New hope for kids with resistant cancers: experimental drug CUDC-907 enters human testing

NCT ID NCT02909777

First seen Nov 01, 2025 · Last updated Jun 23, 2026 · Updated 32 times

Summary

This early-stage trial tested a new drug called CUDC-907 in 26 children and young adults (ages 1–21) with solid tumors, brain tumors, or lymphoma that had come back or stopped responding to treatment. The main goal was to find safe doses and understand side effects. Researchers also looked at how long the drug stayed in the body and whether it helped control the cancer.

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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

Locations

  • Children's Hospital of Philadelphia

    Philadelphia, Pennsylvania, 19104, United States

  • Dana Farber Cancer Institute

    Boston, Massachusetts, 02115, United States

  • Texas Children's, Baylor College of Medicine

    Houston, Texas, 77030, United States

  • University of California, San Francisco, Benioff Children's Hospital

    San Francisco, California, 94158, United States

What this could mean

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

Active substance

CUDC-907

What this could lead to

If it works, this could point toward a new treatment option for children with cancers that have not responded to standard therapy.

What could go wrong

This is an early Phase 1 trial with only 26 participants, focused on safety and dosing. It is too small to prove effectiveness, and the drug may not work or could have significant side effects.

Conditions

The condition(s) this trial relates to.

brain cancer lymphoma neuroblastoma

As listed by the trial registrant

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