Iterion Therapeutics Expands Clinical Development of Tegavivint, a First-in-Class Wnt/β-Catenin Inhibitor, into Colorectal Cancer with First Patient Dosed

Tegavivint Targets the Central Oncogenic Driver in Colorectal Cancer as First-in-Class Clinical-Stage Wnt/β-Catenin Inhibitor

CRC Expansion Builds on Promising Monotherapy Activity and Favorable Safety Profile Observed in Advanced Hepatocellular Carcinoma

HOUSTON, March 25, 2026 /PRNewswire/ -- Iterion Therapeutics, a clinical-stage, biopharmaceutical company dedicated to advancing the treatment of Wnt-driven cancers, today reported that the first patient has been dosed at HonorHealth Research Institute in a phase 1/2 clinical trial (NCT07463599) evaluating tegavivint, a first-in-class, small molecule inhibitor of the Wnt/β-catenin pathway, for the treatment of metastatic colorectal cancer (mCRC). This milestone expands Iterion's clinical development into mCRC, a disease with significant unmet need and limited progress in developing targeted therapies.

"The mCRC study builds on the encouraging clinical benefit we're observing in patients with advanced hepatocellular carcinoma, including partial responses and durable disease control in heavily pre-treated patients," said Rahul Aras, PhD, President and CEO of Iterion Therapeutics. "The level of monotherapy activity observed with tegavivint in complex solid tumors is unprecedented for a Wnt/β-catenin pathway inhibitor and we're excited to expand development into other hard-to-treat Wnt-driven cancers."

Colorectal cancer is one of the most common cancers worldwide, with over 1.9 million new cases annually and a pressing need for novel therapies. After lung cancer, colorectal cancer is the second leading cause of cancer-related death in the U.S.

Despite advances in early detection, treatment options for advanced or metastatic CRC remain inadequate, highlighting the urgency for targeted approaches like tegavivint.

"While greater than 90% of colorectal cancer patients harbor Wnt-pathway activating mutations, there are no FDA-approved drugs targeting the pathway. This first patient dosed represents a critical step forward in addressing this therapeutic gap," said Sunil Sharma, MD, Chief of Translational Research and Drug Discovery at HonorHealth Research Institute. "Based on tegavivint's excellent tolerability profile and demonstrated clinical activity in other solid tumors, we're optimistic about its potential in colorectal cancer, including future combination strategies."

Tegavivint is a small-molecule inhibitor of TBL1, a transcriptional co-factor required for oncogenic β-catenin signaling. By selectively disrupting the TBL1/β-catenin transcriptional complex, tegavivint promotes degradation of nuclear β-catenin and suppresses β-catenin-dependent gene transcription, inhibiting Wnt-driven tumor growth while avoiding the dose-limiting toxicities historically associated with upstream Wnt inhibition.

Tegavivint has demonstrated favorable tolerability, pharmacodynamic activity, and encouraging monotherapy clinical responses in clinical trials in hepatocellular carcinoma and desmoid tumors, two diseases driven by aberrant Wnt/β-catenin signaling. These findings provide a robust foundation for expansion into mCRC, and underscore the drug's broad applicability across a substantial portion of newly diagnosed cancers worldwide in which aberrant Wnt/β-catenin signaling is a fundamental oncogenic driver.

About Iterion Therapeutics
Iterion Therapeutics is a clinical-stage oncology company developing first-in-class therapies that target cancers driven by aberrant Wnt/β-catenin signaling. The Company's lead asset, tegavivint, is the first and only small-molecule inhibitor of TBL1, a critical transcriptional regulator required for nuclear β-catenin stability and oncogenic gene expression. Tegavivint has demonstrated clinical tolerability, target engagement, and monotherapy activity in multiple complex solid tumors, including advanced hepatocellular carcinoma, positioning Iterion at the forefront of Wnt/β-catenin drug development.

Iterion is advancing a focused clinical strategy anchored by its lead program in hepatocellular carcinoma, with expansion into additional Wnt-driven cancers, including pediatric and rare oncology indications where Wnt/β-catenin signaling represents a validated disease driver. The Company has received $26 million in Product Development Awards from the Cancer Prevention and Research Institute of Texas (CPRIT) and continues to build a pipeline of differentiation-driven clinical opportunities around its proprietary Wnt/β-catenin platform. For more information on Iterion, please visit www.iteriontherapeutics.com.

Investor Contact:
Laurence Watts
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Media Contact:
Ryan Walker
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SOURCE Iterion Therapeutics