iRegene doses first US Parkinson’s patient, launches landmark MSA trial in China
The move follows encouraging Phase I data and a series of regulatory wins from the U.S. Food and Drug Administration
The move follows encouraging Phase I data and a series of regulatory wins from the U.S. Food and Drug Administration
The program offers selected participants advanced access to Promise Bio’s broad-epiproteomic platform
The decision follows compelling data from the AMPLIFY Phase III trial, demonstrating that 77% of patients receiving the Calquence-venetoclax combination were progression-free at three years
This multi-year CDMO agreement involves significant, ongoing manufacturing for a global pharmaceutical major
The approval, based on results from the Phase 3 AMPLIFY trial, marks the first all-oral, fixed-duration regimen for first-line CLL therapy
Bosentan 32 mg tablets for oral suspension are indicated for the treatment of Pulmonary Arterial Hypertension
The enhancements will improve environmental sustainability, strengthen material governance, and boost utility reliability
The recommendation is based on new data from continuous safety monitoring of medicines in the EU
Ind-Ra expects chronic therapies to outpace IPM as compliance improves and lifestyle diseases rise
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