Description:
The purpose of this study is to evaluate the efficacy and safety of acalabrutinib in
combination with venetoclax and acalabrutinib in combination with venetoclax with and without
obinutuzumab compared to chemoimmunotherapy in subjects with previously untreated CLL.
Title
- Brief Title: Study of Acalabrutinib (ACP-196) in Combination With Venetoclax (ABT-199), With and Without Obinutuzumab (GA101) Versus Chemoimmunotherapy for Previously Untreated CLL
- Official Title: A Randomized, Multicenter, Open-Label, Phase 3 Study to Compare the Efficacy and Safety of Acalabrutinib (ACP-196) in Combination With Venetoclax With and Without Obinutuzumab Compared to Investigator's Choice of Chemoimmunotherapy in Subjects With Previously Untreated Chronic Lymphocytic Leukemia Without Del(17p) or TP53 Mutation
Clinical Trial IDs
- ORG STUDY ID:
ACE-CL-311
- SECONDARY ID:
D8221C00001
- NCT ID:
NCT03836261
Conditions
- Chronic Lymphocytic Leukemia
Interventions
| Drug | Synonyms | Arms |
|---|
| Acalabrutinib | Calquence (acalabrutinib) | Acalabrutinib, Venetoclax |
| Venetoclax | Venclyxto, Venclexta | Acalabrutinib, Venetoclax |
| Chemoimmunotherapy | | Chemoimmunotherapy |
| Obinutuzumab | Gazyva, Gazyvaro | Acalabrutinib, Venetoclax, Obinutuzumab |
Purpose
The purpose of this study is to evaluate the efficacy and safety of acalabrutinib in
combination with venetoclax and acalabrutinib in combination with venetoclax with and without
obinutuzumab compared to chemoimmunotherapy in subjects with previously untreated CLL.
Detailed Description
This randomized, global, multicenter, open-label, Phase 3 study will evaluate the efficacy
and safety of AV and AVG versus chemoimmunotherapy (FCR or BR) in subjects with previously
untreated CLL without del(17p) or TP53. Subjects will be randomized in a 1:1:1 ratio into 3
arms through a block stratified randomization procedure.
The study includes screening (35 days), treatment (from randomization until study drug
discontinuation) and follow-up phase.
Trial Arms
| Name | Type | Description | Interventions |
|---|
| Acalabrutinib, Venetoclax | Experimental | Acalabrutinib in combination with Venetoclax | |
| Acalabrutinib, Venetoclax, Obinutuzumab | Experimental | Acalabrutinib in combination with Venetoclax with or without Obinutuzumab | - Acalabrutinib
- Venetoclax
- Obinutuzumab
|
| Chemoimmunotherapy | Active Comparator | Chemoimmunotherapy
FCR: Fludarabine, Cyclophosphamide and Rituximab | |
Eligibility Criteria
Inclusion Criteria:
- Men and women ≥18 years of age.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0-2.
- Diagnosis of CLL that meets published diagnostic criteria (Hallek et al. 2018)
- Active disease per IWCLL 2018 criteria that requires treatment.
- Participants must use highly effective birth control throughout the study.
Exclusion Criteria:
- Any prior CLL-specific therapies.
- Detected del(17p) or TP53 mutation.
- Transformation of CLL to aggressive non-Hodgkin lymphoma (NHL) (e.g., Richter's
transformation, prolymphocytic leukemia [PLL], or diffuse large B cell lymphoma
[DLBCL]), or central nervous system (CNS) involvement by leukemia.
- History of confirmed progressive multifocal leukoencephalopathy (PML).
- Received any investigational drug within 30 days before first dose of study drug.
- Major surgical procedure within 30 days before the first dose of study drug.
- Significant cardiovascular disease such as symptomatic arrhythmias, congestive heart
failure, or myocardial infarction within 6 months of Screening, or any Class 3 or 4
cardiac disease. Note: Subjects with controlled, asymptomatic atrial fibrillation are
allowed to enroll on study.
- Malabsorption syndrome, disease significantly affecting gastrointestinal function, or
resection of the stomach, or extensive small bowel resection that is likely to affect
absorption, symptomatic inflammatory bowel disease, or partial or complete bowel
obstruction, or gastric restrictions and bariatric surgery, such as gastric bypass.
- Received a live virus vaccination within 28 days of first dose of study drug.
- Known history of infection with human immunodeficiency virus (HIV).
- Serologic status reflecting active hepatitis B or C infection.
- History of known hypersensitivity or anaphylactic reactions to study drugs or
excipients.
- History of stroke or intracranial hemorrhage within 6 months before first dose of
study drug.
- Known bleeding disorders.
- Requires or receiving anticoagulation with warfarin or equivalent vitamin K
antagonists.
- Female participants must not be breastfeeding or pregnant.
- Concurrent participation in another therapeutic clinical trial.
| Maximum Eligible Age: | 130 Years |
| Minimum Eligible Age: | 18 Years |
| Eligible Gender: | All |
| Healthy Volunteers: | No |
Primary Outcome Measures
| Measure: | To evaluate the efficacy of acalabrutinib with venetoclax (Arm A) compared to chemoimmunotherapy fludarabine/cyclophosphamide/rituximab [FCR] or bendamustine/rituximab [BR] (Arm C): PFS |
| Time Frame: | 6 years |
| Safety Issue: | |
| Description: | Progression-free survival (PFS) after randomization, defined as the time from randomization to the first occurrence of disease progression or death from any cause (whichever occurs first), as determined by the Independent Review Committee (IRC) according to the International Workshop on Chronic Lymphocytic Leukemia (IWCLL) 2018 criteria |
Secondary Outcome Measures
| Measure: | To evaluate the efficacy of acalabrutinib with venetoclax in combination with obinutuzumab (Arm B) compared with FCR or BR (Arm C): PFS |
| Time Frame: | 6 years |
| Safety Issue: | |
| Description: | PFS after randomization, defined as the time from randomization to the first occurrence of disease progression or death from any cause (whichever occurs first), as determined by the IRC assessment and investigator assessment |
| Measure: | To evaluate the efficacy of acalabrutinib with venetoclax (Arm A) compared with FCR or BR (Arm C): PFS defined the same as above per investigator assessment. |
| Time Frame: | 6 years |
| Safety Issue: | |
| Description: | PFS after randomization, defined as the time from randomization to the first occurrence of disease progression or death from any cause (whichever occurs first), as determined by the IRC assessment and investigator assessment |
Details
| Phase: | Phase 3 |
| Primary Purpose: | Interventional |
| Overall Status: | Recruiting |
| Lead Sponsor: | Acerta Pharma BV |
Trial Keywords
- CLL
- Chronic Leukemia Lymphocytic
- Leukemia
Last Updated
May 24, 2021
