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A Study of ACR-368 in Ovarian Carcinoma, Endometrial Adenocarcinoma, and Urothelial Carcinoma

Researching ACR-368 for ovarian, endometrial, and bladder cancer.

Recruiting
18 years and older
All
Phase 1/2

This study aims to test the safety and effectiveness of a new drug, ACR-368, for treating certain types of cancer. The cancers being studied are ovarian carcinoma (ovarian cancer), endometrial adenocarcinoma (cancer in the lining of the uterus), and urothelial carcinoma (bladder cancer). Participants will take ACR-368 alone or with a very low dose of another drug called gemcitabine. The study uses a special test called OncoSignature® to decide which treatment is best for each person. Patients will stay in the study until their cancer worsens, they experience severe side effects, or they decide to stop. To join, participants need to have specific medical conditions and meet certain requirements, like having a life expectancy of more than three months.

  • Study Length: Until cancer worsens or unacceptable side effects occur.
  • Participants receive either ACR-368 alone or with gemcitabine.
  • Regular health checks and tests will be required.
Study details
    Platinum-resistant Ovarian Cancer
    Endometrial Adenocarcinoma
    Urothelial Carcinoma

NCT05548296

Acrivon Therapeutics

19 April 2025

Step 1 Get in touch with the nearest study center
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  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

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

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