PiaSky advances C5 inhibition through innovative recycling technology, which enables its monthly SC administration
This partnership aims to accelerate research and development into innovative treatments and, if successful, will generate milestones and royalties
Third approval in China for AstraZeneca and Daiichi Sankyo’s Enhertu in less than two years
CN201 is a next generation CD3xCD19 bispecific antibody that augments and diversifies Merck’s pipeline, with potential applications in B-cell malignancies and autoimmune diseases
This accelerates the clinical-to-commercial process timeline and enables customers to develop the right molecule
To co-develop and co-commercialize MK-6070, an investigational delta-like ligand 3 (DLL3) targeting T-cell engager, worldwide except for Japan where Merck retains exclusive rights
The successful completion of the global Phase 3 trials paves the way to obtain marketing approval in the U.S. and EU
Approval is based on data from two Phase III studies in branch and central retinal vein occlusion (RVO) showing early and sustained vision improvements non-inferior to aflibercept
Dr. Reddy's had previously received the EU GMP certificate for its Rituximab drug substance
Shilpa Biologicals has developed high concentration adalimumab (100 mg/mL)
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