Clin2
NCT04851119Possibly a fitRecruiting

Tegavivint for kids and young adults with hard-to-treat solid tumors

Colorectal CarcinomaEndometrial CarcinomaMelanomaNeuroblastomaOvarian CarcinomaPancreatic Ductal AdenocarcinomaRecurrent Desmoid FibromatosisRecurrent Ewing Sarcoma

Treatments studied

Part of Blood & lymphatic, Cancer, Digestive system, Genetic & congenital, Hormones & metabolism, Immune system & allergy, Kidney & urinary, Skin, Women’s health & pregnancy clinical trials.

This early-phase study tests tegavivint to see how well it works and how safe it is for children and young adults with solid cancers that have come back or are not responding. It may be an option if your tumor type (including certain lymphomas or desmoid tumors) matches the study’s rules.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 1/Phase 2
Enrollment
147 people
Ages
1 year to 30 years
Study type
Interventional

Who can take part

  • You’re age 1 month to 21 years old for the main group, or up to 30 years old for specific tumor groups
  • Your cancer is a solid tumor that has returned or is resistant to treatment (includes certain lymphomas and desmoid tumors)
  • Your cancer was confirmed by a tissue biopsy, and you have measurable disease (desmoid must be judged not safe to remove)
  • You must be well enough to do daily activities: performance score must be 0, 1, or 2 (based on age-appropriate scales)
  • You must have recovered from prior cancer treatment, with a required waiting time and no prior tegavivint exposure
  • Blood and organ tests must be within required ranges (including bone marrow functioning depending on whether it’s involved)

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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