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NCT01371617 · ClinicalTrials.gov registry record · Phase 2

A Phase 2 Study With IPI-926 in Patients With Myelofibrosis

A Phase 2 study, sponsored by Infinity Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
14
Enrollment target

NCT01371617: Completed Phase 2 study, sponsored by Infinity Pharmaceuticals.

NCT01371617 is a Phase 2 study that has completed, run by Infinity Pharmaceuticals. The registered enrollment target is 14 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (89% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01371617, a Phase 2 study, has completed, sponsored by Infinity Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
14 participants
Enrollment target

Study Summary

The purpose of this study is to determine the safety and efficacy of IPI-926 in patients with myelofibrosis (MF) (primary myelofibrosis \[PMF\], post-polycythemia vera myelofibrosis \[post-PV MF\], or post-essential thrombocythemia myelofibrosis \[post-ET MF\]).

Interventions

  • DRUG IPI-926

Trial Details

FieldValue
Enrollment Target 14 participants
Start Date 2011-10
Est. Completion 2012-08
Phase Phase 2
Infinity Pharmaceuticals

17 total trials

What the finished NCT01371617 record still lists

NCT01371617 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 14 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (89% lower).

The record links to 0 conditions, and to 1 intervention - of which IPI-926 is the first listed.

NCT01371617 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01371617 about?

NCT01371617 is a clinical study titled "A Phase 2 Study With IPI-926 in Patients With Myelofibrosis". The purpose of this study is to determine the safety and efficacy of IPI-926 in patients with myelofibrosis (MF) (primary myelofibrosis \[PMF\], post-polycythemia vera myelofibrosis \[post-PV MF\], or post-essential thrombocythemia myelofibrosis \[post-ET MF\]).

What is the current status of trial NCT01371617?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 14 participants. The study started on 2011-10. Estimated completion is 2012-08.

What interventions are being tested in trial NCT01371617?

The interventions under investigation include: IPI-926 (DRUG).

Who is sponsoring clinical trial NCT01371617?

This trial is sponsored by Infinity Pharmaceuticals, which has 17 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01371617's enrollment target sits among peer trials

14 1941st of 2000 higher than 54 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT01371617, the US trial registry maintained by the National Library of Medicine. NCT01371617 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.