Fortress Biotech Announces First Patient Dosed in Multi-Center Phase 2 Study of Triplex for Control of CMV in Patients Undergoing Liver Transplantation
Fortress Biotech, in collaboration with its subsidiary Helocyte, announced the commencement of a Phase 2 clinical trial for Triplex, a vaccine targeting cytomegalovirus (CMV) in liver transplant patients. The trial is funded by a $9 million grant from the NIH/NIAID, with an additional $12 million expected over the next four years. Conducted at up to 20 U.S. transplant centers, this randomized, placebo-controlled study will involve 416 participants. The primary objective is to assess Triplex's efficacy in reducing CMV antiviral therapy duration within the first 100 days post-transplant. Secondary endpoints include the development and onset timing of CMV disease within six months post-transplant. This trial aims to address the significant unmet need for effective CMV therapies in transplant settings.
- First patient dosed in Phase 2 clinical trial, marking a significant milestone.
- NIH/NIAID funding: $9 million received, with an additional $12 million expected.
- Trial to be conducted in up to 20 nationally recognized U.S. transplant centers.
- Primary objective: Assessing reduced CMV antiviral therapy duration within 100 days post-transplant.
- Study involves 416 participants, enhancing the robustness of the data.
- Triplex licensed from City of Hope, a notable cancer treatment and research organization.
- Potential to address significant unmet medical need in CMV management for transplant patients.
- Uncertainty remains regarding the ultimate efficacy and safety of Triplex until trial completion.
- Significant financial investment without guaranteed successful outcomes.
- Potential risk of adverse side effects or lack of efficacy in participants.
- Extended trial duration may delay potential market availability of Triplex.
- Dependence on continued NIH/NIAID funding for trial progression.
Insights
The initiation of a Phase 2 clinical trial for Triplex, a vaccine designed to control cytomegalovirus (CMV) in liver transplant patients, is a significant milestone. CMV is a persistent issue in organ transplants, leading to severe complications and impacting patient survival rates. The trial's randomized, placebo-controlled and double-blinded design across multiple centers adds robustness to the findings, increasing the credibility and potential impact of the study results.
Triplex's development and subsequent trials are crucial, given the limited options currently available to manage CMV in transplant patients. If the trial proves successful, Triplex could become a standard prophylactic treatment, reducing the need for antiviral therapies, which often come with their own sets of complications and side effects. This would not only improve the quality of life for transplant recipients but also reduce healthcare costs associated with managing CMV-related complications.
The $9 million funding from NIH/NIAID, with an additional estimated $12 million over the next four years, is a strong endorsement of the potential of Triplex. This financial backing provides substantial support for the trial, reducing the financial burden on Fortress Biotech and allowing them to focus resources on other promising projects as well. This diversified funding stream underscores the confidence that significant institutions have in the potential success of Triplex.
Furthermore, if Triplex proves effective, the financial implications for Fortress Biotech are substantial. Achieving success in this trial could lead to commercialization, opening up new revenue streams. Given the high unmet medical need, Triplex could command a significant market share in the transplant sector. Investors should watch for interim results from this trial, as they could serve as early indicators of the potential market acceptance and financial success of Triplex.
Helocyte, a majority-owned subsidiary of Fortress Biotech, is developing Triplex for the prevention and treatment of cytomegalovirus in multiple transplant indications, as well as HIV
Clinical trial funded by a NIAID grant to a multi-center university consortium
Study is evaluating whether Triplex is safe and effective in improving the outcomes of liver transplant recipients
MIAMI, May 14, 2024 (GLOBE NEWSWIRE) -- Fortress Biotech, Inc. (Nasdaq: FBIO) (“Fortress”), an innovative biopharmaceutical company focused on acquiring and advancing assets to enhance long-term value for shareholders through product revenue, equity holdings and dividend and royalty revenue, and its majority-owned subsidiary, Helocyte, Inc. (“Helocyte”), today announced that the first patient was dosed in a multi-center, placebo-controlled, randomized Phase 2 study of Triplex, a vaccine for control of cytomegalovirus (“CMV”), in patients undergoing liver transplantation. The trial is funded by a grant from the National Institutes of Health’s National Institute of Allergy and Infectious Diseases (“NIH/NIAID”) to University of Washington Seattle. This grant has provided
Ajit Limaye, M.D., Professor of Medicine and Director of the Solid Organ Transplant Infectious Disease Program at the University of Washington and Principal Investigator of the “CMV vaccine in Orthotopic Liver Transplant” (“COLT”, see NCT06075745) trial, said, “The first dosing in this multi-center Phase 2 clinical trial is a major milestone and the culmination of years of effort to advance Triplex. There remains a significant unmet medical need to develop new therapies that can reduce the frequency and severity of CMV events in the organ transplant setting, where CMV continues to present life-threatening complications that directly impact patient outcomes and survival.”
COLT is a multi-center, randomized, placebo-controlled, double-blinded clinical trial in up to 416 CMV seronegative prospective liver transplant recipients to determine the safety and efficacy of two doses of Triplex, a Modified Vaccinia Ankara-vectored CMV vaccine, administered to participants anticipated to receive transplant within one to twelve months after study enrollment. The primary objective of the trial is to assess the effect of pre-transplant Triplex vaccination on the duration of CMV antiviral therapy within the first 100 days post-transplant in CMV seronegative liver transplant recipients whose liver donor is CMV seropositive. Secondary endpoints relate to the development of CMV disease by six months post-transplant as well as time to onset.
Lindsay A. Rosenwald, M.D., Chairman, President, and Chief Executive Officer of Fortress, said, “We are very pleased with the advancement of Triplex in this Phase 2 clinical trial evaluating CMV control in liver transplantation. If successful, this trial could demonstrate the potential of Triplex to significantly improve the outcomes, morbidity, and mortality of liver transplant recipients. Our Triplex vaccine is currently the subject of multiple ongoing and planned clinical trials for the prevention and treatment of CMV in several transplant indications, as well as in HIV. We look forward to providing updates as these trials progress.”
About Triplex
Triplex is a universal (non-HLA-restricted) recombinant Modified Vaccinia Ankara viral vector vaccine engineered to induce a robust and durable virus-specific T cell response to three immuno-dominant proteins [UL83 (pp65), UL123 (IE1), UL122 (IE2)] linked to CMV complications in the post-transplant setting. In completed Phase 1 (see NCT01941056) and Phase 2 (see NCT02506933, NCT03383055) studies, Triplex was found to be safe, well-tolerated and highly immunogenic. Triplex is currently the subject of multiple ongoing clinical trials, including: a Phase 2 evaluation for CMV control in recipients of liver transplant (see NCT06075745); a Phase 1/2 trial for CMV control in pediatric recipients of HCT (see NCT03354728); a Phase 2 trial for safety and immunogenicity in adults living with HIV and CMV (see NCT05099965); a Phase 2 trial for CMV control in recipients of stem cell transplant in which the stem cell donor is vaccinated with Triplex (see NCT06059391) and a Phase 1 trial of Triplex in combination with a bi-specific CMV/CD19 Chimeric Antigen Receptor (CAR) T cell for the treatment of non-Hodgkin lymphoma (see NCT05432635). Triplex is also the subject of several planned studies, including a Phase 2 trial for CMV control in recipients of kidney transplant. In 2023, Helocyte additionally entered into an option agreement with City of Hope for exclusive worldwide rights to a novel bispecific CMV/HIV CAR T cell therapy (optionally for use in combination with Triplex), which is currently the subject of a Phase 1 trial in adults living with HIV-1 (see NCT06252402).
About Helocyte
Helocyte is a clinical-stage company developing novel immunotherapies for the prevention and treatment of cancer and infectious diseases, including cytomegalovirus (“CMV”) and human immunodeficiency virus (“HIV”). The Centers for Disease Control estimate that 50 to 80 percent of Americans are living with CMV by the age of 40. While the virus is asymptomatic in healthy individuals, it can cause severe and life-threatening disease in those with weakened or uneducated immune systems. Patients undergoing allogeneic stem cell and solid organ transplantation are at particularly high risk of experiencing complications associated with CMV. According to the Center for International Blood and Marrow Transplant Research, there were over 9,300 allogeneic (unrelated and related) bone marrow and cord blood transplants performed in the United States in 2021. According to preliminary data from the Organ Procurement and Transplantation Network, there were over 46,000 organ transplants performed in the United States in 2023, comprised primarily of kidney and liver transplant procedures. Helocyte’s Triplex vaccine is engineered to induce a robust and durable virus-specific T cell response to control CMV in transplant recipients. While current antiviral therapies have reduced the rate of CMV disease-related mortality in transplant recipients, such treatments have been linked to increased toxicity, delayed immune reconstitution and late onset of CMV. The Helocyte vaccines may also educate the body’s innate immune system to fight CMV. For more information, please visit www.helocyte.com.
About Fortress Biotech
Fortress Biotech, Inc. (“Fortress”) is an innovative biopharmaceutical company focused on acquiring and advancing assets to enhance long-term value for shareholders through product revenue, equity holdings and dividend and royalty revenue. The company has seven marketed prescription pharmaceutical products and over 20 programs in development at Fortress, at its majority-owned and majority-controlled partners and subsidiaries and at partners and subsidiaries it founded and in which it holds significant minority ownership positions. Such product candidates span six large-market areas, including oncology, rare diseases and gene therapy, which allow it to create value for shareholders. Fortress advances its diversified pipeline through a streamlined operating structure that fosters efficient drug development. The Fortress model is focused on leveraging its significant biopharmaceutical industry expertise and network to further expand the company’s portfolio of product opportunities. Fortress has established partnerships with some of the world’s leading academic research institutions and biopharmaceutical companies to maximize each opportunity to its full potential, including AstraZeneca, City of Hope, Fred Hutchinson Cancer Center, Nationwide Children’s Hospital and Sentynl. For more information, visit www.fortressbiotech.com.
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Company Contact:
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Fortress Biotech, Inc.
(781) 652-4500
ir@fortressbiotech.com
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