FDA Clears IND for Mustang Bio’s MB-102 (CD123 CAR T)
Mustang Bio, Inc. (MBIO)
Last mustang bio, inc. earnings: 11/12 07:30 am
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mustangbio.com/investor-relations
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Source: GlobeNewswire
NEW YORK, Aug. 05, 2019 (GLOBE NEWSWIRE) -- Mustang Bio, Inc. (“Mustang”) (NASDAQ: MBIO), a clinical-stage biopharmaceutical company focused on translating today’s medical breakthroughs in cell and gene therapies into potential cures for hematologic cancers, solid tumors and rare genetic diseases, today announced that the U.S. Food and Drug Administration (FDA) has approved the Company’s Investigational New Drug (IND) application to initiate a multi-center Phase 1/2 clinical trial of MB-102 (CD123 CAR T) in acute myeloid leukemia (AML), blastic plasmacytoid dendritic cell neoplasm (BPDCN) and high-risk myelodysplastic syndrome (MDS). MB-102 is a CAR T cell therapy that is produced by engineering patient T cells to recognize and eliminate CD123-expressing tumors. CD123 is widely expressed on bone marrow cells of patients with myelodysplastic syndrome and hematologic malignancies, including in 75-89% of AML patients and over 90% in BPDCN patients. MB-102 has shown promising response
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MBIO
News
- Mustang Bio Receives Positive Listing Determination from NasdaqGlobeNewswire
- Mustang Bio Granted Orphan Drug Designation by U.S. FDA for MB-108 (HSV-1 oncolytic virus) to Treat Malignant GliomaGlobeNewswire
- Mustang Bio Secures $4M through Strategic Warrant Agreement [Yahoo! Finance]Yahoo! Finance
- Mustang Bio Announces Exercise of Warrants for $4 Million Gross ProceedsGlobeNewswire
MBIO
Sec Filings
- 12/6/24 - Form DEF
- 12/2/24 - Form 424B3
- 11/29/24 - Form EFFECT
- MBIO's page on the SEC website