Harpoon Therapeutics Presents Data for New ProTriTAC™ Development Candidates in TROP2- and ITGB6-expressing Solid Tumors at AACR 2023
“TROP2 and ITGB6 are tumor targets that are overexpressed in numerous solid tumor types and have demonstrated clinical utility when targeted as antibody drug conjugates,” said
“Our ProTriTAC platform is designed to improve the therapeutic index of T cell engagers targeting solid tumor antigens,” said
Highlights from the posters include:
Abstract #2927: ITGB6 ProTriTAC™, a protease-activated T cell engager prodrug targeting Integrin-β6 for the treatment of solid tumors
ITGB6 protein is expressed in multiple tumor types, including cervical, lung, and head and neck, among others. In rodent established tumor models, ITGB6 ProTriTAC showed efficient prodrug activation and potent anti-tumor activity in vivo with complete tumor eradication at doses as low as 30 µg/kg. In cynomolgus monkeys, ITGB6 ProTriTAC showed favorable pharmacokinetic and safety profiles and was well-tolerated up to 540 µg/kg, the highest dose tested. Hematological changes consisted of minimally to moderately decreased neutrophils at all dose levels, as well as transient decreases in lymphocytes and basophils in week three of the study. There were no notable findings in plasma cytokines (IFNγ, IL-1β, IL-2, IL-6, IL-10, IL-8, TNF-α), coagulation, clinical chemistry, or urinalysis parameters. Additionally, there were no notable histopathological findings based on organ weight, gross and microscopic examination.
Abstract #2928: TROP2 ProTriTAC™, a protease-activated T cell engager prodrug targeting TROP2 for the treatment of solid tumors
TROP2 protein is expressed in multiple solid tumor types, including cervical, prostate and ovarian, among others. In rodent established tumor models, TROP2 ProTriTAC had highly potent anti-tumor activity in vivo with complete tumor eradication at doses as low as 30 µg/kg. In cynomolgus monkeys, TROP2 ProTriTAC showed favorable pharmacokinetics and was well-tolerated up to 180 µg/kg, whereas 540 µg/kg triggered on-target toxicity with mixed cell infiltrates in organs where normal tissue expression of TROP2 is expected. There were no notable findings in serum cytokines (IFNγ, IL-1β, IL-2, IL-6, IL-10, IL-8, TNF-α) throughout the study.
For more details about the AACR Annual Meeting, please visit:
The posters will be available on Harpoon’s website following today’s presentations.
Harpoon’s three distinct T cell engager platforms are designed to potentially allow more patients to get maximum clinical benefit while maintaining the best possible quality of life. Harpoon’s first platform, the constitutively active TriTAC® (Tri-specific T cell activating construct), is designed to minimize off-target toxicities, and is ideal for targets with limited on-target liabilities. The ProTriTAC platform offers similar advantages and adds an element of spatial control, with activation directed primarily to the tumor microenvironment. This spatial control of activation may address on-target tissue damage, hence enabling an expansion of the T cell engager target space. The TriTAC-XR™ platform (extended-release with slow activation in circulation) adds improved temporal control and is designed to be activated in the systemic circulation at a predefined rate to minimize on-target cytokine release syndrome (CRS).
Harpoon Therapeutics is a clinical-stage immuno-oncology company developing a novel class of T cell engagers that harness the power of the body’s immune system to treat patients suffering from cancer and other diseases. T cell engagers are engineered proteins that direct a patient’s own T cells to kill target cells that express specific proteins, or antigens, carried by the target cells. Using its proprietary Tri-specific T cell Activating Construct (TriTAC®) platform, Harpoon is developing a pipeline of novel TriTACs initially focused on the treatment of solid tumors and hematologic malignancies. Harpoon has also developed a proprietary ProTriTAC™ platform, which applies a prodrug concept to its TriTAC platform to create a therapeutic T cell engager that remains inactive until it reaches the tumor. Harpoon’s third proprietary technology platform, extended release TriTAC-XR, is designed to mitigate cytokine release syndrome. For additional information about
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Words such as “may,” “expect,” “potential,” “further,” “will,” and similar expressions (as well as other words or expressions referencing future events, conditions or circumstances) are intended to identify forward-looking statements. These forward-looking statements are based on Harpoon Therapeutics’ expectations and assumptions as of the date of this press release. Each of these forward-looking statements involves risks and uncertainties that could cause Harpoon Therapeutics’ clinical development programs, future results or performance to differ significantly from those expressed or implied by the forward-looking statements. Forward-looking statements contained in this press release include, but are not limited to, statements about the expected progress, results, and plans pertaining to Harpoon Therapeutics’ clinical trials, the association of interim clinical data and preclinical results with potential treatment outcomes, and other statements that are not historical fact. Many factors may cause differences between current expectations and actual results, including unexpected safety or efficacy data observed during clinical studies, preliminary data and trends may not be predictive of future data or results, may not demonstrate safety or efficacy or lead to regulatory approval by the FDA or other regulatory agencies, clinical trial site activation or enrollment rates that are lower than expected, changes in expected or existing competition, changes in the regulatory environment, the uncertainties and timing of the regulatory approval process, the timing and results of unexpected litigation or other disputes, and the sufficiency of Harpoon Therapeutics’ cash resources. These and other factors that may cause Harpoon Therapeutics’ actual results to differ from those expressed or implied in the forward-looking statements in this press release are discussed in Harpoon Therapeutics’ filings with the U.S. Securities and Exchange Commission, including under “Risk Factors” in Harpoon Therapeutics’ annual report on Form 10-K for the year ended
Source: Harpoon Therapeutics