Welcome to our dedicated page for Fortress Biotech news (Ticker: FBIO), a resource for investors and traders seeking the latest updates and insights on Fortress Biotech stock.
Fortress Biotech, Inc. operates a biopharmaceutical business built around acquiring and advancing pharmaceutical and biotechnology assets. Company updates commonly cover product revenue, equity holdings, dividend and royalty income, FDA decisions, subsidiary transactions and clinical or regulatory progress across its portfolio.
Recurring news also includes Journey Medical dermatology products, Cyprium Therapeutics and ZYCUBO® for Menkes disease, priority review voucher monetization and corporate financial results. Fortress reports material developments involving approved prescription products, portfolio-company ownership, royalties, capital resources and business-development activity.
Fortress Biotech reported a 45.5% growth in net revenue for H1 2022, totaling $42.8 million. The company anticipates significant regulatory milestones, including a BLA submission for cosibelimab for metastatic cutaneous squamous cell carcinoma expected by year-end 2022. Journey Medical, a partner, achieved $18.3 million in Q2 2022, up 20% from Q2 2021. Fortress reported a net loss of $21.4 million for Q2 2022, contrasting with a $3.5 million loss in Q2 2021. Strong ongoing clinical trials and expanded product offerings position the company for future growth.
Fortress Biotech (NASDAQ: FBIO) announced that its subsidiary Helocyte received a grant from NIAID/NIH exceeding $20 million to fund a Phase 2 clinical trial for the Triplex CMV vaccine. This multi-center, randomized study will take place at up to 15 transplant centers across the U.S., focusing on liver transplant patients. The COLT trial aims to demonstrate Triplex's potential to enhance outcomes for these patients. Previous studies have shown Triplex to be safe and immunogenic, with over 100 subjects dosed.
Journey Medical reported a 20% increase in net revenue for Q2 2022, totaling $18.3 million, compared to $15.3 million in Q2 2021. This growth was supported by settlement agreements with Padagis ensuring exclusivity for key products. Enrollment in the DFD-29 Phase 3 trials is progressing, with top-line data expected in early 2023 and an NDA filing anticipated in the second half of 2023. Despite a $7.5 million net loss, there was an improved Non-GAAP Adjusted EBITDA loss of $(2.6) million. The company’s cash reserves are at $38.1 million.
Journey Medical Corporation (NASDAQ: DERM) will release its Q2 2022 financial results on August 9, 2022, after market close. A conference call will follow at 4:30 p.m. ET, allowing investors to discuss the results and receive a corporate update. Interested participants can dial in 10 minutes early and join the call. A live audio webcast will also be available on their website, with a replay option for 30 days. Journey Medical focuses on developing and commercializing dermatology products, with nine marketed treatments currently.
Fortress Biotech, Inc. (NASDAQ: FBIO) has appointed David Jin as Chief Financial Officer effective August 16, 2022, while Robyn Hunter will step down after 11 years to pursue other opportunities. Chairman Lindsay A. Rosenwald expressed confidence in Jin's capabilities, highlighting his contributions to the company and its strategy. Jin noted Fortress's ongoing projects, including FDA submissions and collaborations, while emphasizing the company's commitment to innovation in biopharmaceuticals. The transition aims to maintain stability and growth during this critical period.
Fortress Biotech (FBIO) announced that its subsidiary UR-1 Therapeutics has dosed the first patient in a Phase 1 clinical trial of Dotinurad, a URAT1 inhibitor for gout in the U.S. This trial aims to assess safety, tolerability, pharmacokinetics, and pharmacodynamics of Dotinurad, building on its previous success in Japan where it showed efficacy in over 500 patients. Fortress expects topline data release in the second half of 2022 and aims to establish Dotinurad as a leading oral therapy for serum uric acid reduction, potentially reaching millions in the U.S.
Journey Medical (NASDAQ: DERM) announced a settlement with Padagis US LLC regarding patents for three key products: QBREXZA, AMZEEQ, and ZILXI. Under the agreement, Padagis cannot launch generics until August 15, 2030, July 1, 2031, and April 1, 2027, respectively. This settlement is aimed at solidifying Journey Medical's market exclusivity and supporting sales growth for these dermatological products. The CEO emphasized the importance of enforcing intellectual property rights to benefit the company, shareholders, and patients relying on these treatments.
Journey Medical Corporation (NASDAQ: DERM), a pharmaceutical company specializing in dermatology, will present at the B. Riley Securities 22nd Annual Institutional Investor Conference on May 26, 2022. CEO Claude Maraoui will provide a corporate overview at 12:20 p.m. PT and will engage in one-on-one meetings during the event. Journey Medical focuses on innovative dermatology products and currently markets nine such products. Founded by Fortress Biotech (NASDAQ: FBIO), the company is headquartered in Scottsdale, Arizona.
Fortress Biotech (NASDAQ: FBIO) announced that its Chairman and CEO, Lindsay A. Rosenwald, M.D., will participate in two investor conferences in May 2022. The events include the H.C. Wainwright Global Investment Conference on May 24, 2022, at 9:30 a.m. ET, and the B. Riley Securities 22nd Annual Institutional Investor Conference on May 26, 2022, at 10:10 a.m. PT. A webcast of the H.C. Wainwright presentation will be available on Fortress' website for 30 days. Fortress focuses on acquiring and developing high-potential therapeutic products across various medical fields.
Fortress Biotech (FBIO) reported a remarkable 106% increase in net revenue for Q1 2022, reaching $23.9 million compared to $11.6 million in Q1 2021. The company ended the quarter with $289.7 million in cash and cash equivalents. Positive results from the clinical trial of cosibelimab for metastatic cSCC were noted, with a BLA submission expected in 2022. Additionally, the rolling NDA for CUTX-101 for Menkes disease is targeted for completion in mid-2022. Significant patient data and multiple regulatory submissions are anticipated throughout the year.