Gene test could tailor chemo doses for rare cancer

NCT ID NCT06406465

First seen Jun 27, 2026 · Last updated Aug 14, 2026 · Updated 34 times

Summary

This phase 2 trial is testing whether adjusting the dose of the drug belinostat based on a person's genetics can make treatment safer and more effective for high-grade neuroendocrine carcinoma. About 60 adults will receive belinostat along with two other chemotherapy drugs, cisplatin and etoposide. The goal is to see if genetic testing can help doctors give the right dose to each patient.

What this could mean

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

Active substance
belinostat, cisplatin, etoposide
What this could lead to
If successful, this could lead to personalized dosing of belinostat based on a person's genetics, making treatment safer and more effective for high-grade neuroendocrine cancer.
What could go wrong
This is a small, early-phase trial with only 60 participants. The genetic approach may not improve outcomes, and the drugs have significant side effects like low blood counts and organ damage.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • National Institutes of Health Clinical Center

    RECRUITING

    Bethesda, Maryland, 20892, United States

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