CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 50 enrolled
Drug / intervention
Smac Mimetic LCL161 +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/NCT02098161
NCT02098161Phase 2Completed

Open Label Phase 2 Single Agent Study of LCL-161 in Patients With Primary Myelofibrosis (PMF), Post-Polycythemia Vera Myelofibrosis (Post-PV MF), or Post-Essential Thrombocytosis Myelofibrosis (Post-ET MF)

M.D. Anderson Cancer Center·interventional·Posted Mar 27, 2014·Updated Jun 6, 2023

In Brief

A Phase 2 clinical trial evaluating Laboratory Biomarker Analysis, Questionnaire Administration, and 1 other intervention for Polycythemia Vera, Post-Polycythemic Myelofibrosis Phase and 2 related conditions. Completed, enrolled 50 participants across 1 site.

Detailed Summary

This phase II trial studies how well second mitochondrial-derived activator of caspases (SMAC) mimetic LCL161 (LCL161) works in treating patients with primary myelofibrosis, post-polycythemia vera myelofibrosis, or post-essential thrombocytosis myelofibrosis. SMAC mimetic LCL161 may help control the growth of abnormal cells by promoting apoptosis (programmed cell death).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

Phase 2CompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedMar 27, 2014
Enrollment StartDec 18, 2014
Primary CompletionMay 19, 2022
TodayJul 2, 2026
Enrollment to primary: 7.4 yearsPosted 12.3 years ago

Interventions

Laboratory Biomarker Analysisother

Correlative studies

Questionnaire Administrationother

Ancillary studies

Smac Mimetic LCL161drug

Given PO