CA31447P1009 - Common Stock - After market: 9.97 0 (0%)
NASDAQ:FENC (2/7/2023, 7:00:01 PM)+0.26 (+2.68%)
GICS Sector | Health Care | ||
GICS Industry | Biotechnology |
Valuation | Growth | ||
Profitability | Health | ||
Dividend |
Earnings (Last) | 11-11 2022-11-11/bmo | Earnings (Next) | 02-27 2023-02-27/amc |
Ins Owners | 1.51% | Inst Owners | 43.3% |
Market Cap | 261.82M | Shares | 26.26M |
PE | N/A | Fwd PE | N/A |
Dividend Yield | N/A | Analysts | 83.33 |
IPO | 06-05 2001-06-05 |
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Fennec Pharmaceuticals, Inc. operates as a biopharmaceutical company. The company is headquartered in Research Triangle Park, North Carolina and currently employs 10 full-time employees. The company went IPO on 2001-06-05. The firm is focused on the development of PEDMARK for the prevention of platinum-induced ototoxicity in pediatric cancer patients. The Company’s only product candidate in the clinical-stage of development is PEDMARK. The company announced two results of Phase III clinical trials for the prevention of cisplatin induced hearing loss, or ototoxicity in children, including the pivotal Phase III study SIOPEL 6 and the proof-of-concept Phase III study in collaboration with the Children’s Oncology Group (COG ACCL0431). PEDMARK has the potential to reduce the incidence and/or grade of chemotherapy-induced hearing loss. The Company’s four subsidiaries includes Oxiquant, Inc. and Fennec Pharmaceuticals, Inc., both Delaware corporations, Cadherin Biomedical Inc., a Canadian company, and Fennec Pharmaceuticals (EU) Limited (Fennec Limited), an Ireland company. Apart from Fennec Pharmaceuticals, Inc., all subsidiaries are inactive.
FENNEC PHARMACEUTICALS INC
PO Box 13628, 68 Tw Alexander Dr
RESEARCH TRIANGLE PARK NORTH CAROLINA 27709
P: 19196364530.0
CEO: Rostislav Raykov
Employees: 10
Website: http://fennecpharma.com/
Fennec Pharma (FENC) announced Tuesday that the FDA granted the Orphan Drug Designation for its ear toxicity therapy Pedmark. Read the full story here.
~ PEDMARK® is the First and Only FDA-Approved Therapy Indicated to Reduce the Risk of Ototoxicity Associated with Cisplatin in Pediatric Patients with...
Fennec Pharma (FENC) rose Wednesday morning after announcing that the National Comprehensive Cancer Network ((NCCN)) recommended its ear toxicity therapy Pedmark. Read the full story here.
~ PEDMARK is the First and Only FDA-Approved Therapy Indicated to Reduce the Risk of Ototoxicity Associated with Cisplatin in Pediatric Patients with...
~ In September 2022, FDA Approved PEDMARK®, the First and Only FDA-Approved Therapy Indicated to Reduce the Risk of Ototoxicity Associated with Cisplatin...
~ PEDMARK is the First and Only FDA-Approved Therapy Indicated to Reduce the Risk of Cisplatin-Induced Hearing Loss in Pediatric Patients ~ ~ Fennec...
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