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Completed Phase 2 Interventional Results available

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

ClinicalTrials.gov ID: NCT01744691

Public ClinicalTrials.gov record NCT01744691. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 24, 2026, 7:30 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Open-label, Single Arm, Multicenter Phase 2 Study of the Bruton's Tyrosine Kinase Inhibitor PCI-32765 (Ibrutinib) in Patients With Relapsed or Refractory Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma With 17p Deletion (RESONATE™-17)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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

Study identification

NCT ID
NCT01744691
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pharmacyclics LLC.
Industry
Enrollment
145 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 2013 (Type not available)
Primary completion
Jun 2014 (Actual)
Completion
Apr 2016 (Actual)
Last update posted
Feb 27, 2017

2013 – 2016

United States locations

U.S. sites
18
U.S. states
13
U.S. cities
18
Facility City State ZIP Site status
Not listed Phoenix Arizona — —
Not listed Duarte California — —
Not listed Greenbrae California — —
Not listed La Jolla California — —
Not listed Stanford California — —
Not listed Tampa Florida — —
Not listed Chicago Illinois — —
Not listed Boston Massachusetts — —
Not listed Ann Arbor Michigan — —
Not listed Rochester Minnesota 55905 —
Not listed St Louis Missouri — —
Not listed Hackensack New Jersey — —
Not listed New Hyde Park New York — —
Not listed New York New York — —
Not listed Goldsboro North Carolina — —
Not listed Columbus Ohio — —
Not listed Toldedo Ohio — —
Not listed Houston Texas — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 37 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01744691, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 27, 2017 · Synced Oct 24, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01744691 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →