Condition: Myelodysplastic Syndromes · Anemia · Sponsor: Halia Therapeutics, Inc.
The primary objective of this study is to evaluate the efficacy and safety of ofirnoflast administered orally once daily in adults with very low- to intermediate-risk myelodysplastic syndromes (MDS) who are transfusion-dependent and have failed one to three prior therapies, in order to identify the optimal dose for continuation into a Phase 3 study. The secondary objectives of this study are to evaluate the extended hematologic response to ofirnoflast, to assess the safety and tolerability of ofirnoflast during the dose-selection phase, and to evaluate hematologic improvement with ofirnoflast treatment.
This description comes directly from the study's public registry record.
Associate Medical Director · 385-355-4315 · monitor@haliatx.com
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Source record: clinicaltrials.gov/study/NCT07738510