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Experimental drug cocktail aims to outsmart childhood cancers

NCT ID NCT04308330

First seen Apr 23, 2026 · Last updated Jun 22, 2026 · Updated 12 times

Summary

This early-phase trial tests a four-drug combination—vorinostat plus three chemotherapy drugs—in children, teens, and young adults up to age 30 whose solid tumors or brain cancers have returned or not responded to standard treatment. The main goal is to find the safest dose of vorinostat when used with the other drugs, and to see what side effects occur. Up to 30 participants will be enrolled.

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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: •••••@•••••

  • Contact

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

Locations

  • New York Medical College

    RECRUITING

    Valhalla, New York, 10595, United States

    Contact

    Contact

What this could mean

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

Active substance

vorinostat (Zolinza) combined with vincristine, irinotecan, and temozolomide

What this could lead to

If it works, this could point toward a new treatment option for children and young adults with hard-to-treat cancers that have come back or not responded to standard therapy.

What could go wrong

This is a very early Phase 1 trial with only 30 participants, focused on finding a safe dose. The combination may not shrink tumors or could cause severe side effects.

Conditions

The condition(s) this trial relates to.

Ewing sarcoma hepatoblastoma Neoplasms, Germ Cell and Embryonal neuroblastoma rhabdomyosarcoma Wilms tumor

As listed by the trial registrant

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