Cellectar’s CLR 131 Receives FDA Rare Pediatric Disease Designation for the Treatment of Ewing’s Sarcoma
Cellectar Biosciences, Inc. (CLRB)
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Source: GlobeNewswire
MADISON, Wis., Aug. 13, 2018 (GLOBE NEWSWIRE) -- Cellectar Biosciences (Nasdaq: CLRB), a clinical-stage biopharmaceutical company focused on the discovery, development and commercialization of drugs for the treatment of cancer, announces today that the U.S. Food and Drug Administration (FDA) has granted Rare Pediatric Disease Designation (RPDD) to CLR 131, the company’s lead Phospholipid Drug Conjugate™ (PDC) product candidate, for the treatment of Ewing’s sarcoma, a rare pediatric cancer. “We are delighted to announce receipt of our third RPDD from the FDA, which underscores Cellectar’s commitment to rare pediatric cancers. There is a critical need to develop new therapies to fight deadly childhood cancers such as Ewing’s sarcoma, and CLR 131 has shown early promise in this arena,” said John Friend, M.D., chief medical officer of Cellectar Biosciences. “This designation, combined with our receipt of FDA Orphan Drug Designation for Ewing’s sarcoma last month, will help support
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CLRB
Sec Filings
- 4/1/24 - Form 10-K/A
- 3/27/24 - Form 8-K
- 3/27/24 - Form 10-K
- CLRB's page on the SEC website