Clin2
NCT07032142Worth exploringNot yet recruiting

Study of an antidote for severe side effects from fluoropyrimidine chemotherapy

CancerToxicity Due to Chemotherapy

Part of Cancer clinical trials.

This study tests an experimental antidote to help people who have had severe side effects or an overdose from common chemotherapy drugs called fluoropyrimidines (like 5-FU or capecitabine). The goal is to find the best dose and see if it can reduce the severity of these side effects.

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

Phase
Phase 1/Phase 2
Enrollment
66 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You must be currently receiving a chemotherapy drug called a fluoropyrimidine (like 5-FU or capecitabine) for a solid tumor (not a blood cancer).
  • You must have had a severe side effect (grade 3 or 4) or an overdose from this drug, such as severe nausea, diarrhea, low blood counts, or mouth sores.
  • You must not be able to get the standard rescue medicine (uridine triacetate) for this toxicity.
  • You must be able to take medicines by mouth and be willing to avoid alcohol during the treatment period.
  • Your liver and kidney function must be within acceptable limits, and you must not have cirrhosis or severe kidney disease.
  • You must be willing to use highly effective birth control (if you or your partner can become pregnant) and avoid sperm donation for 6 months after the last dose.

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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