Fortress Biotech, Inc., together with its subsidiaries, operates as a biopharmaceutical company in the United States and internationally. The company offers Emrosi, a minocycline hydrochloride extended-release capsule for the treatment of rosacea; Qbrexza a medicated cloth towelette for the treatment of axillary hyperhidrosis; Accutane, an oral isotretinoin drug for the treatment of severe recalcitrant nodular acne; Amzeeq, a minocycline topical foam for the treatment of lesions of non-nodular moderate to severe acne vulgaris; Zilxi, a minocycline topical foam for the treatment of lesions of rosacea; Exelderm, an antifungal cream for topical use; Targadox, an oral doxycycline drug for the therapy of severe acne; Luxamend, a water-based emulsion for the treatment of superficial wounds, minor cuts or scrapes, dermal ulcers, donor sites, first and second-degree burns, and radiation dermatitis; and UNLOXCYT, a death-ligand 1 blocking antibody for the treatment of metastatic cutaneous squamous cell carcinoma. It also develops CUTX-101, a copper histidinate injection, which is in FDA approved stage for the treatment of Menkes disease; IV Tramadol, an intravenous formulation, which is in NDA/BLA filed stage for the treatment of post-operative acute pain; Dotinurad, a urate transporter inhibitor, which is in Phase III for the treatment of gout and chronic kidney diseases; CAEL-101, a light chain fibril-reactive monoclonal antibody, which is in Phase III for the treatment of amyloid light chain amyloidosis; and Triplex, a universal recombinant modified vaccinia ankara viral vector vaccine, which is in Phase II for the treatment of cytomegalovirus, anti-human immunodeficiency virus, non-hodgkin lymphoma, and acute lymphoblastic leukemia. The company was formerly known as Coronado Biosciences, Inc. and changed its name to Fortress Biotech, Inc. in April 2015. Fortress Biotech, Inc. was incorporated in 2006 and is based in Bay Harbor Islands, Florida. Show more
1111 Kane Concourse, Bay Harbor Islands, FL, 33154, United States
Market Cap
84.04M
52 Wk Range
$1.67 - $4.53
Previous Close
$2.53
Open
$2.57
Volume
87,489
Day Range
$2.56 - $2.68
Enterprise Value
-118.2M
Cash
255.8M
Avg Qtr Burn
N/A
Insider Ownership
22.79%
Institutional Own.
18.16%
Qtr Updated
03/31/26
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| Drug & Indication | Stage & Event | Catalyst Date |
|---|---|---|
Emrosi/Minocycline (DFD-29) (Tetracycline Antibiotic) Details Inflammatory Lesions Of Rosacea In Adults | Approved Quarterly sales | |
UNLOXCYT/Cosibelimab-Ipdl (PD-1 Inhibitor) Details Metastatic Or Locally Advanced Cutaneous Squamous Cell Carcinoma | Approved Quarterly sales | |
ZYCUBO® (copper histidinate) Details Menkes Disease | Approved Quarterly sales | |
Dotinurad Details Chronic refractory gout | Phase 3 Data readout | |
Anselamimab (CAEL-101) Details Amyloid light chain amyloidosis (Mayo Stage IIIa & Mayo Stage IIIb) | Phase 3 Update | |
Triplex Details Co-infected w/ Cytomegalovirus (CMV) and Human immunodeficiency virus (HIV) | Phase 2 Data readout | |
Triplex Details Cytomegalovirus (CMV) | Phase 2 Data readout | |
Triplex Details Cytomegalovirus (CMV) | Phase 2 Data readout | |
Clenbuterol (ATX-04) (Beta-2 Agonist) Details Pompe Disease | Phase 2 Update | |
Triplex Details Cytomegalovirus (CMV) control in pediatric patients | Phase 1/2 Data readout | |
Triplex + Allogeneic CMV-Specific CD19-CAR T Cells Details Acute lymphoblastic leukemia | Phase 1 Data readout | |
Triplex + bi-specific CMV/CD19 CAR T cell therapy Details Non-Hodgkin lymphoma | Phase 1 Data readout | |
Triplex + CMV-Specific CD19-CAR T-cells Details Non-Hodgkin lymphoma | Phase 1 Data readout | |
CEVA-101 Details Traumatic brain injury | Failed Discontinued |
