For Healthcare Professionals

Acalabrutinib (ACP-196), a Btk Inhibitor, for Treatment of de Novo Activated B-cell (ABC) Subtype of Diffuse Large B-Cell Lymphoma

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About the study

To characterize the safety profile of acalabrutinib in subjects with relapsed or refractory de Novo Activated B-cell (ABC) Subtype of Diffuse Large B-Cell Lymphoma (DLBCL).
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Inclusion Criteria:


  1. Men and women ≥ 18 years of age.
  2. Pathologically confirmed de novo ABC DLBCL
  3. Relapsed or refractory disease
  4. Subjects must have ≥ 1 measurable disease sites

EXCLUSION CRITERIA

Exclusion Criteria:


  1. A life-threatening illness, medical condition or organ system dysfunction which, in the investigator's opinion, could compromise the subject's safety, interfere with the absorption or metabolism of acalabrutinib, or put the study outcomes at undue risk
  2. Significant cardiovascular disease such as uncontrolled or symptomatic arrhythmias, congestive heart failure, or myocardial infarction within 6 months of screening, or any Class 3 or 4 cardiac disease as defined by the New York Heart Association Functional Classification, or LVEF < 50%
  3. Malabsorption syndrome, disease significantly affecting gastrointestinal function, or resection of the stomach or small bowel or ulcerative colitis, symptomatic inflammatory bowel disease, or partial or complete bowel obstruction.
  4. Breast feeding or pregnant

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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.

Study’s details


Contition

Activated B-cell Diffuse Large B-Cell Lymphoma (ABC DLBCL)

Age (in years)

18 - 130

Phase

Phase 1

Participants needed

21

Est. Completion Date

Apr 1, 2026

Treatment type

Interventional


Sponsor

Acerta Pharma BV

ClinicalTrials.gov identifier

NCT02112526

Study number

ACE-LY-002

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