1. Show article details.

    BRIEF-Fennec Pharmaceuticals Announces Up To $45 Mln Investment From Petrichor

    Reuters – 7:36 AM ET 08/01/2022

    Fennec Pharmaceuticals Inc (FENC): * FENNEC PHARMACEUTICALS ANNOUNCES UP TO $45 MILLION INVESTMENT FROM PETRICHOR Source text for Eikon: Further company coverage:

  2. Show article details.

    Fennec Pharmaceuticals Announces Up to $45 Million Investment From Petrichor

    GlobeNewswire – 7:30 AM ET 08/01/2022

    ~ Under the Terms of the Investment Agreement, $5 Million to be Funded on initial closing and $20 Million to be Funded Upon Potential FDA Approval of PEDMARKTM ~ ~ Fennec Has the Potential to Access an Additional $20 Million Prior to December 31, 2023 ~ ~ Funding to Support the Potential Commercialization of PEDMARKTM to Reduce the Risk of Ototoxicity Associated with Cisplatin in Pediatric Pati...

  3. Show article details.

    Fennec Announces Results of Annual Meeting

    GlobeNewswire – 6:00 PM ET 06/14/2022

    Fennec Pharmaceuticals Inc. (FENC) today announced that the nominees listed in the management proxy circular dated April 20, 2022 for the Annual General Meeting of Shareholders were elected as directors of the Company at the Annual General Meeting of Shareholders held in New York, New York on June 14, 2022.

  4. Show article details.

    Fennec Pharmaceuticals to Participate in Upcoming Investor Conferences

    GlobeNewswire – 7:29 AM ET 05/23/2022

    Fennec Pharmaceuticals Inc. (FENC), a specialty pharmaceutical company focused on the development of PEDMARKTM  for the prevention of platinum-induced ototoxicity in pediatric patients, today announced that the Company will be participating in upcoming conferences.

  5. Show article details.

    Fennec Pharmaceuticals Announces First Quarter 2022 Financial Results and Provides Business Update

    GlobeNewswire – 6:00 AM ET 05/12/2022

    ~ FDA Prescription Drug User Fee Act Target Action Date Set for September 23, 2022 ~ ~ If Approved by the FDA, PEDMARKTM Stands to Be the First Therapy for the Prevention of Cisplatin-Induced Hearing Loss in Children ~ ~ Company Has Approximately $18.3 Million in Cash and $5 Million of Funded Debt ~ RESEARCH TRIANGLE PARK, N.C., May 12, 2022 -- Fennec Pharmaceuticals Inc. (FENC), a specialty pharmaceu...

  6. Show article details.

    U.S. FDA accepts Fennec Pharma's New Drug Application (NDA) Resubmission for PEDMARK

    Benzinga – 8:39 AM ET 04/27/2022

    Fennec Pharmaceuticals Inc. announced that the U.S. Food and Drug Administration  has accepted for filing of resubmitted New Drug Application for PEDMARKTM  for the prevention of platinum-induced ototoxicity in pediatric patients one month to less than 18 years of age with localized, non-metastatic, solid tumors. The regulatory agency has set a target action date of September 23, 2022.

  7. Show article details.

    Fennec Pharmaceuticals Announces FDA Acceptance for Filing of New Drug Application Resubmission for PEDMARK™

    GlobeNewswire – 6:00 AM ET 04/27/2022

    Fennec Pharmaceuticals Inc. (FENC), a specialty pharmaceutical company, today announced that the U.S. Food and Drug Administration  has accepted for filing the Company’s resubmitted New Drug Application for PEDMARKTM (a unique formulation of sodium thiosulfate) for the prevention of platinum-induced ototoxicity in pediatric patients one month to <18 years of age with localized, non-metastatic, solid t...￿

  8. Show article details.

    Fennec Pharmaceuticals to Participate in the 2022 Maxim Virtual Growth Conference

    GlobeNewswire – 7:00 AM ET 03/25/2022

    Fennec Pharmaceuticals Inc. (FENC), a specialty pharmaceutical company focused on the development of PEDMARK™  for the prevention of platinum-induced ototoxicity in pediatric patients, today announced that the Company will be participating in the 2022 Maxim Group Virtual Growth Conference, taking place March 28-30, 2022.

  9. Show article details.

    The Daily Biotech Pulse: Novartis Prostate Cancer Drug Lands FDA Approval, Ligand Announces SPAC Deal To Spin Off Antibody Business, Lilly's Lung Cancer Therapy Hit With CRL

    Benzinga – 8:10 AM ET 03/24/2022

    Here's a roundup of top developments in the biotech space over the last 24 hours: Novartis AG said the U.S. Food and Drug Administration approved Pluvicto for the treatment of adult patients with a certain type of advanced cancer called prostate-specific membrane antigen-positive metastatic castration-resistant prostate cancer that has spread to other parts of the body.

  10. Show article details.

    Fennec Pharmaceuticals Resubmits New Drug Application to U.S. Food and Drug Administration for Pedmark™

    GlobeNewswire – 6:00 AM ET 03/24/2022

    Fennec Pharmaceuticals Inc. (FENC), a specialty pharmaceutical company, today announced the resubmission of its New Drug Application to the U.S. Food and Drug Administration  for PEDMARK™ (a unique formulation of sodium thiosulfate) for the prevention of platinum-induced ototoxicity in pediatric patients one month to <18 years of age with localized, non-metastatic, solid tumors.￿

  11. Show article details.

    Fennec Pharmaceuticals Announces Fiscal Year 2021 Financial Results And Provides Business Update

    GlobeNewswire – 6:00 AM ET 02/28/2022

    ~ Resubmission of NDA for PEDMARK™ Targeted for the First Quarter of 2022 ~ ~ Company has Approximately $21.1 Million in Cash and $5 Million of Funded Debt ~ Fennec Pharmaceuticals Inc. (FENC), a specialty pharmaceutical company focused on the development of PEDMARK™ (a unique formulation of sodium thiosulfate) for the prevention of platinum-induced ototoxicity in pediatric patients, today reported it...

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    FENC announced Q2 earnings.

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