Tamibarotene Plus Azacitidine in Participants With Newly Diagnosed RARA-positive Higher-Risk Myelodysplastic Syndrome

Stopped early · Phase 3 · Has a placebo group

Conditions studied: Myelodysplastic Syndromes

In brief

This study compares the efficacy of Tamibarotene in combination with azacitidine to azacitidine in combination with placebo in participants who are Retinoic Acid Receptor Alpha (RARA) positive, and newly diagnosed with higher-risk myelodysplastic syndrome (HR-MDS), and who have not received treatment for this diagnosis. The primary goal of the study is to compare the complete remission rate between the two treatment arms.

Key facts

Study ID
NCT04797780
Run by
Syros Pharmaceuticals
People needed
246
Starts
2021-02-08
Expected to finish
2024-11-13
Last updated by the study team
2025-04-10

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

Where it is running

Full record on ClinicalTrials.gov

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