The randomized, double-blind, placebo-controlled Phase 1 study is designed to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of BGE-102 in healthy participants
Fourteenth breakthrough therapy designation granted by FDA across the oncology portfolio of Daiichi Sankyo
Phase 1 dosing is expected to finish by the end of 2025
The company reported revenue from operations at Rs. 6,573.7 crore, up 6 per cent YoY
NorUDCA is the first?in?class treatment for Non?alcoholic Fatty Liver Disease (NAFLD) in India
Vasograin Plus represents a major advancement in the treatment of migraine
India Formulation sales accounted for 34.2% of total consolidated sales for the quarter
He most recently served as Chief Medical Officer of AstraZeneca and Alexion
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