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Active, not recruiting Phase 3 Interventional

A Combination of Acalabrutinib With R-CHOP in Subjects With Previously Untreated Non-GCB DLBCL (ACE-LY-312)

ClinicalTrials.gov ID: NCT04529772

Public ClinicalTrials.gov record NCT04529772. 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 Nov 3, 2026, 10:14 AM EST

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

Official title

Phase 3, Randomized, Double-Blind, Placebo-Controlled Study of Acalabrutinib in Combination With Rituximab, Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone (R-CHOP) in Subjects ≤75 Years With Previously Untreated Non-GCB DLBCL

Brief summary

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

Phase 3 randomized, double-blind, placebo-controlled, study assessing the efficacy and safety of acalabrutinib plus rituximab,cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) vs placebo plus R-CHOP in subjects ≤75 years of age with previously untreated non-germinal center diffuse large B-cell lymphoma.

Study identification

NCT ID
NCT04529772
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Acerta Pharma BV
Industry
Enrollment
611 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 75 Years
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
Oct 8, 2020 (Actual)
Primary completion
Feb 22, 2027 (Estimated)
Completion
Feb 22, 2027 (Estimated)
Last update posted
Oct 13, 2026

2020 – 2027

United States locations

U.S. sites
32
U.S. states
21
U.S. cities
31
Facility City State ZIP Site status
Research Site Tucson Arizona 85711 —
Research Site Little Rock Arkansas 72205 —
Research Site Irvine California 92618 —
Research Site Aurora Colorado 80012 —
Research Site Norwich Connecticut 06360 —
Research Site Fort Myers Florida 33901 —
Research Site Orlando Florida 32804 —
Research Site St. Petersburg Florida 33705-1449 —
Research Site Tallahassee Florida 32308-5304 —
Research Site West Palm Beach Florida 33401 —
Research Site Fort Wayne Indiana 46845 —
Research Site Des Moines Iowa 50309 —
Research Site Wichita Kansas 67214 —
Research Site Louisville Kentucky 40207 —
Research Site Baltimore Maryland 21201 —
Research Site Grand Rapids Michigan 49503 —
Research Site Minneapolis Minnesota 55407 —
Research Site St Louis Missouri 63129 —
Research Site Albany New York 12208 —
Research Site New York New York 10028 —
Research Site New York New York 10065 —
Research Site Stony Brook New York 11795 —
Research Site Charlotte North Carolina 28204 —
Research Site Winston-Salem North Carolina 27103 —
Research Site Eugene Oregon 97401 —
Research Site Portland Oregon 97239 —
Research Site Philadelphia Pennsylvania 19111 —
Research Site Pittsburgh Pennsylvania 15212 —
Research Site Nashville Tennessee 37203 —
Research Site Fort Sam Houston Texas 78234 —
Research Site Lubbock Texas 79410 —
Research Site Salem Virginia 24153 —

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 213 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04529772, 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 Oct 13, 2026 · Synced Nov 3, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04529772 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →