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

NCT00935987 · ClinicalTrials.gov registry record · Phase 1

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

A Phase 1 study, sponsored by Sierra Oncology LLC - a GSK company.

Completed
Registry status
Phase 1
Development phase
166
Enrollment target

NCT00935987 is a Phase 1 study that has completed, run by Sierra Oncology LLC - a GSK company. The registered enrollment target is 166 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00935987, a Phase 1 study, has completed, sponsored by Sierra Oncology LLC - a GSK company.

COMPLETED
Registry status
Phase 1
Development phase
166 participants
Enrollment target

Study Summary

This study seeks to (i) determine a safe and tolerated dose of CYT387 (momelotinib) given to patients with PMF, post-PV or post-ET and, (ii) assess the effectiveness of orally-administered CYT387 as a treatment for PMF, post-PV or post-ET.

Interventions

  • DRUG CYT387

Trial Details

FieldValue
Enrollment Target 166 participants
Start Date 2009-11
Est. Completion 2012-04
Phase Phase 1

What the Registry Record Tells You About NCT00935987

The ClinicalTrials.gov registry entry for NCT00935987 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 166 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 CYT387 is the first listed.

NCT00935987 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00935987 about?

NCT00935987 is a clinical study titled "Safety and Efficacy Study of CYT387 in Primary Myelofibrosis (PMF) or Post-polycythemia Vera (PV) or Post-essential Thrombocythemia (ET)". This study seeks to (i) determine a safe and tolerated dose of CYT387 (momelotinib) given to patients with PMF, post-PV or post-ET and, (ii) assess the effectiveness of orally-administered CYT387 as a treatment for PMF, post-PV or post-ET.

What is the current status of trial NCT00935987?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 166 participants. The study started on 2009-11. Estimated completion is 2012-04.

What interventions are being tested in trial NCT00935987?

The interventions under investigation include: CYT387 (DRUG).

Who is sponsoring clinical trial NCT00935987?

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.