Glenmark initiates multi-country Phase 3 clinical trial for Envafolimab in resectable Stage III NSCLC
The company has received approval from DCGI to begin patient enrolment and dosing in the country
The company has received approval from DCGI to begin patient enrolment and dosing in the country
Bain Capital and Cinven will each retain a minority stake, reflecting their ongoing confidence in STADA’s future growth
The medicine was well tolerated, with no unexpected safety issue
This is Lupin's first product using proprietary Nanomi's technology and has a 180-day CGT exclusivity
Milrinone is indicated for the short-term intravenous treatment of patients with acute decompensated heart failure
Brenntag Specialties will provide pharmaceutical manufacturers and biopharmaceutical companies with a reliable supply of high-purity, GMP-compliant acetates
Phase 1 has a total reactor capacity of 440 kL with 63 reactors
Glenmark’s Eribulin Mesylate Injection, 1 mg/2 mL (0.5 mg/mL) Single-Dose Vials is bioequivalent and therapeutically equivalent to the reference listed drug, Halaven Injection, 1 mg/2 mL (0.5 mg/mL),of Eisai
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