Rocket Pharmaceuticals Announces First Patient Treated in Global Registrational Phase 2 Study of RP-L102 “Process B” for Fanconi Anemia
Rocket Pharmaceuticals, Inc. (RCKT)
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Source: Business Wire
—Preliminary Phase 2 Data Anticipated in 2020— NEW YORK--(BUSINESS WIRE)--Rocket Pharmaceuticals, Inc. (NASDAQ: RCKT) (“Rocket”), a clinical-stage company advancing an integrated and sustainable pipeline of genetic therapies for rare childhood disorders, today announces that the first patient in the global Phase 2 registration-enabling study of RP-L102 “Process B” received investigational therapy. RP-L102 is the Company’s lentiviral vector (LVV)-based gene therapy for the treatment of Fanconi Anemia (FA).“The initiation of Rocket’s first Phase 2 trial is an important milestone for the company as well as patients throughout the world battling FA,” said Kinnari Patel, Pharm.D., MBA, Chief Operating Officer and Head of Development of Rocket. “With the recent feedback received from the FDA and EMA of MMC-resistance as the primary endpoint, we are optimistic about the prospect of benefiting patients and, if the data are positive, working towards BLA and MAA submissions.”The registration
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News
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RCKT
Earnings
- 8/5/24 - In-Line
RCKT
Sec Filings
- 11/4/24 - Form 4
- 11/4/24 - Form 4
- 10/31/24 - Form 144
- RCKT's page on the SEC website