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Approval is based on GMMG-HD7 phase 3 study for those who are transplant-eligible, newly diagnosed with multiple myeloma.
By: Rachel Klemovitch
Will gain access to Vicebio’s Molecular Clamp technology, which enables development of next-gen multivalent vaccines against respiratory pathogens.
By: Charlie Sternberg
A cornerstone of the investment is a proposed new drug substance manufacturing center focused on chronic diseases in the Commonwealth of Virginia.
Thermo Fisher to acquire Sanofi’s steriles manufacturing site in Ridgefield, NJ and continue to manufacture a portfolio of therapies for Sanofi.
Welcomes Brian Riley as President and Chief Technical Officer, Joanne Lager, MD as Chief Medical Officer, and Adrian Chaisson as Chief of Staff.
Sanofi plans to explore the oral dual JAK/SYK inhibitor’s potential in a new indication not previously studied through a phase 1 study.
Expands portfolio in rare immunological disease and adds early-stage pipeline in immunology
The CDMO's head of development talks about ADCs, accelerated timelines, and the push for end-to-end development services.
By: Tim Wright
The acquisition enhances Sanofi’s early-stage pipeline and includes VG-3927.
The BLA approval was based on pivotal Phase 3 clinical trial data that showed Nuvaxovid was safe and effective for the prevention of COVID-19.
Will boost manufacturing and research & development efforts in the country.
Törnsén has 20+ years of experience across global and U.S. operations, where she held multiple senior commercial leadership roles.
Xavier Jacq is a scientist with extensive experience in small molecule drug development and mitochondrial biology.
Dupixent is already approved for CSU in Japan, the United Arab Emirates, and Brazil.
New appointments will provide the company with broader expertise in regulatory affairs, clinical development and commercialization.
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