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Merck said that the review findings of the clinical trials showed that V590 and V591 were generally well tolerated, but the immune responses were inferior to those seen

Through the expanded agreement, Humanigen will now gain access to manufacturing capacity reserved by the Biomedical Advanced Research and Development Authority (BARDA) for the development of lenzilumab as

The Sputnik V vaccine was registered under the emergency use authorisation procedure based on the results from the Russian Phase III clinical trials on more than 33,000 people.

The rapidly fast-spreading B.1.1.7 lineage, a variant strain of SARS-CoV-2 detected initially in the UK, has ten mutations located in the spike protein. The two firms had earlier

Akron Biotech will produce the Human AB Serum using Octapharma’s solvent-detergent treated human plasma, Octaplas. The Octaplas viral inactivation and production process includes several independent and complementary steps

As part of the development, Gritstone and the National Institute of Allergy and Infectious Diseases (NIAID), part of the National Institutes of Health, have signed an agreement to

Novartis and GSK have agreed to provide £2.8m ($3.6m) for the Africa Genomic Research Approach for Diversity and Optimizing Therapeutics (GRADIENT) project (Project Africa GRADIENT), over the next

The companies will leverage Cure Genetics’ VELP platform to develop the vectors. Under the partnership, Boehringer’s experience in disease biology and gene therapy development will be combined with

Etana now has the right to sell BYVASDA in the country and in return, Innovent Biologics will receive milestones for the development and commercialisation along with double-digit royalties