CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 100 enrolled
Drug / intervention
Omacetaxine mepesuccinatedrug
Likely dose
Omacetaxine mepesuccinate 1.25mgfrom 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/NCT00462943
NCT00462943Phase 2Completed

A Phase II Open-Label Study of the Subcutaneous Administration of Homoharringtonine. (Omacetaxine Mepesuccinate; OMA) in the Treatment of Patients With Chronic Myeloid. Leukemia (CML) Who Have Failed or Are Intolerant to Tyrosine Kinase Inhibitor Therapy

Teva Branded Pharmaceutical Products R&D, Inc.·interventional·Posted Apr 19, 2007·Updated Dec 28, 2021

In Brief

A Phase 2 clinical trial evaluating Omacetaxine mepesuccinate for Chronic Myeloid Leukemia. Completed, enrolled 100 participants across 29 sites in 10 countries.

Detailed Summary

A Phase II open-label trial of subcutaneous HHT (omacetaxine mepesuccinate) in the treatment of patients who are resistant to or intolerant to Tyrosine Kinase Inhibitors.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada, France, Germany, Hungary, India, Italy, Poland, Singapore, United Kingdom, United States

Timeline

Phase 2CompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedApr 19, 2007
Enrollment StartMar 7, 2007
Primary CompletionAug 4, 2009
Study CompletionJun 27, 2013
TodayJul 2, 2026
Enrollment to primary: 2.4 yearsPosted 19.2 years ago

Interventions

Omacetaxine mepesuccinatedrug

Induction: 1.25mg/m\^2 subcutaneously twice daily for 14 consecutive days, every 28 days. Maintenance: 1.25mg/m\^2 subcutaneously twice daily for 7 consecutive days, every 28 days. Response targets during induction vary by chronic myeloid leukemia (CML) subclass (chronic, accelerated, or blast phase). Participants will complete at least one cycle (14 days treatment of a 28 day cycle) of induction therapy before changing to maintenance therapy. Participants not demonstrating evidence of clinical response after 6 induction cycles will be considered for removal from the study.