OncoMatch/Clinical Trials/NCT04851119
Tegavivint for the Treatment of Recurrent or Refractory Solid Tumors, Including Lymphomas and Desmoid Tumors
Is NCT04851119 recruiting? Yes, currently enrolling (May 2026). This Phase 1/2 trial studies Tegavivint for colorectal carcinoma.
Treatment: Tegavivint — This phase I/II trial evaluates the highest safe dose, side effects, and possible benefits of tegavivint in treating patients with solid tumors that has come back (recurrent) or does not respond to treatment (refractory). Tegavivint interferes with the binding of beta-catenin to TBL1, which may help stop the growth of tumor cells by blocking the signals passed from one molecule to another inside a cell that tell a cell to grow.
Check if I qualifyExtracted eligibility criteria
Cancer type
Colorectal Cancer
Endometrial Cancer
Melanoma
Neuroblastoma
Ovarian Cancer
Pancreatic Cancer
Sarcoma
Hepatocellular Carcinoma
Tumor Agnostic
Non-Hodgkin Lymphoma
Osteosarcoma
Biomarker criteria
Required: CTNNB1 S37F, S45F, T41A, S45P, S33C, S37C, D32Y, S33F, T41I, G34R, G34V, D32N, S33P, G34E, D32G
the most common CTNNB1 mutations (S37F, S45F, T41A, S45P, S33C, S37C, D32Y, S33F, T41I, G34R, G34V, D32N, S33P, G34E, D32G)
Required: APC loss of function
any loss of function mutations in the APC
Required: AXIN2 loss of function
any loss of function mutations in the ... Axin2FBXW7
Required: FBXW7 loss of function
any loss of function mutations in the ... Axin2FBXW7
Required: TCF7L2 loss of function
any loss of function mutations in the ... TCF7L2
Required: RNF43 loss of function
any loss of function mutations in the ... RNF43
Required: GSK3B gain of function
any gain-of-function mutations in the GSK3B
Required: LRP6 gain of function
any gain-of-function mutations in the ... LRP6
Required: LGR5 gain of function
any gain-of-function mutations in the ... LGR5
Required: CTNNB1 nuclear beta-catenin (strong nuclear staining)
IHC showing strong nuclear beta-catenin staining
Performance status
ECOG/KARNOFSKY/LANSKY 0–2
ECOG scores of 0, 1 or 2. Use Karnofsky for patients > 16 years of age and Lansky for patients <= 16 years of age
Prior therapy
Cannot have received: tegavivint
Lab requirements
Blood counts
ANC >= 1000/uL; Platelets >= 100,000/uL (transfusion independent); Hemoglobin >= 8.0 g/dL
Kidney function
Creatinine clearance or GFR >= 70 mL/min/1.73 m^2 or age/gender-based creatinine
Liver function
Bilirubin <= 1.5 x ULN for age; ALT (SGPT) <= 135 U/L (ULN=45 U/L); Albumin >= 2 g/dL
See inclusion criteria for detailed thresholds
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- Children's Hospital of Alabama · Birmingham, Alabama
- Children's Hospital Los Angeles · Los Angeles, California
- Children's Hospital of Orange County · Orange, California
- Lucile Packard Children's Hospital Stanford University · Palo Alto, California
- UCSF Medical Center-Mission Bay · San Francisco, California
Showing up to 5 US sites. See all sites on ClinicalTrials.gov →
Could you qualify for this trial?
Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.
Check if I qualify