ClinicalTrials.gov record
Active, not recruiting Phase 3 Interventional Results available

Study of Acalabrutinib (ACP-196) Versus Ibrutinib in Previously Treated Participants With High Risk Chronic Lymphocytic Leukemia (CLL)

ClinicalTrials.gov ID: NCT02477696

Public ClinicalTrials.gov record NCT02477696. 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 May 8, 2026, 10:43 PM EDT

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

Official title

A Randomized, Multicenter, Open-Label, Non-Inferiority, Phase III Study of Acalabrutinib (ACP-196) Versus Ibrutinib in Previously Treated Subjects With High Risk Chronic Lymphocytic Leukemia

Study identification

NCT ID
NCT02477696
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Acerta Pharma BV
Industry
Enrollment
533 participants

Conditions and interventions

Interventions

  • Acalabrutinib Drug
  • Ibrutinib Drug

Drug

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
Jul 27, 2015
Primary completion
Sep 14, 2020
Completion
Jan 2, 2028
Last update posted
Mar 26, 2026

2015 – 2028

United States locations

U.S. sites
31
U.S. states
17
U.S. cities
29
Facility City State ZIP Site status
Research Site Phoenix Arizona 85054
Research Site Anaheim California 92801
Research Site Berkeley California 94704
Research Site Duarte California 91010
Research Site La Jolla California 92093
Research Site Los Angeles California 90095
Research Site Palo Alto California 94304
Research Site Santa Rosa California 95403
Research Site Jacksonville Florida 32224
Research Site Tampa Florida 33612
Research Site Athens Georgia 30607
Research Site Harvey Illinois 60426
Research Site Peoria Illinois 61615
Research Site Wichita Kansas 67214
Research Site Minneapolis Minnesota 55426
Research Site Rochester Minnesota 55905
Research Site Billings Montana 59102
Research Site Hackensack New Jersey ?07601
Research Site Lake Success New York 11042
Research Site New Hyde Park New York 11042
Research Site New York New York 10021
Research Site New York New York 10029
Research Site New York New York 10065
Research Site Durham North Carolina 27710
Research Site Columbus Ohio 43210
Research Site Philadelphia Pennsylvania 19104
Research Site Houston Texas 77030
Research Site Round Rock Texas 78665
Research Site Charlottesville Virginia 22908
Research Site Tacoma Washington 98405
Research Site Northwest WA Wisconsin 20007

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 99 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02477696, 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 Mar 26, 2026 · Synced May 8, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02477696 live on ClinicalTrials.gov.

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