CI

At a glance

ClinicalIndex Comparison Record
Phase 2Terminated· 3 enrolled
Drug / intervention
Pacritinib +2 moredrug
Likely dose
Pacritinib 200 mgfrom 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/NCT02469415
NCT02469415Phase 2Terminated
Terminated

Phase II Study of Pacritinib for Patients With Lower-Risk Myelodysplastic Syndromes

M.D. Anderson Cancer Center·interventional·Posted Jun 11, 2015·Updated Oct 16, 2018

In Brief

A Phase 2 clinical trial evaluating Pacritinib, 5-azacitidine, and 1 other intervention for Leukemia. Terminated early, enrolled 3 participants across 1 site.

Signals

Trial was terminated early

Detailed Summary

The goal of this clinical research study is to learn if pacritinib, either alone or in combination with azacitidine or decitabine, can help to control MDS. The safety of this drug and drug combination will also be studied.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsLeukemia
CountriesUnited States
CollaboratorsCTI BioPharma

Timeline

Phase 2TerminatedFinished
20162017201820192020202120222023202420252026
First PostedJun 11, 2015
Enrollment StartSep 30, 2015
Primary CompletionJun 3, 2017
TodayJul 1, 2026
Enrollment to primary: 1.7 yearsPosted 11.1 years ago

Interventions

Pacritinibdrug

Part 1: Pacritinib 200 mg taken by mouth twice daily. Part 2: Pacritinib dose decreased to 200 mg in the morning and 100 mg in the evening for the first cycle of combined therapy. If no toxicity is observed in first cycle of combined therapy, Pacritinib dose may be increased to 200 mg twice a day on subsequent cycles of combined therapy.

5-azacitidinedrug

Part 2 Starting Dose of 5-azacitidine: 75 mg/m2 by vein on Days 1 - 5 of Cycles 5 and beyond.

Decitabinedrug

Part 2 Starting Dose of Decitabine: 20 mg/m2 by vein on on Days 1 - 7 of Cycles 5 and beyond.