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Low-Dose combo aims to tame bone marrow cancers with fewer side effects

NCT ID NCT05184842

First seen Jan 06, 2026 · Last updated Jun 23, 2026 · Updated 36 times

Summary

This phase 2 trial tests a low-dose weekly schedule of two drugs, decitabine and venetoclax, in people with myelodysplastic syndromes (MDS), acute myeloid leukemia (AML), or chronic myelomonocytic leukemia (CMML). The goal is to see if this gentler approach reduces treatment delays and side effects while still controlling the cancer. About 91 adults will take part.

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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

  • Montefiore Medical Center

    RECRUITING

    The Bronx, New York, 10467, United States

    Contact Phone: •••-•••-••••

  • University of California Davis Health (UC Davis Health)

    RECRUITING

    Sacramento, California, 95817, United States

  • White Plains Hospital

    RECRUITING

    White Plains, New York, 10601, 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

Decitabine and Venetoclax

What this could lead to

If this works, it could offer a gentler treatment option for bone marrow cancers with fewer side effects.

What could go wrong

This is a small, early-phase trial (91 people) focused on tolerability, not yet proven to improve survival or remission rates. The low dose may also be less effective.

Conditions

The condition(s) this trial relates to.

acute myeloid leukemia chronic myelomonocytic leukemia Myelodysplastic Syndromes

As listed by the trial registrant

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