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New hope for endometrial cancer: targeted drug plus chemo shows promise

NCT ID NCT07170982

First seen Oct 31, 2025 · Last updated Jun 22, 2026 · Updated 30 times

Summary

This phase 2 trial tests whether adding the targeted drug fruquintinib to standard chemotherapy (paclitaxel and carboplatin) works better than chemo alone for advanced or recurrent endometrial cancer that is mismatch repair-proficient (pMMR). About 128 participants will be randomly assigned to receive either the combo or chemo alone. The goal is to see if the combo shrinks tumors more effectively and delays cancer growth.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • Department of Gynecologic Oncology, Sun Yat-sen University Cancer Center

    Guangzhou, Guangdong, 510060, China

    Contact Phone: •••-•••-•••• Email: •••••@•••••

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance

fruquintinib (a targeted cancer drug taken orally) combined with paclitaxel and carboplatin (standard chemotherapy)

What this could lead to

If successful, this could offer a new first-line treatment option for advanced pMMR endometrial cancer, potentially improving tumor shrinkage and delaying disease progression.

What could go wrong

This is an early phase 2 trial with only 128 participants, so results may not be definitive. The drug combination may cause side effects or fail to show benefit over standard chemo alone.

Conditions

The condition(s) this trial relates to.

endometrium neoplasm

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.