drugset / Trial / NCT05013437

Melphalan on Disease Burden Measured by Next Generation Sequencing Before AHCT (Autologous Hematopoietic Cell Transplant) for Multiple Myeloma

NCT05013437

Phase 0 Withdrawn Koen van Besien
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to see if Multiple Myeloma (MM) cells are sensitive to the chemotherapy used in transplant or not. The main chemotherapy agent utilized in stem cell transplant is melphalan. The study will utilize 1/10 of the dose used in transplant to study sensitivity of the tumor to melphalan. Melphalan is approved by the U.S. Food and Drug Administration (FDA) for transplant for MM patients.

Timeline

Start
2023-09
Primary completion
2023-12
Completion
2024-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Melphalan Small molecule 16 mg/m2 Intravenous
Background Acetaminophen Small molecule 650 mg Oral
Background Diphenhydramine Unknown 50 mg Intravenous
Background Prochlorperazine Small molecule 10 mg Intravenous

Indications