GenSight Biologics gets early access nod for candidate gene therapy in Israel
Applications include detailed scientific rationale and supporting clinical evidence
Applications include detailed scientific rationale and supporting clinical evidence
The interim efficacy readout, involving around 170 participants with 15-month data, remains on track for the end of March 2026
The company also revealed that MK-2214 has received Fast Track Designation from the U.S. Food and Drug Administration
The hospital has already onboarded 200+ experienced doctors and is expected to generate 5,000–7,000 jobs
CD388 is administered as a single 450-milligram subcutaneous dose in adults and adolescents
Pfizer and Valneva have been collaborating on VLA15’s development and commercialization since April 2020
The proposed transaction will be effected as a share swap
Consolidated revenue from operations stood at Rs. 111.05 crore
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