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Abpro Forms Strategic Partnership to Advance Two Bispecific Antibody Candidates in Asian Markets

Abpro, a biotechnology company dedicated to developing next-generation antibody therapeutics to improve the lives of patients with severe and life-threatening diseases, announced the formation of a strategic partnership to advance two bispecific antibodies in key Asian markets including Greater...

FDA approves GSKs Advil Dual Action with Acetaminophen for over-the-counter use in the United States

GlaxoSmithKline announced that the U.S. FDA has approved Advil Dual Action with Acetaminophen as an over-the-counter (OTC) product for pain relief. The exclusive formula is now the first FDA-approved OTC combination of ibuprofen and acetaminophen in the United States...

Catalent Announces Supplying Blueprint Medicines Precision Therapy AYVAKIT

Catalent, the leading global provider of advanced delivery technologies, development, and manufacturing solutions for drugs, biologics, gene and cell therapies, and consumer health products, welcomes the announcement by Blueprint Medicines Corporation that the U.S. Food and Drug Administration (FDA)...

Rare Disease Patient Platform Raremark Partners With TriNetX

TriNetX, the global health research network that revolutionizes clinical research and enables discoveries through the generation of real-world evidence (RWE), announced that Raremark, a patient-data platform focused on rare disease, has partnered with the TriNetX network to bring more...

Signant Health invests for growth with the opening of its new Philadelphia-area office

Signant Health, an industry-leading clinical research technology and solutions company, is proud to announce that it has officially opened a new, leading edge office facility in Blue Bell, Pennsylvania. Construction on the new office, which is the largest workplace...

Sun Pharma Launches RIOMET ER Oral Suspension in the U.S.

Sun Pharmaceutical Industries Ltd. announced that one of its whollyowned subsidiaries has launched Riomet ERâ„¢ in the U.S. as an adjunct to diet and exercise to improve glycemic control in patients 10 years of age and older with type...

Dulaglutide Receives FDA Approval for Reducing MACE in Type 2 Diabetics

The U.S. FDA has approved Trulicity® (dulaglutide) for the reduction of major adverse cardiovascular events (MACE) in adults with type 2 diabetes who have established cardiovascular (CV) disease or multiple cardiovascular risk factors. This decision makes Eli Lilly and...

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