Bristol Myers Squibb scores FDA priority review for Opdivo in advanced hodgkin lymphoma
The FDA aims to make a decision by April 8, 2026
The FDA aims to make a decision by April 8, 2026
Alport Syndrome is caused by genetic mutations affecting type IV collagen in the kidneys, ears, and eyes
The center will offer training to super-specialist doctors and healthcare professionals in various fields
The partnership aims to combine TQx’s in vivo therapeutic expertise with Kytopen’s continuous flow transfection technology
Ascelis Center of Excellence for Peptide Development and Characterization will drive the development of cosmetic, therapeutic, and pharmaceutical peptides
The update reflects long-term clinical trial data showing that many patients with mCSCC or laCSCC experienced lasting responses
SOMA Color Mind is designed to simplify and accelerate color setup directly on the printing press
Merus has licensed Halozyme’s proprietary ENHANZE technology to develop and commercialize subcutaneous formulations of petosemtamab
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