Tailored chemo dosing aims to boost stem cell transplant success in myeloma

NCT ID NCT04483206

First seen Jun 17, 2026 · Last updated Jun 21, 2026 · Updated 1 time

Summary

This phase 1 trial is testing a new way to dose the chemotherapy drug melphalan for people with multiple myeloma who are getting a stem cell transplant. Instead of a standard dose, the amount is personalized based on each patient's blood levels after a test dose. The goal is to find the best dose that kills cancer cells while limiting side effects like mouth sores and heart rhythm problems. The study involves 90 participants and will also check if the treatment leads to deeper cancer remission.

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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

  • University Illinois Chicago

    NOT_YET_RECRUITING

    Chicago, Illinois, 60607, United States

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

  • Winship Cancer Institute of Emory University

    RECRUITING

    Atlanta, Georgia, 30322, United States

    Contact

    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

Melphalan (chemotherapy drug)

What this could lead to

If successful, this could lead to more precise melphalan dosing for multiple myeloma patients, potentially improving treatment effectiveness and reducing severe side effects like mouth sores.

What could go wrong

This is an early phase 1 trial with only 90 participants, so results may not apply broadly. The personalized dosing approach is experimental and may not improve outcomes or reduce toxicity as hoped.

Conditions

The condition(s) this trial relates to.

extramedullary plasmacytoma heavy chain disease non-amyloid monoclonal immunoglobulin deposition disease plasma cell myeloma plasma cell neoplasm

As listed by the trial registrant

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