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Dynavax, US Department of Defense collaborate to develop recombinant plague vaccine adjuvanted with CpG 1018

Emeryville, California
Tuesday, October 5, 2021, 16:00 Hrs  [IST]

Dynavax Technologies Corporation, a biopharmaceutical company focused on developing and commercializing vaccines, and the US Department of Defense (DOD) announced Dynavax has executed an agreement for approximately $22 million over two and a half years to develop a recombinant plague vaccine adjuvanted with CpG 1018.  

Under the agreement, Dynavax will conduct a phase 2 clinical trial combining its CpG 1018 adjuvant with the DOD's rF1V vaccine.  The company anticipates the phase 2 trial will commence in 2022.

Ryan Spencer, Dynavax's chief executive officer commented, "We are honored to receive this award and to support the US government in developing a plague vaccine to protect the US military members who put their lives at risk every day in service to the country.  The development of a CpG 1018 adjuvanted plague vaccine is an important example of the broad utility of our adjuvant which we are leveraging to build our pipeline of new and improved vaccines. Our confidence in CpG 1018 is built on the successful development of our FDA-licensed 2-dose adult hepatitis B vaccine and the multiple late-stage Covid-19 vaccine candidates utilizing CpG 1018."

This agreement, funded by the DOD's Joint Program Executive Office for Chemical, Biological, Radiological and Nuclear Defense's (JPEO-CBRND) Joint Project Manager for Chemical, Biological, Radiological, and Nuclear Medical (JPM CBRN Medical), enables Dynavax to conduct a phase 2 clinical trial, submit an Investigational New Drug (IND) application to the US Food and Drug Administration (FDA), and generate additional clinical trial results to add to the existing clinical and non-clinical data. Any future commercial supply agreements would be subject to a separate agreement between Dynavax and the US government.

COL Ryan Eckmeier, the joint project manager for CBRN Medical commented, "Advancing the development of a recombinant plague vaccine supports the JPM CBRN Medical's vision to deliver a full, layered medical countermeasure capability to enable a protected and unencumbered Joint Force to fight and win in any global CBRN battlespace. Incorporating the CpG 1018 adjuvant to the DOD's rF1V vaccine will hopefully allow us to protect our service members with fewer doses administered over a shorter time period."

The planned phase 2 randomized, placebo-controlled, observer-blind, multicenter clinical trial will evaluate the immunogenicity, safety, and tolerability of the rF1V vaccine antigens provided by the US government combined with Dynavax's CpG 1018 adjuvant in adults 18 to 55 years of age.

CpG 1018 is the adjuvant used in HEPLISAV-B. Dynavax developed CpG 1018 adjuvant to provide an increased vaccine immune response, which has been demonstrated in HEPLISAV-B. CpG 1018 adjuvant provides a well- developed technology and a significant safety database, potentially accelerating the development and large-scale manufacturing of a Covid-19 vaccine.

Dynavax is a commercial stage biopharmaceutical company developing and commercializing novel vaccines.

 

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