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Achieved complete target inhibition, durable tumor control, and a 36-fold dose range without dose-limiting toxicity— advancing toward combination trials.
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TRE-515, the only dCK inhibitor in development, secures $1.8M NIH grant after outperforming market-leader Stelara in Crohn’s studies.
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Phase 1 enrollment of TRE-515 in solid tumors completed; 36-fold dose escalation well tolerated, with early signs of antitumor activity and durable benefit
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Fresh NIH funding follows FDA Fast Track designation, reinforcing confidence in TRE-515 potential to advance prostate cancer treatment.
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$3M NIH grant advances TRE-515, a first-in-class lupus therapy. Funding supports safety, biomarker studies, and paves the way for patient trials.
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Creates platform for precision dosing, companion diagnostics, streamlined development, and broader use across cancer and autoimmune diseases.
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TRE-515 receives FDA Fast Track for use with Pluvicto™ in advanced prostate cancer, aiming to improve outcomes in PSMA-positive, treatment-resistant cases.
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Global exclusive agreement expands patent coverage for compound structures and autoimmune uses across major pharmaceutical markets
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Trethera enlists leading expert in demyelinating diseases to advance TRE-515, a first-in-class drug with FDA Orphan Drug status for ADEM and optic neuritis
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LOS ANGELES, April 22, 2025 (GLOBE NEWSWIRE) -- Trethera Corporation (“Trethera”), a clinical stage biopharmaceutical company developing first-in-class therapies for cancer and autoimmune diseases,...