CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 121 enrolled
Drug / intervention
Azacitidine +2 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01787487
NCT01787487Phase 2Completed

Evaluation of Ruxolitinib and Azacytidine Combination as a Therapy for Patients With Myelofibrosis and Myelodysplastic Syndrome/ Myeloproliferative Neoplasm

M.D. Anderson Cancer Center·interventional·Posted Feb 8, 2013·Updated Mar 31, 2026

In Brief

A Phase 2 clinical trial evaluating Azacitidine, Laboratory Biomarker Analysis, and 1 other intervention for Myelodysplastic/Myeloproliferative Neoplasm, Unclassifiable and 3 related conditions. Completed, enrolled 121 participants across 1 site.

Detailed Summary

This phase II trial studies how well ruxolitinib phosphate and azacytidine work in treating patients with myelofibrosis or myelodysplastic syndrome/myeloproliferative neoplasm. Ruxolitinib phosphate may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as azacytidine, work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving ruxolitinib phosphate and azacytidine may be an effective treatment for myelofibrosis or myelodysplastic syndrome/myeloproliferative neoplasm.

Study Details

Timeline

Phase 2CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedFeb 8, 2013
Enrollment StartMar 13, 2013
Primary CompletionJan 20, 2026
TodayJul 2, 2026
Enrollment to primary: 12.9 yearsPosted 13.4 years ago

Interventions

Azacitidinedrug

Given SC or IV

Laboratory Biomarker Analysisother

Correlative studies

Ruxolitinib Phosphatedrug

Given PO