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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.
By: Charlie Sternberg
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.
By: Rachel Klemovitch
New appointments will provide the company with broader expertise in regulatory affairs, clinical development and commercialization.
Aims to accelerate the development of HXN-1002 and HXN-1003.
Novartis cuts approximately 430 employees from East Hanover HQ, and 34 employees in San Diego.
By: Kristin Brooks
Following a promising pre-clinical program, Sanofi is planning a phase 1/2 randomized, clinical study.
DR-0201 is being evaluated in two ongoing phase 1 studies and has shown deep and robust B-cell depletion in non-clinical and clinical settings.
Mederia boasts 3+ decades of leadership in biopharmaceutical manufacturing, most notably in pioneering exosome production.
Villemagne previously served as CEO of Carbogen Amcis.
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