Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01236638 · ClinicalTrials.gov registry record · Phase 2

Extension Study Evaluating the Long Term Safety and Efficacy Study of CYT387 in Primary Myelofibrosis (PMF) or Post-polycythemia Vera (PV) or Post-essential Thrombocythemia (ET)

A Phase 2 study, sponsored by Sierra Oncology LLC - a GSK company.

Completed
Registry status
Phase 2
Development phase
120
Enrollment target

NCT01236638 is a Phase 2 study that has completed, run by Sierra Oncology LLC - a GSK company. The registered enrollment target is 120 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01236638, a Phase 2 study, has completed, sponsored by Sierra Oncology LLC - a GSK company.

COMPLETED
Registry status
Phase 2
Development phase
120 participants
Enrollment target

Study Summary

This extension protocol to the core study CCL09101 allows patients who have tolerated the drug and derived a clinical benefit, to continue to receive treatment beyond the 9 cycles of the core protocol. Long term safety and efficacy of CYT387 (momelotinib) will be evaluated.

Interventions

  • DRUG Momelotinib

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2010-11
Est. Completion 2014-06
Phase Phase 2

What the Registry Record Tells You About NCT01236638

The ClinicalTrials.gov registry entry for NCT01236638 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 120 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Sierra Oncology LLC - a GSK company, which has 17 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Momelotinib is the first listed.

NCT01236638 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01236638 about?

NCT01236638 is a clinical study titled "Extension Study Evaluating the Long Term Safety and Efficacy Study of CYT387 in Primary Myelofibrosis (PMF) or Post-polycythemia Vera (PV) or Post-essential Thrombocythemia (ET)". This extension protocol to the core study CCL09101 allows patients who have tolerated the drug and derived a clinical benefit, to continue to receive treatment beyond the 9 cycles of the core protocol. Long term safety and efficacy of CYT387 (momelotinib) will be evaluated.

What is the current status of trial NCT01236638?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 120 participants. The study started on 2010-11. Estimated completion is 2014-06.

What interventions are being tested in trial NCT01236638?

The interventions under investigation include: Momelotinib (DRUG).

Who is sponsoring clinical trial NCT01236638?

This trial is sponsored by Sierra Oncology LLC - a GSK company, which has 17 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.