Fortress Biotech Q1 EPS $2.82 Beats $(0.22) Estimate, Sales $16.038M Miss $16.338M Estimate
Journey Medical Corporation Secures Contract with Third Major GPO for Emrosi™
Fortress Biotech Reports 2025 Financial Results and Recent Corporate Highlights
Fortress Biotech Q4 EPS $(0.30) Beats $(0.42) Estimate, Sales $16.079M Miss $21.018M Estimate
Fortress Biotech’s Subsidiary Cyprium Therapeutics Closes Sale of Rare Pediatric Disease Priority Review Voucher for $205 Million
Fortress Biotech And Cyprium Therapeutics Announce The Closing Of The Sale Of Cyprium's Rare Pediatric Disease Priority Review Voucher For Gross Proceeds Of $205M
Journey Medical Corporation Reports Full-Year 2025 Financial Results and Recent Corporate Highlights
Journey Medical Corporation to Announce Year End 2025 Financial Results on March 25, 2026
Fortress Biotech’s Cyprium enters agreement to sell PRV for $205M
UPDATE: Fortress Biotech’s Subsidiary Cyprium Therapeutics Enters into Agreement to Sell Rare Pediatric Disease Priority Review Voucher for $205 Million
Fortress Biotech’s Subsidiary Cyprium Therapeutics Enters into Agreement to Sell Rare Pediatric Disease Priority Review Voucher for $205 Million
HC Wainwright & Co. Reiterates Buy on Fortress Biotech, Maintains $17 Price Target
Fortress Biotech Subsidiary Cyprium Therapeutics To Sell Rare Pediatric Disease Priority Review Voucher For $205M
Fortress Biotech: The PRV Catalyst That Could Reprice This Microcap
Fortress Biotech, Inc. (NASDAQ:FBIO) Could Be Less Than A Year Away From Profitability
Fortress 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 States
Fortress Biotech Announces FDA Approves Its ZYCUBO To Treat Menkes Disease In Pediatric Patients
Fortress Biotech shares are trading higher after the company and its subsidiary, Cyprium Therapeutics, announced that the FDA has accepted the resubmission of the NDA for CUTX-101, intended to treat Menkes disease in pediatric patients.
Fortress Biotech and Cyprium Therapeutics Announce FDA Acceptance of CUTX-101 NDA Resubmission
Fortress Biotech And Cyprium Therapeutics Announce FDA Acceptance Of Resubmission Of CUTX-101 NDA
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