Lantern Pharma’s Investigational Drug-Candidate, LP-184, Receives Fast-Track Designation in Glioblastoma from the FDA
Lantern Pharma Inc. (LTRN)
Company Research
Source: Business Wire
Fast Track Designation is designed to expedite FDA review of important new drugs to treat serious conditions and fill an unmet medical need.Fast Track Designation for LP-184 (STAR-001) recognizes Glioblastoma (GBM) as a serious condition impacting more than 13,000 U.S. adults each year and approximately 300,000 globally.A phase 1b/2a clinical trial for recurrent GBM is targeted to start in late 2024/early 2025.LP-184, which will be developed as STAR-001 for CNS and other neuro-oncology indications by Starlight Therapeutics, a wholly owned subsidiary of Lantern Pharma, has the potential to be the first new drug for treating GBM in more than 20 years. DALLAS--(BUSINESS WIRE)--Lantern Pharma Inc. (NASDAQ: LTRN), an artificial intelligence (AI) company dedicated to developing cancer therapies and transforming the cost, pace, and timeline of oncology drug discovery and development, today announced that the FDA has granted Fast Track Designation for investigational drug candidate, LP-184
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- Lantern Pharma Reports Third Quarter 2024 Financial Results and Business UpdatesBusiness Wire
- Starlight Therapeutics Announces Inaugural Members of Scientific Advisory BoardBusiness Wire
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