News
FBIO
3.540
+6.63%
0.220
Weekly Buzz: CYTK Scores First FDA Approval, INSM Ends Rhinosinusitis Study, XOMA Acquires GBIO
NASDAQ · 1d ago
Fortress Biotech Amends Credit Agreement with Oaktree
TipRanks · 5d ago
Fortress Biotech Announces Unregistered Sale of Warrants in Private Placement
Reuters · 5d ago
Optimistic Buy Rating for Fortress Biotech Driven by Promising CUTX-101 Prospects and FDA Engagement
TipRanks · 5d ago
Fortress Biotech Rises After FDA Accepts Application for Menkes Treatment
Dow Jones · 5d ago
Fortress Biotech’s CUTX-101 NDA Resubmission Accepted by FDA
TipRanks · 5d ago
Cyprium Therapeutics Gains FDA Acceptance for CUTX-101 NDA Resubmission
Reuters · 5d ago
FDA Accepts Fortress Biotech and Cyprium Therapeutics CUTX-101 NDA Resubmission
Reuters · 5d ago
FORTRESS BIOTECH INC - PDUFA TARGET DATE FOR CUTX-101 SET FOR JANUARY 14, 2026
Reuters · 5d ago
Weekly Report: what happened at FBIO last week (1208-1212)?
Weekly Report · 6d ago
JOURNEY MEDICAL CORPORATION ANNOUNCES PUBLICATION OF CLINICAL TRIAL RESULTS ASSESSING THE IMPACT OF EMROSI™ (DFD-29) ON MICROBIAL FLORA OF HEALTHY ADULTS IN THE JOURNAL OF DRUGS IN DERMATOLOGY
Reuters · 12/10 13:30
Weekly Report: what happened at FBIO last week (1201-1205)?
Weekly Report · 12/08 10:10
Avenue Therapeutics Inc. Announces Date for Upcoming Annual Stockholder Meeting
Reuters · 12/05 21:02
Mustang Bio Inc. Announces Date for Upcoming Annual Stockholder Meeting
Reuters · 12/03 21:06
Weekly Report: what happened at FBIO last week (1124-1128)?
Weekly Report · 12/01 10:06
Weekly Report: what happened at FBIO last week (1117-1121)?
Weekly Report · 11/24 10:10
Fortress Biotech’s Subsidiary Resubmits NDA for CUTX-101
TipRanks · 11/17 13:00
Sentynl Resubmits CUTX-101 NDA to FDA for Menkes Disease Treatment
Reuters · 11/17 12:33
FORTRESS BIOTECH INC: ON NOV 14, SENTYNL NOTIFIED CYPRIUM THAT SENTYNL HAD RESUBMITTED THE NDA FOR CUTX-101 TO THE FDA
Reuters · 11/17 12:32
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About FBIO
Fortress Biotech, Inc. is a biopharmaceutical company focused on acquiring and advancing assets. The Company has eight marketed prescription pharmaceutical products and over 20 programs in development, with its majority-owned and majority-controlled partners and subsidiaries and partners and subsidiaries it founded and in which it holds significant minority ownership positions. Its portfolio is being commercialized and developed for various therapeutic areas, including oncology, dermatology, and rare diseases. Its dermatology products include Emrosi, Qbrexza, Amzeeq, Zilxi, Exelderm, Targadox, and Luxamend. Its late-stage product candidates include CUTX-101 (copper histidinate injection for Menkes disease), Triplex (cytomegalovirus (CMV) vaccine), and CAEL-101 (monoclonal antibody for AL amyloidosis). Its early and mid-stage product candidates include Dotinurad (urate transporter (URAT1) inhibitor for gout), MB-101 (IL13Rα2 CAR T Cell Program for Glioblastoma), and others.