partly filled with the first starting material and a second container comprising the second starting material a fluid connection is formed by an adapter device, such that, by means of the adapter device, when at least one factory provided closure device of at least one of the containers is pierced for the first and/or only time a fluid connection is formed between the first and second container, and the second starting material is conveyed through the adapter device and the closure device into the first container, and in the first container the vaccinating agent is formed from the first and second starting material.

According to a second aspect of the invention, there is provided a kit for preparing a vaccinating agent according to the process of the first aspect of the present invention when used to immunise against the diseases Porcine Circovirus Disease "PCVD" and Enzootic Pneumonia "EP", the kit comprising: a first starting material and a second starting material, wherein the second starting material is different from the first starting material; a first container only partly filled with the first starting material; and a second container comprising the second starting material, wherein the first starting material and the second starting material are liquid, the first starting material comprises a first of the components Mycoplasma vaccine and Circovirus vaccine, the second starting material comprises the other components of the Mycoplasma vaccine and Circovirus vaccine, and the total volume of the first container exceeds the volume of the first starting material at least by the volume of the second material wherein at least one of the containers is closed off with a factory provided closure device and the second container is connectable to the first container by means of an adapter device by

AH26(13546200_1):MBS 8b 2013209081 13 Sep 2017 piercing the closure device for the first and/or only time, such that the second starting material enters the first container and there forms the vaccinating agent with the first starting material. In a third aspect of the present invention, there is provided use of a kit according to any one of claims 6 to 19, for producing and/or preparing a vaccinating agent, for simultaneous immunisation against the diseases Porcine Circovirus Disease "PCVD" and Enzootic Pneumonia "EP".

Further aspects, details, features, properties and advantages of the present invention will become apparent from the claims and the graphic representation as well as the following

AH26( 13546200 1):MBS -9- description of a preferred embodiment of the proposed kit for preparing a vaccinating agent In the drawings:

Fig. 1 shows a first container, partly filled with a first starting material;

Fig. 2 a second container with a second starting material;

Fig. 3 an adapter device for fluidically connecting the containers;

Fig. 4 a second container with adapter device inserted;

Fig. 5 a first and a second container connected by an adapter device;

Fig. 6 a first container with vaccinating agent;

Fig. 7 an injection device with first container attached.

In the Figures, the same reference numerals are used for identical or similar parts, where corresponding or comparable properties and advantages are obtained even if the description is not repeated.

Fig. 1 shows a first container 1 with a wall 2 delimiting a volume. The container 1 comprises an opening region 3 which may have a flange 4, for example an annular shoulder. Preferably, the container 1 is closed off by a closure device 5, particularly in sterile and/or airtight manner. For this purpose it may be envisaged that the closure device 5 abuts firmly on the flange 4, more particularly is pressed against it

For example, a clamping element 6, particularly a clamping ring, may be provided which presses the closure device 5 against the flange 4. The clamping element 6 may be metallic and may contain aluminium or stainless steel, in particular. Alternatively or additionally, it is possible for the clamping element 6 to include plastics or be made of plastics. The - 10- clamping element 6 is preferably embodied so as to pressure the closure device 5 against the flange 4 and thereby enable the first container 1 to be sealed off, particularly from the environment and/or atmosphere.

In the embodiment shown, the closure device 5 closes off or seals the first container 1. The closure device 5 is preferably penetrable or pierceable for example with a spike, a needle, a hollow needle, a double spike or the like. Particularly preferably, the closure device 5 is configured to be penetrable or pierceable in such a way as to achieve a reversible closure, i.e. even after penetration or piercing and removal of the corresponding agent, the closure device 5 particularly makes it possible to obtain an in particular airtight and/or sterile seal. The closure device 5 may contain rubber, particularly halobutyl type 1 rubber and/or may be in the form of a rubber stopper. However, the closure device 5 may also consist of or contain other materials, particularly materials that are also used for the wall 2.

The wall 2 of the first container 1 preferably comprises a sterilisable material, preferably glass, polyethylene, high density polyethylene (HDPE), ethylenevinylacetate (EVA), halo-butyl type 1 rubber and/or siliconised chlorobutyl. The wall 2 may be of rigid or flexible construction. The first container 1 may be embodied in particular as a bottle, bag, can or the like. In particular, the first container 1 may be a cartridge, an insert or an installation or attachment device for an injection device 22 (cf. Figure 7), as will be discussed in more detail hereinafter.

In the embodiment shown in Figure 1 the container 1 is only partly filled with a first starting material 7. The container 1 is for example filled with the first starting material to an amount of less than 70 %, preferably less than 50 %, particularly less than 45 % and/or more than 10 %, preferably more than 20 %, particularly more than 30 %.

Besides the first starting material the first container 1 may contain a gas 8, particularly a protective gas, noble gas, inert gas or the like. In this way the shelf life of the first starting material 7 can be improved.

Preferably, the sum of the volumes of the first starting material 7 and the gas 8 gives the total volume of the first container 1, preferably therefore the volume enclosed by the wall 2 of the first container 1, particularly with the closure device 5, or a smaller volume.

Figure 2 shows a second container 9 with a second starting material 10. The second container 9 may comprise a wall 11, an opening region 12, a flange 13, a closure device 14 -11- and/or a clamping element 15, which may preferably have the same or similar properties to the corresponding elements of the first container 1, and for this reason the description will not be repeated at this point. Therefore, only possible differences between the second container 9 and the first container 1 will be mentioned hereinafter.

The second container 11 is preferably configured with an at least partially flexible wall 11, wherein in particular pressure can be exerted on the second starting material 10 by pressing on the wall 11. This can help to promote the expulsion or transfer of the second starting material 10.

Preferably, the volume of the gas 8 corresponds to or exceeds the volume of the second starting material 10. In particular, the volume of the gas 8 in the first container 1 exceeds the volume of the second starting material 10 by more than 2 %, preferably more than 5 %, particularly more than 8 % and/or less than 80 %, preferably less than 50 %, particularly less than 40 % or 30 %. This allows the first container 1 to take up minimal space while at the same time preparing the vaccinating agent 21 (cf. Figure 5) in the first container 1. In particular, a sufficient volume of gas 8 remains in the first container 1, thus allowing homogeneous mixing by movement of the first container 1.

In the embodiment shown in Figure 2 the second container 9 is at least substantially filled with the second starting material 10. Alternatively or additionally, however, it is also possible for the second container 9 to be completely filled with the second starting material 10 or only partly filled with the second starting material 10. If the second container 9 is only partly filled with the second starting material 10, a gas 16, particularly a protective gas, may be provided which preferably fills the volume of the second container 9 enclosed by the wall 11, particularly with the closure device 14, together with the second starting material 10.

It is particularly preferred if the total volume of the first container 1 exceeds the volume of the first starting material 7 at least by the volume of the second starting material 10. The volume of the first container 1 thus preferably exceeds the total of the volumes of the first starting material 7 and second starting material 10.

Figure 3 shows an adapter device 17 for providing a fluidic connection between the first container 1 and the second container 9. The adapter device 17 may comprise at least one, preferably two, but also more than two adapter elements 18, particularly needles, hollow needles, spikes, wedges or the like. -12-

The adapter device 17 preferably comprises a fluid channel 19, particularly for fluidically connecting the interiors of the containers 1 and 9. The adapter device 17 is in the form of a double spike or hollow needle in the embodiment shown.

The adapter device 17 may be configured so that during the transfer of the second starting material 10 into the first container 1 the gas 8 or protective gas passes, or more particularly is transported, from the first container 1 into the second container 9. For this purpose the adapter device 17 may comprise a venting and/or exhaust device 20. The venting and/or exhaust device 20 is preferably in the form of a channel, particularly at least substantially parallel to the fluid channel 19. However, other solutions are also possible.

Preferably, the adapter device 17 comprises a channel as the venting and/or exhaust device 20, the openings of which are arranged so that when the second starting material 10 flows out of the second container 9 under the influence of gravity this allows a backflow of the gas 8 from the first container 1 into the second container 9. In particular the opening of the venting and/or exhaust device 20 facing the first container 1 may be recessed relative to the opening of the fluid channel 19 facing the first container 1 in the direction of the longitudinal extent of the adapter device 17 or may be arranged on the side of the opening of the fluid channel 19 remote from the open end of the adapter device 17. The opening of the venting and/or exhaust device 20 facing the second container 9, by contrast, is preferably arranged closer to the open end of the adapter device 17 in relation to the opening of the fluid channel 19 facing the second container 9.

The adapter device 17 in the embodiment shown in Figure 3 is formed in one piece. However it is also possible, alternatively or additionally, for a hose, a tube, or some other flexible or rigid transition to be provided between the adapter elements 18. Preferably, the fluid channel 19 and/or the venting and/or exhaust device 20 connects] the adapter elements 18 with no interruptions. In particular it is possible for a hose, tube or the like to be provided, particularly moulded on, between the adapter elements 18. This permits flexible handling and/or extension of the adapter device 17.

The adapter device 17, particularly one or more of the adapter elements 18, may be configured specifically for the first container 1 and/or for the second container 9. This can be achieved in particular by mechanically configuring at least one of the adapter elements 18 specifically for one of the containers 1, 9, particularly for one of the containers 1, 9 which is associated with the respective adapter element 18, for example by means of a specific thread 3,12, a specific projection, undercut, a specific lug or other structure. In this way substances other than the first starting material 7 and/or the second starting material 10 -13- can be prevented from getting into the first container 1 and/or the second container 9. It is also preferable that the opening region of at least one or both containers 1, 9 is specifically configured for the adapter device 17, particularly for an adapter element 18.

It is also preferable for a connection to be provided only between the containers 1,9, preferably with exclusion of the surrounding atmosphere. For the purposes of the present invention the atmosphere is preferably already deemed to be excluded even when there is still a slight residual volume of atmospheric origin remaining in the adapter device 17, for example less than 10 ml or 5 ml.

The first starting material 7 and/or the second starting material 10 preferably comprise a vaccine. It is also preferable that the starting materials 7,10 should be different, and in particular should contain different vaccines.

As shown in Figures 4 and 5, the adapter device 17 can be used to provide a fluid connection between the first container 1 and the second container 9, wherein the second starting material 10 can preferably be transported into the first container 1 with the assistance of gravity and/or by the exerting of pressure on the second starting material 10 through the wall 11 of the second container 9, in order to form the vaccinating agent 21 with the first starting material 7. The vaccinating agent 21 is preferably intended for preventing pigs becoming ill with infections of Mycoplasma hyopneumoniae and/or Porcine Circovirus, particularly type 2, preferably to prevent pigs becoming ill with infections of Mycoplasma hyopneumoniae and Porcine Circovirus type 2, i.e. in the embodiment shown it is a combination vaccine.

The first container 1, the second container 9 and, preferably, the adapter device 17 preferably form a kit or set, and thus preferably have at least one linking common feature for the purposes of the present invention. This common feature may be that the first container 1, the second container 9 and/or the adapter device 17 are packaged together. Alternatively or additionally it is possible that the first container 1, the second container 9 and/or the adapter device 17 have the same operating instructions, the same in-pack leaflet, the same manufacturer's recommendations or the like. It is also possible for captions, label markings, symbols or other information on the containers 1, 9 to cross-reference one another or the like.

The kit may optionally also comprise other components. Examples of these are one or more injection devices 22, adapter devices for connecting the first container 1 to an injection device 22, some other device or another container. -14-

The kit is preferably intended for preparing a vaccinating agent 21 for preventing diseases caused by infections with Porcine Circovirus type 2 and/or Mycoplasma hyopneumoniae, preferably for preventing diseases caused by infections with Porcine Circovirus type 2 and/or Mycoplasma hyopneumoniae in pigs. However, different applications are not excluded. In particular, it may alternatively be envisaged to use substances other than the vaccines specified or substances or substance mixtures other than starting materials 7,10, and/or to obtain advantages in respect of ease of handling and the reduced likelihood of an ingress of foreign substances, pathogens or the like. In particular, the alternative starting materials may be one or more antigens of the following pathogens: Actinobacillus pleuropneumonia (Al); Adenovirus (A2); Alphavirus such as for example Eastern Equine Encephalomyelitis Virus (A3); Bordetella bronchiseptica (A4); Brachyspira spp. (A5), preferably B. hyodysenteriae (A6); B. piosicoli (A7), Brucella suis, preferably the biovars 1, 2, and 3 (A8); Classical Swine Fever Virus (A9); Clostridium spp. (A10), preferably Cl. difficile (All), Cl. perfringens of types A, B, and C (A12), Cl. novyi (A13), Cl. septicum (A14), Cl. tetani (A15); Coronavirus (A16), preferably Porcine Respiratory Corona Virus (A17); Eperythrozoonosis suis (A18); Eiysipelothrix rhusiopathiae (A19) Escherichia coli (A20); Haemophilus parasuis, preferably of subtypes 1, 7 and 14 (A21) Hemagglutinating Encephalomyelitis Virus (A22); Japanese Encephalitis Virus (A23); Lawsonia intracellularis (A24); Leptospira spp. (A25), preferably Leptospira australis (A26), Leptospira canicola (A27), Leptospira grippotyphosa (A28), Leptospira icterohaemorrhagicae (A29), Leptospira interrogans (A30), Leptospira pomona (A31), Leptospira hardjo (A32) and Leptospira tarassovi (A33); Mycobacterium spp. (A34) preferably M. avium (A35) and M. intracel-lulare (A36); Pasteurella multocida (A37); Porcine Cytomegalovirus (A38); Porcine Parvovirus (A39); Porcine Reproductive and Respiratory Syndrome (PRRS) Virus (A40); Pseudorabies Virus (A41); Rotavirus (A42); Salmonella spp. (A43), preferably S. thyphimurium (A44) and S. choleraesuis (A45); Staphylococcus spp. (A46) preferably Staph, hicus (A47); Streptococcus spp. (A48), preferably Strep, suis (A49); Swine Herpes Virus (A50); Swine Influenza Virus (A51); Swine PoxVirus (A52); Vesicular Stomatitis Virus (A53); Vesicular exanthema of swine virus (A54); and Mycoplasma hyosynoviae (A55). Preferably the starting materials 7 and 10 are different antigens of the pathogens listed here, so that after the mixing of the different starting materials the vaccinating agent 21 can be used for preventing diseases caused by at least two of the pathogens listed here.

To prepare the vaccinating agent 21 the adapter device 17 with an adapter element 18 may be pushed through the closure device 14 of the second container 9 into the interior thereof, particularly as shown in Figure 4. The closure device 14 is thus preferably penetrated by the adapter device 17, particularly an adapter element 18 thereof.

Moreover, in particular, as shown in Figure 5, the combination of the second container 9 and adapter device 17, particularly with another adapter element 18 of the adapter device -15- 17, may be pushed through the closure device 5 of the first container 1 into the interior thereof. Preferably, the adapter device 17 or the adapter element 18 penetrates the closure device 5 of the first container 1. In this way it is possible for the adapter device 17 to provide a fluid connection 20 between the interiors of the first container 1 and the second container 9.

In Figures 4 and 5, details of the opening regions 3,12 of the containers 1, 9 and the adapter device 17 are not shown, for reasons of clarity. Reference is made to Figures 1 to 3 on this subject

As shown in Figure 5, the second starting material 10 may be transferred through the adapter device 17 into the first container 1, preferably using gravity and/or by compression of the preferably flexibly formed second container 9. Alternative and/or additional methods or procedures for transferring the second starting material 10 into the first container 1 are also possible.

In another example, not shown, first the adapter device 17 is used to penetrate the closure device 5 of the first container 1. In a second step the second container 9 is then fitted onto the adapter device 17 already inserted into the first container 1 or is otherwise connected to the adapter device 17 such that a fluidic connection 20 is formed between the first container 1 and the second container 9. In each case it is preferable, after inserting the adapter device 17 into a first of the containers 1, 9, that the one of the containers 1,9 that is not yet attached to the adapter device 17 is fitted onto the vertically positioned combination of adapter device 17 and the other one of the containers 1, 9. This prevents one of the starting materials 7,10 from flowing out

In one aspect the present invention relates to the penetration, for the first and/or only time, of at least one of the closure devices 5,14 by the adapter device 17. Particularly preferably, both containers 1,9 comprise closure devices 5,14, which are each penetrated, pierced or perforated for the first and/or only time. This is made possible, in the embodiment shown, by the fact that the first container 1 is only partly filled with the first starting material 7. Advantageously this makes it possible to produce the vaccinating agent 21, particularly the combination vaccine, without having to use a plurality of adapter devices 17 or more than two containers 1,9. This results in a simple, reliable and clear operation, in which the vaccinating agent 21 is prepared using only one adapter device 17, thus effectively preventing mix-ups with other starting materials and the introduction of impurities or pathogens. -16-

These positive properties can be further enhanced if the first container 1, optionally with the adapter device 17, is configured to be used directly in the injection device 22, particularly in an injection gun, in a pressure injector and/or in a self-filling syringe (cf. Figure 7) or with these devices. The first container 1 can thus be used in or with a preferably multiple-use injection device 22. This means that each closure device 5,14 only has to be pierced or penetrated on a first and only occasion. This allows a high degree of safety of use, ease of handling and hygiene.

It may be envisaged that the first container 1 is configured for use in or with an injection device 22 in a neck or mouth region, particularly in the opening region 3, for connection to an in particular multiple-use injection device 22. The injection device 22 may have a receptacle 23 for the first container 1. It may be provided that the longitudinal extent and/or the diameter of the first container 1 is configured for use in an injection device 22 that is, in particular, designed for multiple use. For example, the first container 1 may have a diameter of more than 1 cm, preferably more than 2 cm, particularly more than 3 cm and/or less than 10 cm, preferably less than 8 cm, particularly less than 6 cm. Alternatively or additionally it is possible for the first container 1 to have a longitudinal extent which is more than 3 cm, preferably more than 5 cm, particularly more than 6 cm and/or less than 30 cm, preferably less than 25 cm, particularly less than 20 cm.

As soon as the second starting material 10 has passed through the adapter device 17 into the first container 1, vaccinating agent 21 can be formed. It is possible that the vaccinating agent 21 is produced by mixing the starting materials 7,10, by dissolving the starting materials 7,10 in one another and/or by reacting the starting materials 7,10 or parts thereof with one another. Preferably, as shown by the arrow in Figure 6, the first container 1 holding the starting materials 7,10 is set in motion, particularly shaken, titled, set in rotation or the like. This ensures or assists with homogeneous and/or faster mixing, reaction and/or dissolving.

In the embodiment shown the first starting material 7 and/or the second starting material 10 comprises vaccine preferably in amounts of more than 30 per cent by weight, preferably more than 40 per cent by weight, particularly more than 50 per cent by weight; and/or less than 90 per cent by weight, preferably less than 80 per cent by weight, particularly less than 70 per cent by weight. Moreover, the first starting material 7, the second starting material 10, and/or the vaccinating agent 21 formed thereby may be a suspension, preferably with vaccines and/or insoluble proteins, preferably in amounts of more than 30 per cent by weight, preferably more than 40 per cent by weight, particularly more than 5 0 per cent by weight; and/or less than 90 per cent by weight, preferably less than 80 per cent by weight, particularly less than 70 per cent by weight This ensures an efficacy, with small amounts of vaccinating agent and at the same time low enough viscosity, which assists with administration. - 17-

The second starting material 10 preferably comprises only the other one of the components Mycoplasma vaccine or Mycoplasma antigen and Circovirus vaccine or Circovirus antigen. It is also preferable if the first starting material 7 comprises Mycoplasma vaccine or one or more Mycoplasma antigens, the first starting material 7 does not comprise Circovirus vaccine or Circovirus antigen, but for this purpose the second starting material 10 comprises Circovirus vaccine or one or more Circovirus antigens, but not Mycoplasma vaccine or Mycoplasma antigen. However, it is not ruled out, for any of the starting materials 7,10, that the particular starting material should not contain additional substances. These might be water, excipients, adjuvants, preservatives or the like.

In one embodiment the ratio by volume of the first starting material 7 to the second starting material 10 is 3:1 to 1:3, preferably 2:1 to 1:2, particularly about 1:1. The first starting material 7 and/or the second starting material 10 and/or the vaccinating agent 21 may have a viscosity that is less than 10,000 mPa-s, preferably less than 1000 mPa-s, particularly less than 500 mPa-s; and/or more than 5 mPa-s, preferably more than 10 mPa-s, particularly more than 2 0 mPa-s, measured with a Brookfield viscometer according to EN ISO 2555 at 5°C. Preferably, the first starting material 7 and/or the second starting material 10 are liquid at 2°C to 8°C and/or have a melting point which is less than 1°C, preferably less than 0°C, particularly less than -0.2°C and/or higher than -1.5°C, preferably higher than -1°C, particularly higher than -0.8°C.

According to another aspect of the present invention it is preferable that the vaccinating agent 21 has a characteristic colour which is different from the two starting materials 7, 10. The specific colour of the vaccinating agent may be formed for example by mixing the differently coloured starting materials 7 and 10. For example, mixing a yellow starting material 7 with a red starting material 10 results in a vaccinating agent 21 that is orange in colour. It is possible for dye components in the starting materials 7,10 to produce the characteristic colour by reaction or other interactions during the preparation of the vaccinating agent 21. Alternatively or additionally the vaccinating agent 21, in contrast to at least one of the starting materials 7,10, may have one colour or no colour. As a result, by means of the characteristic colour, it is possible to ensure that the vaccinating agent 21 has been successfully prepared. This is also possible if at least one of the starting materials has a colour but, once prepared, the vaccinating agent 21 does not.

As already stated above, the Mycoplasma vaccine may comprise attenuated and/or inactivated bacteria, fragments of bacteria or recombinantly prepared parts of Mycoplasma hy-opneumoniae, but at least one or more Mycoplasma hyopneumoniae antigens. Preferably, the Mycoplasma hyopneumoniae antigen originates from the Mycoplasma hyopneumoniae strain J, or the inactivated Mycoplasma hyopneumoniae bacteria are those of the strain J. - 18-

Moreover, the Mycoplasma vaccine may be one of the following vaccines or the Mycoplasma hyopneumoniae antigen may be the antigens contained in one of the following vaccines: Ingelvac®MycoFlex (Boehringer Ingelheim Vetmedica Inc, St Joseph, MO, USA], Porcilis M. hyo, Myco Silencer® BPM, Myco Silencer® BPME, Myco Silencer® ME, Myco Silencer® M, Myco Silencer® Once, Myco Silencer® MEH (all obtainable from Intervet Inc., Millsboro, USA] Stellamune Mycoplasma (Pfizer Inc., New York, NY, USA], Suvaxyn Mycoplasma, Suvaxyn M. hyo, Suvaxyn MH-One (all formerly from Fort Dodge Animal Health, Overland Park, KS, USA (now Pfizer Animal Health],

The Circovirus vaccine may comprise attenuated and/or inactivated porcine Circovirus, preferably type 2, particularly type 2 ORF2 protein. It is particularly preferable to use re-combinantly expressed 0RF2 protein of Porcine Circovirus type 2, preferably expressed in and/or obtained from in vitro cell culture. Examples of 0RF2 proteins of Porcine Circovirus type 2 are described inter alia in International Patent Application W02006-072065. These have proved particularly advantageous for effective vaccination. Moreover, the Circovirus vaccine may be one of the following vaccines, or the Circovirus antigen may be the antigen or antigens present in one of the following vaccines: Ingelvac®CircoFLEX, (Boehringer Ingelheim Vetmedica Inc, St Joseph, MO, USA], CircoVac® (Merial SAS, Lyon, France], CircoVent (Intervet Inc., Millsboro, DE, USA], or Suvaxyn PCV-2 One Dose® (Fort Dodge Animal Health, Kansas City, KA, USA],

The Circovirus vaccine, if it contains the ORF2 protein, preferably contains between 2 pg and 150 pg, preferably between 2 pg and 60 pg, more preferably between 2 pg and 50 pg, more preferably between 2pg and 40 pg, more preferably between 2 pg and 30 pg, more preferably between 2pg and 25 pg, more preferably between 2pg and 20 pg, more preferably between 4 pg and 20 pg, more preferably between 4pg and 16 pg of ORF2 protein per dose to be administered. The Circovirus vaccine is preferably prepared or designed so that 1 ml of the vaccine corresponds to a dose of 1 and/or one (single) dose.

The Mycoplasma vaccine, if it contains inactivated Mycoplasma bacteria, preferably inactivated Mycoplasma hyopneumoniae bacteria, preferably contains between 103 and 109 colony forming units (CFU), preferably between 104 and 108 (CFU), more preferably between 105 and 106 (CFU) per dose to be administered, the corresponding CFU being adjusted before the inactivation of the bacteria. The Mycoplasma vaccine is preferably prepared or designed so that 1 ml of the vaccine corresponds to a dose of 1 and/or one (single) dose.

The Mycoplasma vaccine may preferably comprise attenuated and/or inactivated bacteria or fragments of bacteria of the strain Mycoplasma hyopneumoniae or corresponding antigens, preferably in amounts of more than 30 per cent by weight, preferably more than 40 - 19- per cent by weight, particularly more than 50 per cent by weight; and/or less than 90 per cent by weight, preferably less than 80 per cent by weight, particularly less than 70 per cent by weight.

The Circovirus vaccine may preferably comprise attenuated and/or inactivated Porcine Circovirus, preferably type 2, particularly Porcine Circovirus type 2 ORF2 protein or corresponding antigens, preferably in amounts of more than 30 per cent by weight, preferably more than 40 per cent by weight, particularly more than 50 per cent by weight; and/or less than 90 per cent by weight, preferably less than 80 per cent by weight, particularly less than 70 per cent by weight.

Moreover, at least one of the starting materials 7,10 and/or the vaccinating agent 21 may comprise one, preferably polymeric, adjuvant, particularly carbomer. Preferably one of the two starting materials or, more preferably both starting materials, contain an amount of adjuvant of from 500 pg to 5 mg, preferably from 750 pg to 2.5 mg, more preferably about 1 mg per dose to be administered. The starting materials are preferably prepared or designed so that 1 ml of the respective starting material corresponds to a dose of 1 and/or one (single) dose. In particular, at least one of the starting materials 7,10 may thus comprise one or more adjuvants in a total amount of more than 500 pg/ml, preferably more than 750 pg/ml and/or less than 5 mg/ml, preferably less than 2.5 mg/ml.

It is also possible for at least one of the starting materials 7,10 and/or the vaccinating agent 21 to contain an adjuvant in amounts of more than 0.1 per cent by weight, preferably more than 1 per cent by weight, particularly more than 2 per cent by weight; and/or less than 20 per cent by weight, preferably less than 10 per cent by weight, particularly less than 5 per cent by weight It is also possible for a preferably polymeric adjuvant, particularly carbomer, to be formed in the vaccinating agent 21.

The Mycoplasma vaccine and/or the Circovirus vaccine or at least one of the starting materials 7,10, and/or the vaccinating agent 21 may contain formaldehyde, preferably in a concentration of less than 2.5 mg/m3, preferably less than 1.5 mg/m3, particularly 0.74 mg/m3 or less. Alternatively or additionally, at least one of the starting materials 7,10, preferably both starting materials 7,10, may contain water in a concentration of at least 20 per cent by weight, preferably at least 30 per cent by weight, particularly at least 40 per cent by weight; and/or at most 80 per cent by weight, preferably at most 70 per cent by weight, particularly at most 60 per cent by weight. -20-

The first starting material 7, the second starting material 10 and/or the vaccinating agent 21 may comprise one or more excipients, particularly a preservative, an antioxidant and/or an emulsifier, preferably in a concentration of at least 0.1 per cent by weight, preferably at least 0.2 per cent by weight, particularly at least 0.3 per cent by weight; and/or at most 10 per cent by weight, preferably at most 5 per cent by weight, particularly at most 3 per cent by weight.

The preferred use of the present invention is in the preparation of the vaccinating agent 21 from two vaccines, particularly preferably the preparation of a vaccinating agent 21 for use in the in particular simultaneous immunisation against Porcine Circovirus Disease "PCVD" and/or Enzootic Pneumonia "EP" or against infection with Porcine Circovirus and/or with Mycoplasma bacteria, preferably for use in immunisation against the disease Porcine Circovirus Disease "PCVD" and Enzootic Pneumonia "EP" or against infection with Porcine Circovirus, particularly type 2, and with Mycoplasma bacteria, particularly Mycoplasma hyopneumoniae. Moreover, the present invention relates primarily to vaccinating agents for veterinary medicine, particularly for use in pigs.

However, the present invention is not restricted to this combination. In particular, it is possible to use the proposed kit with other starting materials, particularly vaccines or antigens, such as for example with antigens of the pathogens described above. Here, too, it may be possible to achieve similar advantages at least in respect of ease of use and especially hygienic use. The same also applies to the aspect of the present invention that the vaccinating agent 21 prepared has a different colour from the starting materials 7,10, thus providing an efficient, simple and effective method of checking that the vaccinating agent 21 has been successfully prepared. The specific colour of the vaccinating agent may result for example from mixing the differently coloured starting materials 7 and 10. For example, mixing a yellow starting material 7 with a red starting material 10 leads to a vaccinating agent 21 that is orange in colour. The use of the first container 1 with an injection device 22 may also be applied successfully and advantageously to other fields, wherein similar advantages may be achieved particularly in respect of improved hygiene and/or reduced use of materials. However, it is particularly preferable to combine the proposed kit with a characteristic colour for the vaccinating agent 21 prepared which is different from the colours of the starting materials 7,10. This results in an exceptionally high degree of certainty in use. However, the individual aspects of the present invention may also be combined in any other desired manner. - 21 -

Reference numerals: 1 first container 2 wall 5 3 opening region 4 flange 5 closure device 6 clamping element 7 first starting material 10 8 gas 9 second container 10 second starting material 11 wall 12 opening region 15 13 flange 14 closure device 15 clamping element 16 gas 17 adapter device 20 18 adapter element 19 fluid channel 20 venting and/or exhaust device 21 vaccinating agent 22 injection device 25 23 receptacle 24 living creature

Claims

1. A process for preparing a vaccinating agent from a first starting material in a first container and a second starting material in a second container, wherein the second starting material is different from the first starting material, and wherein said vaccinating agent is used for the simultaneous immunisation of a subject against the diseases Porcine Circovirus Disease "PCVD" and Enzootic Pneumonia "EP", wherein the first starting material and the second starting material are liquid, the first starting material comprises a first of the components of a Mycoplasma vaccine and a Circovirus vaccine, the second starting material comprises the other components of the Mycoplasma vaccine and Circovirus vaccine, the total volume of the first container exceeds the volume of the first starting material at least by the volume of the second material, wherein the first container also contains a gas, wherein the volume of the gas exceeds the volume of the second starting material by at least 2 % by volume, wherein between a first container only partly filled with the first starting material and a second container comprising the second starting material a fluid connection is formed by an adapter device, such that, by means of the adapter device, when at least one factory provided closure device of at least one of the containers is pierced for the first and/or only time a fluid connection is formed between the first and second container, and the second starting material is conveyed through the adapter device and the closure device into the first container, and in the first container the vaccinating agent is formed from the first and second starting material.

2. The process according to claim 1, characterised in that the closure devices of both containers are penetrated with the adapter device.

3. The process according to claim 1 or claim 2, characterised in that the closure device of the second container and then the closure device of the first container is penetrated by the adapter device or vice versa.

4. The process according to any one of claims 1 to 3, characterised in that a fluid connection is provided between the containers such that the second starting material passes from the second container into the first container under the effect of gravity.

5. The process according to any one of claims 1 to 4, characterised in that the first container is moved during and/or after the transfer of the second starting material into the first container, so as to achieve or speed up a homogeneous reaction, particularly dissolving or mixing; and/or that the first container is placed in or on an injection device; and/or that the first container is placed in or on a multiple-use injection device, particularly an injection gun, pressure injector and/or self-filling syringe.

6. A kit when used according to the process of any one of claims 1 to 5 to immunise a subject against the diseases Porcine Circovirus Disease "PCVD" and Enzootic Pneumonia ΈΡ", the kit comprising: a first starting material and a second starting material, wherein the second starting material is different from the first starting material; a first container only partly filled with the first starting material; and a second container comprising the second starting material, wherein the first starting material and the second starting material are liquid, the first starting material comprises a first of the components of the Mycoplasma vaccine and Circovirus vaccine, the second starting material comprises the other components of the Mycoplasma vaccine and Circovirus vaccine, and the total volume of the first container exceeds the volume of the first starting material at least by the volume of the second material, wherein the first container also contains a gas, wherein the volume of the gas exceeds the volume of the second starting material by at least 2 % by volume, and wherein at least one of the containers is closed off with a factory provided closure device and the second container is connectable to the first container by means of an adapter device by piercing the closure device for the first and/or only time, such that the second starting material enters the first container and there forms the vaccinating agent with the first starting material.

7. The kit according to claim 6, characterised in that the first starting material comprises a first vaccine and the second starting material comprises a second vaccine different from the first vaccine.

8. The kit according to claim 6, characterised in that the first starting material comprises a first of the components of the Mycoplasma vaccine and Circovirus vaccine, and that the second starting material comprises the other components of the Mycoplasma vaccine and Circovirus vaccine.

9. The kit according to any one of claims 6 to 8, characterised in that the second starting material comprises at least one of the components of each of the Mycoplasma vaccine and Circovirus vaccine in amounts of more than 30 % by weight of total vaccine components.

10. The kit according to any one of claims 6 to 9, characterised in that the first starting material, the second starting material and/or the vaccinating agent is a suspension comprising vaccines and/or insoluble proteins.

11. The kit according to any one of claims 6 to 10, characterised in that the ratio by volume of the first starting material to the second starting material is between 3:1 and 1:3.

12. The kit according to any one of claims 6 to 11, characterised in that the vaccinating agent has a characteristic colour different from the two starting materials; and/or in that the vaccinating agent has a colour or no colour, in contrast to at least one of the starting materials.

13. The kit according to any one of claims 6 to 12, characterised in that the vaccinating agent is designed to prevent pigs from falling ill with Mycoplasma hyopneumoniae and/or Porcine Circovirus type 2.

14. The kit according to any one of claims 6 to 13, characterised in that at least one of the starting materials and/or the vaccinating agent comprises a polymeric adjuvant.

15. The kit according to claim 14, wherein the polymeric adjuvant is carbomer.

16. The kit according to any one of claims 6 to 15, characterised in that the first starting material contains water in a concentration of at least 20 % by weight, and wherein the first starting material contains one or more excipients, preservatives, antioxidants and/or emulsifiers in a concentration of at least 0.1 % by weight.

17. The kit of claim 16, wherein the first starting material contains water between 40 % and 60 % by weight and wherein the concentrations of total excipients, preservatives, antioxidants and emulsifiers is between 0.3 % and 3 % by weight.

18. The kit according to any one of claims 6 to 17, characterised in that the first container is filled with the first starting material in an amount of less than 70 % of the total volume of the first container.

19. The kit according to any one of claims 6 to 18, characterised in that the adapter device comprises a fluid channel for providing a fluidic connection between the inner spaces formed by the containers, wherein the adapter device comprises a venting or exhaust channel in addition to the fluid channel of the adapter device, particularly parallel thereto.

20. The kit according to claim 19, characterised in that one opening of the channel for venting or exhaust is set back, in respect of the outlet opening of the fluid channel on the side facing the first container, in the direction of the main extent of the adapter device; and/or an opening of the channel for venting or exhaust facing the second container is arranged on the side of the outlet opening of the fluid channel facing the second container, which faces the second container, facing the open end of the adapter device.

21. The kit according to any one of claims 6 to 20, characterised in that the first container, the second container and the adapter device form a sealed assembly, preferably with a common packaging; and/or that the first container can be used in or with a preferably multiple-use injection device, particularly an injection gun, pressure injector and/or self-filling syringe.

22. Use of a kit according to any one of claims 6 to 19, for producing and/or preparing a vaccinating agent, for simultaneous immunisation against the diseases Porcine Circovirus Disease "PCVD" and Enzootic Pneumonia "EP".