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

NCT00935987 is a Phase 1 study that has completed, run by Sierra Oncology LLC - a GSK company. The registered enrollment target is 166 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (177% higher). According to ClinicalTrials.gov, the official US trial registry.

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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 finished NCT00935987 record still lists

NCT00935987 is an interventional study that assigns participants to a tested intervention. The registered 166 participants enrollment target is mid-sized for trials with a published cap, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (177% higher).

The record links to 0 conditions, and to 1 intervention - of which CYT387 is the first listed.

NCT00935987 does not publish any study locations in the registry export this page uses.

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.

How this trial's enrollment target compares

Where NCT00935987's enrollment target sits among peer trials

166 330th of 2000 higher than 1,669 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00935987, the US trial registry maintained by the National Library of Medicine. NCT00935987 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.