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2025-10-262026-04-19
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25 items- PRJourney Medical Corporation Secures Contract with Third Major GPO for Emrosi™SCOTTSDALE, Ariz., April 21, 2026 (GLOBE NEWSWIRE) -- Journey Medical Corporation (NASDAQ:DERM) ("Journey Medical" or "the Company", "we", or "our"), a commercial-stage pharmaceutical company primarily focused on developing, selling and marketing FDA-approved prescription pharmaceutical products for the treatment of dermatological conditions, today announced that approximately 85% of all commercial lives in the United States now have access to Emrosi™ (40 mg Minocycline Hydrochloride Modified-Release Capsules, 10 mg immediate release and 30 mg extended release) after contracting with the third major group purchasing organization (GPO). Emrosi™ is for the treatment of inflammatory lesions o
- INSIDERSEC Form 4 filed by Jin David4 - Fortress Biotech, Inc. (0001429260) (Issuer)
- SECSEC Form 10-K filed by Fortress Biotech Inc.10-K - Fortress Biotech, Inc. (0001429260) (Filer)
- SECFortress Biotech Inc. filed SEC Form 8-K: Results of Operations and Financial Condition, Financial Statements and Exhibits8-K - Fortress Biotech, Inc. (0001429260) (Filer)
- PRFortress Biotech Reports 2025 Financial Results and Recent Corporate HighlightsZYCUBO® approved by FDA to treat Menkes disease in the United States; Fortress subsidiary Cyprium Therapeutics sold its Rare Pediatric Disease Priority Review Voucher (PRV) for gross proceeds of $205 million; Cyprium is also eligible to receive tiered royalties and up to approximately $128 million in aggregate sales milestones from Sentynl Therapeutics Fortress subsidiary Checkpoint Therapeutics acquired by Sun Pharma; Fortress remains eligible to receive up to an additional $4.8 million under a contingent value right (CVR), plus a 2.5% royalty on net sales of UNLOXCYT™ (cosibelimab-ipdl) MIAMI, March 31, 2026 (GLOBE NEWSWIRE) -- Fortress Biotech, Inc. (NASDAQ:FBIO) ("Fortress"), an inno
- SECFortress Biotech Inc. filed SEC Form 8-K: Other Events, Financial Statements and Exhibits8-K - Fortress Biotech, Inc. (0001429260) (Filer)
- PRFortress Biotech's Subsidiary Cyprium Therapeutics Closes Sale of Rare Pediatric Disease Priority Review Voucher for $205 MillionMIAMI, March 30, 2026 (GLOBE NEWSWIRE) -- Fortress Biotech, Inc. (NASDAQ:FBIO) ("Fortress") and its majority-owned subsidiary, Cyprium Therapeutics, Inc. ("Cyprium"), today announced the closing of the sale of Cyprium's Rare Pediatric Disease Priority Review Voucher ("PRV") for gross proceeds of $205 million. "The sale of the PRV by Cyprium is a transformational corporate transaction for both Cyprium and Fortress. As the majority shareholder of Cyprium, Fortress expects to receive over $100 million in proceeds from the transaction, which will enhance our financial flexibility to invest in business development and the continued advancement of our robust portfolio," said Lindsay A. Rosenwal
- PRJourney Medical Corporation Reports Full-Year 2025 Financial Results and Recent Corporate HighlightsTotal revenues were $61.9 million in FY2025 compared to $56.1 million in FY2024 Emrosi™ generated net revenues of $14.7 million during the full-year period after its launch in early April 2025 Approximately 53,000 total prescriptions were filled for Emrosi™ during FY2025 Payer access for Emrosi™ available to over 100 million U.S. commercial lives Company to hold conference call today at 4:30 p.m. ET SCOTTSDALE, Ariz., March 25, 2026 (GLOBE NEWSWIRE) -- Journey Medical Corporation (NASDAQ:DERM) ("Journey Medical," "the Company," "we" or "our"), a commercial-stage pharmaceutical company focused on developing, selling and marketing FDA-approved prescription pharmaceutical products for t
- SECAmendment: SEC Form SCHEDULE 13D/A filed by Fortress Biotech Inc.SCHEDULE 13D/A - Fortress Biotech, Inc. (0001429260) (Subject)
- INSIDERSEC Form 4 filed by Rosenwald Lindsay A Md4 - Fortress Biotech, Inc. (0001429260) (Issuer)
- INSIDERSEC Form 4 filed by Weiss Michael S4 - Fortress Biotech, Inc. (0001429260) (Issuer)
- PRJourney Medical Corporation to Announce Year End 2025 Financial Results on March 25, 2026SCOTTSDALE, Ariz., March 18, 2026 (GLOBE NEWSWIRE) -- Journey Medical Corporation ("Journey Medical" or the "Company") (NASDAQ:DERM), a commercial-stage pharmaceutical company primarily focused on selling and marketing U.S. Food and Drug Administration ("FDA")-approved prescription pharmaceutical products for the treatment of dermatological conditions, today announced the Company will release its year end 2025 financial results after the U.S. financial markets close on Wednesday, March 25, 2026. Journey Medical management will conduct a conference call and audio webcast on Wednesday, March 25, 2026 at 4:30 p.m. ET. To listen to the conference call, interested parties within the U.S. shoul
- PRUPDATE: Fortress Biotech's Subsidiary Cyprium Therapeutics Enters into Agreement to Sell Rare Pediatric Disease Priority Review Voucher for $205 MillionMIAMI, Feb. 23, 2026 (GLOBE NEWSWIRE) -- Fortress Biotech, Inc. (NASDAQ:FBIO) ("Fortress") and its majority-owned subsidiary, Cyprium Therapeutics, Inc. ("Cyprium"), today announced that Cyprium entered into a definitive asset purchase agreement to sell its Rare Pediatric Disease Priority Review Voucher ("PRV") for gross proceeds of $205 million upon the closing of the transaction. In December 2023, Sentynl Therapeutics, Inc. ("Sentynl") assumed full responsibility for the development and commercialization of ZYCUBO® (copper histidinate, formerly known as CUTX-101) from Cyprium. The PRV was issued upon approval of ZYCUBO by the U.S. Food and Drug Administration ("FDA") on January 12, 2026
- SECFortress Biotech Inc. filed SEC Form 8-K: Entry into a Material Definitive Agreement, Creation of a Direct Financial Obligation, Other Events, Financial Statements and Exhibits8-K - Fortress Biotech, Inc. (0001429260) (Filer)
- PRFortress Biotech's Subsidiary Cyprium Therapeutics Enters into Agreement to Sell Rare Pediatric Disease Priority Review Voucher for $205 MillionMIAMI, Feb. 23, 2026 (GLOBE NEWSWIRE) -- Fortress Biotech, Inc. (NASDAQ:FBIO) ("Fortress") and its majority-owned subsidiary, Cyprium Therapeutics, Inc. ("Cyprium"), today announced that Cyprium entered into a definitive asset purchase agreement to sell its Rare Pediatric Disease Priority Review Voucher ("PRV") for gross proceeds of $205 million upon the closing of the transaction. In December 2023, Sentynl Therapeutics, Inc. ("Sentynl") assumed full responsibility for the development and commercialization of ZYCUBO® (copper histidinate, formerly known as CUTX-101) from Cyprium. The PRV was issued upon approval of ZYCUBO by the U.S. Food and Drug Administration ("FDA") on January 12, 2026
- PRAvenue Therapeutics Enters into Exclusive Worldwide License Agreement for ATX-04 for the Treatment of Pompe DiseaseATX-04 is a selective β2-adrenergic agonist with human proof-of-concept data demonstrating improved muscle function and enhanced response to enzyme replacement therapy MIAMI, Feb. 23, 2026 (GLOBE NEWSWIRE) -- Avenue Therapeutics, Inc. (OTC:ATXI) ("Avenue" or the "Company"), a specialty pharmaceutical company focused on the development and commercialization of therapies for rare and neurologic diseases, today announced that it has entered into an exclusive worldwide license agreement with Duke University for patents and know-how pertaining to ATX-04 (clenbuterol), a well-characterized small-molecule β2-adrenergic agonist, in clinical development for the treatment of Pompe disease. Pompe d
- SECFortress Biotech Inc. filed SEC Form 8-K: Other Events, Financial Statements and Exhibits8-K - Fortress Biotech, Inc. (0001429260) (Filer)
- PRFortress Biotech and Cyprium Therapeutics Announce U.S. FDA Approval of ZYCUBO® (copper histidinate), the First and Only Approved Treatment for Menkes Disease in the United StatesRare Pediatric Disease Priority Review Voucher (PRV) granted by FDA at approval to be transferred from Sentynl Therapeutics to Cyprium Cyprium eligible to receive tiered royalties and up to $129 million in aggregate development and sales milestones from Sentynl Therapeutics MIAMI, Jan. 13, 2026 (GLOBE NEWSWIRE) -- Fortress Biotech, Inc. (NASDAQ:FBIO) ("Fortress") and its majority-owned subsidiary, Cyprium Therapeutics, Inc. ("Cyprium"), today announced that the U.S. Food and Drug Administration ("FDA") has approved ZYCUBO® (copper histidinate, formerly known as CUTX-101) for the treatment of Menkes disease in pediatric patients. In December 2023, Sentynl Therapeutics, Inc. ("Sentynl"),
- INSIDERDirector Klein Dov was granted 27,322 shares, increasing direct ownership by 27% to 130,105 units (SEC Form 4)4 - Fortress Biotech, Inc. (0001429260) (Issuer)
- INSIDERDirector Harvey Jimmie was granted 27,322 shares, increasing direct ownership by 23% to 146,704 units (SEC Form 4)4 - Fortress Biotech, Inc. (0001429260) (Issuer)
- INSIDERDirector Lorenz Kevin was granted 27,322 shares, increasing direct ownership by 37% to 101,009 units (SEC Form 4)4 - Fortress Biotech, Inc. (0001429260) (Issuer)
- INSIDERDirector Lobell J Jay was granted 27,322 shares, increasing direct ownership by 17% to 192,397 units (SEC Form 4)4 - Fortress Biotech, Inc. (0001429260) (Issuer)
- INSIDERDirector Hoenlein Malcolm was granted 27,322 shares, increasing direct ownership by 31% to 115,747 units (SEC Form 4)4 - Fortress Biotech, Inc. (0001429260) (Issuer)
- SECSEC Form 424B3 filed by Fortress Biotech Inc.424B3 - Fortress Biotech, Inc. (0001429260) (Filer)
- SECSEC Form EFFECT filed by Fortress Biotech Inc.EFFECT - Fortress Biotech, Inc. (0001429260) (Filer)