drugset / Trial / NCT04985656

A Study of Pevonedistat Combined With Decitabine and Cedazuridine in Adults With Higher-risk Myelodysplastic Syndromes

NCT04985656

Phase 2 Withdrawn Takeda
NaSingle-groupOpen-labelTreatment

Summary

The main aim of the study is to see if signs and symptoms of myelodysplastic syndromes disappear when treated with pevonedistat combined with decitabine and cedazuridine. Participants will receive an infusion of pevonedistat 3 times during a 28-day cycle. They will also take decitabine and cedazuridine tablets once a day for the first 5 days of the same cycle. A minimum of 6 28-day cycles is recommended, but participants can stop treatment at any time. A bone marrow biopsy, bone marrow aspirates, and blood samples will be collected during the study. Participants will attend a follow-up visit 30 days after their last dose of pevonedistat. Once treatment has ended, participants will be followed up with either monthly clinic visits or will be contacted every 3 months.

Timeline

Start
2021-10-01
Primary completion
2024-01-08
Completion
2024-11-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Cedazuridine Small molecule 100 mg Oral
Subject Decitabine Small molecule 35 mg Oral
Subject Pevonedistat Small molecule 20 mg/m2 Intravenous