ClinicalTrials.gov record
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 May 8, 2026, 10:48 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

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

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

Interventions

  • Cyclophosphamide Drug
  • Doxorubicin Drug
  • Prednisone Drug
  • Rituximab Drug
  • Vincristine Drug
  • acalabrutinib Drug
  • placebo Drug

Drug

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 7, 2020
Primary completion
Feb 21, 2027
Completion
Feb 21, 2027
Last update posted
Mar 30, 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 211 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 Mar 30, 2026 · Synced May 8, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04529772 live on ClinicalTrials.gov.

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