DR. REDDY'S LABORATORIES, INC.

Clinical Trials
2
Trial Phases
1 Phases
Drug Approvals
156
Drug Approvals
- Prev
- 1
- 2
- 3
- 4
- 5
- 13
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Clinical Trials
Distribution across different clinical trial phases (2 trials with phase data)• Click on a phase to view related trials
News
Dr. Reddy's and Alvotech Partner to Develop Keytruda Biosimilar in $29.5 Billion Market
Dr. Reddy's Laboratories and Alvotech have entered a collaboration and license agreement to co-develop, manufacture, and commercialize a biosimilar version of Keytruda (pembrolizumab) for global markets.
Eisai and Merck Secure Patent Victory, Blocking Lenvima Generic Until 2036
Eisai and Merck successfully defended a key patent for cancer drug Lenvima against Shilpa Medicare's challenge, with a federal judge ruling the patent describes the invention clearly and in sufficient detail.
USFDA Issues Form 483 with Two Observations for Dr. Reddy's New York API Facility
The U.S. Food and Drug Administration completed a Good Manufacturing Practice inspection at Dr. Reddy's Middleburgh API facility in New York, resulting in two observations via Form 483.
Esperion Secures Patent Protection for NEXLETOL Until 2040 Through Settlement with Micro Labs
Esperion Therapeutics has reached a settlement agreement with Micro Labs that prevents the generic manufacturer from marketing a version of NEXLETOL (bempedoic acid) before April 19, 2040.
Ingenus Pharmaceuticals Advances Cancer Drug Patent Suit Against Nexus, Court Dismisses Co-Plaintiff
A federal judge in Illinois ruled that Ingenus Pharmaceuticals can proceed with its patent infringement lawsuit against Nexus Pharmaceuticals regarding cyclophosphamide liquid formulations used in cancer treatment.
Dr. Reddy's to Launch Sanofi's Beyfortus in India for RSV Prevention in Infants
Dr. Reddy's Laboratories has secured exclusive rights to promote and distribute Sanofi's novel RSV drug Beyfortus (nirsevimab) in India, expanding their existing vaccine partnership.
FDA Approves 25 First-Time Generic Drugs in First Half of 2025, Expanding Access to Critical Therapies
The FDA approved 25 first-time generic drugs in the first six months of 2025, including generics for critical medications treating HIV, cancer, and neurological conditions.
Real-World Studies Confirm Bevacizumab Biosimilars Deliver Cost Savings and Equivalent Clinical Outcomes in Metastatic Colorectal Cancer
A Canadian population-based study found bevacizumab biosimilars Mvasi and Zirabev provided $6,379 CAD in annual cost savings per patient compared to originator Avastin while maintaining equivalent survival outcomes in metastatic colorectal cancer.
Novo Nordisk Plans India Entry for Ozempic Despite Looming Patent Expiry as Indian Pharma Giants Prepare Generic Alternatives
Danish pharmaceutical giant Novo Nordisk confirms readiness to launch its blockbuster GLP-1 drug Semaglutide (Ozempic) in India despite patent expiration in January 2026, emphasizing continued market leadership strategy.
Rigel Pharmaceuticals Reports Strong Growth with TAVALISSE and REZLIDHIA in 2024, Expands Global Reach
Rigel Pharmaceuticals achieved significant revenue growth in 2024, with TAVALISSE sales increasing 12% to $104.8 million and REZLIDHIA sales growing 118% to $23.0 million.