Services do NOT include

Please contact the service provider to discuss details.

Possible Output

Summary of results. A detailed report of the study results will be provided by VFI to the user, as well as adjuvanted formulations for use in in vivo studies. Please feel free to contact us before applying to the service to discuss feasibility and outline of the study.

Sample Requirements - input of users

Various. To be discussed before starting.

Lead Scientist

Dr. Thomas Courant

Adjuvant and formulation services

Description of service

The Vaccine Formulation Institute (VFI) offers formulation studies of vaccine antigens with adjuvants. VFI adjuvants include SWE, an oil-in-water emulsion available at GMP grade, and combination adjuvants (emulsions and liposomes QS21 saponin and/or TLR agonists). Aluminum salts and dmLT adjuvants can also be included in formulation studies. The vaccine antigen is usually provided to VFI by the applicant. Formulations are tested at the VFI for compatibility, stability and antigen integrity (conditional to the transfer of method and / or reagents to VFI) determining their suitability for in vivo use. A detailed report of the study results will be provided by VFI to the user, as well as adjuvanted formulations for use in in vivo studies. Please feel free to contact VFI before applying to the service to discuss feasibility and outline of the study.

Timeline 

Project duration approximately 2 months

Contact 

Dr. Maria Lawrenz

maria.lawrenz@vformulation.org 

004917663070618

Cost coverage opportunities

If you are interested in this service please contact the service provider directly 

Free 

This project has received funding from the European Union's Horizon 2020 research and innovation programme under grant agreement N° 730964.

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