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NCT01744691 · ClinicalTrials.gov registry record · Phase 2

A Multicenter Phase 2 Study of Ibrutinib in Patients With Relapsed or Refractory Chronic Lymphocytic Leukemia (CLL) or Small Lymphocytic Lymphoma (SLL) With 17p Deletion

A Phase 2 study, sponsored by Pharmacyclics.

Completed
Registry status
Phase 2
Development phase
145
Enrollment target

NCT01744691: Completed Phase 2 study, sponsored by Pharmacyclics.

NCT01744691 is a Phase 2 study that has completed, run by Pharmacyclics. The registered enrollment target is 145 participants, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01744691, a Phase 2 study, has completed, sponsored by Pharmacyclics.

COMPLETED
Registry status
Phase 2
Development phase
145 participants
Enrollment target

Study Summary

An Open-label, Single arm, Multicenter Phase 2 Study of the Bruton's Tyrosine Kinase Inhibitor ibrutinib in Patients with Relapsed or Refractory Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma with 17p Deletion

Primary Outcome

The primary objective of this study is to evaluate the efficacy of ibrutinib in terms of ORR according to an Independent Review Committee (IRC). ORR based upon IRC assessment is the proportion of responders in the all treated population. Responders were subjects who achieved partial response (PR) or better, ie, complete response (CR), complete response with incomplete marrow recovery (CRi), nodule partial response (nPR) or PR, per IWCLL 2008 criteria with the clarification for treatment-related

Interventions

  • DRUG Ibrutinib

Trial Details

FieldValue
Enrollment Target 145 participants
Start Date 2013-01
Est. Completion 2016-04
Phase Phase 2
Pharmacyclics

54 total trials

What the finished NCT01744691 record still lists

NCT01744691 is an interventional study that assigns participants to a tested intervention. The registered 145 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target.

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

NCT01744691 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01744691 about?

NCT01744691 is a clinical study titled "A Multicenter Phase 2 Study of Ibrutinib in Patients With Relapsed or Refractory Chronic Lymphocytic Leukemia (CLL) or Small Lymphocytic Lymphoma (SLL) With 17p Deletion". An Open-label, Single arm, Multicenter Phase 2 Study of the Bruton's Tyrosine Kinase Inhibitor ibrutinib in Patients with Relapsed or Refractory Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma with 17p Deletion

What is the current status of trial NCT01744691?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 145 participants. The study started on 2013-01. Estimated completion is 2016-04.

What interventions are being tested in trial NCT01744691?

The interventions under investigation include: Ibrutinib (DRUG).

Who is sponsoring clinical trial NCT01744691?

This trial is sponsored by Pharmacyclics, which has 54 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01744691's enrollment target sits among peer trials

145 498th of 2000 higher than 1,501 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 NCT01744691, the US trial registry maintained by the National Library of Medicine. NCT01744691 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.