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A Study of REC-4881 in Participants With Cancers Which Have an AXIN1 or APC Mutation

Join a trial studying REC-4881 for specific cancer mutations.

Recruiting
55 years and older
All
Phase 2

This study looks at how safe and effective a new drug called REC-4881 is for patients with certain types of cancer. The drug is for people with a specific gene change, called a mutation, in either AXIN1 or APC. These are genes that help control cell growth. The study is open-label, meaning both doctors and patients know they are getting the drug. Participants will take 12 mg of the drug by mouth every day for up to two years. The study will involve about 60 people, split into two groups based on their gene mutation. To join, you must be 55 or older, have a certain type of tumor that can't be removed by surgery, and have tried other cancer treatments without success. You cannot join if you've recently taken a similar drug or have a low heart function.

  • This study lasts up to 2 years, with daily medication.
  • Participants must have specific gene changes in their cancer.
  • Some past treatments and heart issues may exclude participation.
Study details
    AXIN1 Gene Mutation
    APC Gene Mutation
    Solid Tumor

NCT06005974

Recursion Pharmaceuticals Inc.

13 December 2024

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What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

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The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

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Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

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Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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