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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 $9.0 million to date with an estimated additional $12 million over the next four years in support of the Phase 2 clinical trial. The trial will be conducted in up to 20 nationally recognized transplant centers in the United States. Triplex was initially developed by City of Hope, a world-renowned cancer treatment and research organization, and exclusively licensed to Helocyte.
Posted In: FBIO
