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Chronic Lymphocytic LeukemiaPhase 3NCT05197192

A Phase-3-trial of Acalabrutinib, Obinutuzumab & Venetoclax Compared to Obinutuzumab and Venetoclax in Previously Untreated Patients With High Risk CLL

A Phase 3 study testing Obinutuzumab, Venetoclax and Acalabrutinib in people with Chronic Lymphocytic Leukemia, run by German CLL Study Group at 30 sites in Germany.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
Search all trials

Trial summary

This multicenter, prospective, open-label, randomized, superiority phase 3 study is designed to demonstrate that treatment with a triple combination of acalabrutinib, obinutuzumab and venetoclax (GAVe) prolong the progression-free survival (PFS) as compared to treatment with the combination of obinutuzumab and… Read more about this study

Who is it for?
Ages 18 to 120 years
Conditions the study is for
Chronic Lymphocytic Leukemia
What is being tested?
Obinutuzumab, Venetoclax and Acalabrutinib
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
202 participants
Where
30 sitesGermany
Study dates
19 Apr 2022to May 2028
Phase
Phase 3
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 120 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Documented CLL/SLL requiring treatment according to iwCLL criteria
  • Age at least 18 years
  • At least one of the following risk factors: 17p-deletion, TP53-mutation, complex karyotype (defined as defined as the presence of 3 or more chromosomal aberrations in 2 or more metaphases) or an unmutated IGHV gene status.
  • Life expectancy ≥ six months
  • Adequate bone marrow function indicated by a platelet count >30 x10^9/l
  • Creatinine clearance ≥ 30ml/min
Show all 10Show fewer
  • Adequate liver function as indicated by a total bilirubin ≤ 2 x, AST/ ALT ≤ 2.5 x the institutional ULN value, unless directly attributable to the patient's CLL or to Gilbert's Syndrome
  • Negative testing for hepatitis B (HbsAg negative and anti-HBc negative; patients positive for anti-HBc may be included if PCR for HBV DNA is negative and HBV-DNA PCR is performed every month until 12 months after last treatment cycle),or hepatitis C (negative testing for hepatitis C RNA within 6 wee
  • ks prior to registration for study screening (i.e. PCR only required when serology was positive))
  • ECOG (Eastern Cooperative Oncology Group Performance Status) status 0-2

Who cannot join

  • Any prior CLL-specific therapies (except corticosteroid treatment administered due to necessary immediate intervention; within the last 10 days before start of study treatment, only dose equivalents up to 20 mg prednisolone are permitted)
  • Absence of high risk disease (17p-deletion, TP53-mutation complex karyotype
  • An individual organ/system impairment score of 4 as assessed by the CIRS definition (e.g. advanced cardiac disease (NYHA class 3 or 4) limiting the ability to receive the study treatment or any other life-threatening illness, medical condition or organ system dysfunction that, in the investigator´s opinion, could compromise the patients safety or interfere with the absorption or metabolism of the study drugs (e.g. inability to swallow tablets or impaired resorption in the gastrointestinal tract)
  • Transformation of CLL (Richter transformation)
  • Malignancies other than CLL currently requiring systemic therapies
  • Uncontrolled or active infection of HIV/PML or any other active infection
  • Anticoagulant therapy with warfarin or phenoprocoumon
  • Pregnant women and nursing mothers

Trial locations and contacts

30 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Barbara Eichhorst, MD, Prof. contact

+4922147888220

barbara.eichhorst@uk-koeln.de

30 sites in 1 country

Germany30 sites, 30 recruiting
  • Helios Klinikum Bad Saarow

    Bad Saarow, 15526

    Daniel Schöndube

    Recruiting
  • DRK Kliniken Berlin Köpenick

    Berlin, 12559

    Christian Neumann

    Recruiting
  • Ev. Diakoniekrankenhaus

    Bremen, 28239

    Ralf Ulrich Trappe

    Recruiting
  • Universitätsklinik Köln

    Cologne, 50937

    Barbara Eichhorst

    Recruiting
  • St. Johannes Hospital

    Dortmund, 44137

    Ralf Meyer

    Recruiting
  • Marien Hospital Düsseldorf

    Düsseldorf, 40479

    Stefanie Gröpper

    Recruiting
  • St. Antonius-Hospital

    Eschweiler, 52249

    Peter Staib

    Recruiting
  • Universitaetsklinikum Essen

    Essen, 45147

    Julia von Tresckow

    Recruiting
  • Katholisches Krankenhaus Hagen - St. Josefs Hospital

    Hagen, 58097

    Doris Kraemer

    Recruiting
  • Universitaetskliniken des Saarlandes

    Homburg, 66424

    Jörg Bittenbring

    Recruiting
  • Klinikum Idar-Oberstein SHG

    Idar-Oberstein, 55743

    Johannes Schneider

    Recruiting
  • Staedtisches Klinikum Karlsruhe

    Karlsruhe, 76133

    Henriette Huber

    Recruiting
  • Universitaetsklinikum Schleswig-Holstein Campus Kiel

    Kiel, 24116

    Matthias Ritgen

    Recruiting
  • Klinikum Landshut

    Landshut, 84034

    Christian Bogner

    Recruiting
  • Klinikum Lippe-Lemgo

    Lemgo, 32657

    Karin Heinisch

    Recruiting
  • St Vincenz Krankenhaus

    Limburg, 65549

    Thomas Neuhaus

    Recruiting
  • Universitaetsklinikum Magdeburg

    Magdeburg, 39120

    Ana Maria Waldleben

    Recruiting
  • Klinikum Hochsauerland - St. Walburga Krankenhaus

    Meschede, 59872

    Mohammad Wattad

    Recruiting
  • KH Kliniken Maria Hilf

    Mönchengladbach, 41063

    Ulrich Graeven

    Recruiting
  • Krankenhaus Muenchen-Schwabing

    Munich, 80804

    Clemens Wendtner

    Recruiting
  • Klinikum Rechts der Isar - Technische Universitaet Muenchen

    Munich, 81675

    Simon Heidegger

    Recruiting
  • Kliniken Ostalb, Stauferklinikum Schwäbisch Gmünd

    Mutlangen, 73557

    Holger Hebart

    Recruiting
  • Klinikum Oldenburg

    Oldenburg, 26133

    Andrea Renzelmann

    Recruiting
  • Brüderkrankenhaus St. Josef Paderborn

    Paderborn, 33098

    Tobias Gaska

    Recruiting
  • Universitätsklinik Rostock

    Rostock, 18057

    Sebastian Böttcher

    Recruiting
  • Caritas-Klinik St. Theresia

    Saarbrücken, 66113

    Michael Clemens

    Recruiting
  • Klinikum Sindelfingen-Böbingen

    Sindelfingen, 71065

    Markus Ritter

    Recruiting
  • Marienhospital Stuttgart

    Stuttgart, 70199

    Claudio Denzlinger

    Recruiting
  • Universitaetsklinik Tuebingen

    Tübingen, 72076

    Stefan Wirths

    Recruiting
  • Universitätsklinik Ulm

    Ulm, 89081

    Christof Schneider

    Recruiting

Other trials in Germany

About this study

Official title: A Prospective, Open-label, Multicentre, Randomized, Phase-3-trial of Acalabrutinib, Obinutuzumab and Venetoclax (GAVE) Compared to Obinutuzumab and Venetoclax (GVE) in Previously Untreated Patients With High Risk Chronic Lymphocytic Leukemia (CLL)

This multicenter, prospective, open-label, randomized, superiority phase 3 study is designed to demonstrate that treatment with a triple combination of acalabrutinib, obinutuzumab and venetoclax (GAVe) prolong the progression-free survival (PFS) as compared to treatment with the combination of obinutuzumab and venetoclax (GVe) in pa-tients with high risk CLL (defined as having at least one of the follow-ing risk factors: 17p-deletion, TP53-mutation, complex karyotype or an unmutated IGHV-gene status).

Read the detailed description

CLL is the most frequent leukemia in industrialized countries. International guidelines agree on diagnosis and management of this disease. The clinical course of CLL is highly variable and can be predicted by clinical staging (according to Rai and Binet) as well as genetic, serum markers and risk models. This study is designed for a randomized comparison of two different, non-chemotherapeutic and fixed-duration modalities for patients with high risk chronic lymphocytic leukemia (CLL) and addresses a high medical need, since high risk-CLL represents a so far incurable, aggressive cancer. The high risk-group of CLL patients can be identified by molecular characteristics, allowing the inclusion of a clearly described group of patients: 17p-deletion, TP53-mutation and/or complex karyotype.TP53 defects are the strongest prognostic factors for non-response to chemotherapy. Patients harboring TP53 defects should be treated with chemotherapy-free regimens. Complex karyotype (CKT), defined as the presence of three or more chromosomal aberrations in two or more metaphases is associated with a poorer outcome in various hematologic malignancies, including chronic lymphocytic leukemia (CLL). In CLL, CKT is one of several well established adverse prognostic factors, comparable to 17p-deletion, TP53-mutation or unmutated IGHV status. Depending on age and prior exposure to chemotherapy, 10-30% of patients with CLL exhibit CKT. A broad body of evidence has suggested a predictive prognostic value of CKT. Despite considerable advances with chemoimmunotherapy in the treatment of frontline as well as relapsed/refractory (r/r) CLL, outcome of patients with CKT remains poor. To date, a randomized comparison to optimize the treatment of patients with high risk disease defined as either the presence of TP53 aberrations or CKT, by novel agents has not been performed. Patients with high risk CLL (TP53-defects and/or CKT) have a poor outcome with chemoimmunotherapy and do not benefit to the same extent from approved regimen such as continuous treatment of ibrutinib or 12 months treatment with obinutuzumab plus venetoclax. Monotherapy with BTK-inhibitor is less effective in those patients as compared with patients without high risk disease. Venetoclax combined with the anti-CD20 monoclonal antibody obinutuzumab offers a highly effective fixed-duration treatment option with a manageable toxicity profile. The recent results of the CLL14 study define a new standard of a fixed 12-months treatment with obinutuzumab and venetoclax in previously untreated patients yielding a major benefit also for patients with high risk disease as compared to chemoimmunotherapy. However, high risk patients appear to progress earlier than low risk patients and the therapy is not clearly curative so far. Acalabrutinib is a second generation, selective BTK inhibitor which has shown promising overall response rates in patients with relapsed CLL or patients intolerant to ibrutinib. The development of acalabrutinib focussed on minimization of off-target activity. Results of a three-arm study investigating the combination of acalabrutinib plus obinutuzumab versus acalabrutinib alone versus chlorambucil plus obinutuzumab (NCT02475681) showed a substantial improvement of PFS for the combination arm and the monotherapy versus the standard chemoimmunotherapy regimen. The addition of a BTK-inhibitor, such as acalabrutinib to obinutuzumab and venetoclax has the potential to result in a better outcome, because synergistic effects have been reported between BTK inhibitors and B-cell lymphoma 2 (BCL-2) inhibitors or for BCL-2 inhibitors and monoclonal antibodies. Synergistic effects, which are expected to reduce early progressions or insufficient responses, are in particular important for this high risk population. The triple combination of acalabrutinib, obinutuzumab (or rituximab) and venetoclax has been investigated in a phase 1 b- study and had a tolerable safety profile with minimal to no drug-drug interactions, results of a phase 2 trial studying the same combination showed that the triple combination was highly active with 78% undetectable MRD levels in the bone marrow . Currently, the GCLLSG conducts phase 2 studies, investigating a triple combination consisting of BTK- and Bcl2-inhibitors and monoclonal antibodies (CLL2GIVe: NCT02758665; CLL2BAAG: NCT03787264) and a large phase 3 trial with one experimental arm with a triple combination (CLL13, NCT02950051) but results are not yet published. Acalabrutinib, venetoclax and obinutuzumab is now being studied in a registrational phase 3 trial CL-311 (NCT03836261) against the current standard of chemoimmunotherapy (fludarabine/cyclophosphamide/rituximab (FCR), bendamustine/rituximab (BR) in patients without 17p-deletion or TP53-mutation. Acalabrutinib is indicated in Germany as monotherapy or in combination with obinutuzumab for the treatment of adult patients with treatment-naive chronic lymphocytic leukemia (CLL) and as monotherapy for the treatment of adult patients with relapsed chronic lymphocytic leukemia (CLL).

Being tested
Obinutuzumab, Venetoclax, Acalabrutinib
Keywords
CLL, high risk, tp53 aberration, complex karyotype, unmutated IGHV gene status
Medical subject headings
Leukemia, Lymphocytic, Chronic, B-Cell

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • ObinutuzumabDrug

    Also called Gazyva, Gazyvaro

    Obinutuzumab i.v. infusion:

    Cycle 1 Day 1: Obinutuzumab 100 mg i.v.

    Cycle 1 Day 1 (or 2): Obinutuzumab 900 mg i.v.

    Cycle 1 Day 8: Obinutuzumab 1000 mg i.v.

    Cycle 1 Day 15: Obinutuzumab 1000 mg i.v.

    Cycles 2-6: Day 1: Obinutuzumab 1000 mg i.v.

  • VenetoclaxDrug

    Also called Venclexta, Venclyxto

    Venetoclax p.o.:

    Cycle 1: Days 22-28: Venetoclax 20 mg (2 x 10 mg)

    Cycle 2: Days 1-7: Venetoclax 50 mg (1 x 50 mg)

    Cycle 2:Days 8-14: Venetoclax 100 mg (1 x 100 mg)

    Cycle 2:Days: 15-21: Venetoclax 200 mg (2 x 100 mg)

    Cycle 2:Days: 22-28: Venetoclax 400 mg (4 x 100 mg)

    Cycles 3-12: Days 1-28: Venetoclax 400 mg (4 x 100 mg)

  • AcalabrutinibDrug

    Also called Calquence

    Cycles 15-24: Days 1-28:

    100 mg acalabrutinib twice daily p.o. approx. every 12 hrs (corresponding to a total daily dose of 200 mg).

Study groups in NCT05197192
Study groupRoleWhat they receive
GAVe-ArmExperimentalAcalabrutinib plus Venetoclax plus Obinutuzumab plus (GAVe)
Receives: Drug: Obinutuzumab; Drug: Venetoclax; Drug: Acalabrutinib
GVe-ArmExperimentalObinutuzumab plus Venetoclax (GVe)
Receives: Drug: Obinutuzumab; Drug: Venetoclax

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Progression-free survival (PFS)

    The study is designed to demonstrate that 14 cycles of treatment with GAVe followed by up to 10 cycles maintenance with acalabrutinib for patients with detectable MRD at cycle 14 day 14 prolong PFS as compared to 12 cycles of treatment with GVe in patients with high risk CLL (defined as hav-ing at least one of the following risk factors: 17p-deletion, TP53- mutation or complex karyotype).

    Measured: 50 months after FPI

Secondary outcomes (8)
  1. Minimal residual disease (MRD) levels

    Minimal residual disease (MRD) levels in the peripheral blood (PB) and in the bone marrow (BM) at final restaging ((Staging 5) cycle 15 day 1 for patients in GVe study arm, cycle 14 day 14 for patients in GAVe study arm)

    Measured: 50 months after FPI

  2. MRD in PB at cycle 27 day 1

    MRD in PB at cycle 27 day 1 for all patients (end of maintenance for patients in GAVe study arm, who had detectable MRD levels after 14 cycles of GAVe-treatment)

    Measured: 50 months after FPI

  3. Overall response rate

    Overall response rate (ORR; as per iwCLL guidelines) at cycle 15

    Measured: 50 months after FPI

  4. Complete response rate

    Complete response rate (CRR; as per iwCLL guidelines) at cycle 15

    Measured: 50 months after FPI

  5. Overall Survival (OS)

    Overall Survival (OS)

    Measured: 50 months after FPI

  6. Event-free survival (EFS)

    Event-free survival (EFS)

    Measured: 50 months after FPI

  7. Duration of response (DOR)

    Duration of response (DOR)

    Measured: 50 months after FPI

  8. Time to next treatment (TTNT)

    Time to next treatment (TTNT)

    Measured: 50 months after FPI

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Jan 2022
  2. Study start19 Apr 2022
  3. Primary completionMay 2028 (estimated)
  4. Study completionMay 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
202 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05197192
Sponsor's protocol ID
CLL16
Other IDs
2023-506414-46-00, 2023
Status last verified
Aug 2026
First submitted
27 Sep 2021
Last updated
20 Aug 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Obinutuzumab, Venetoclax and Acalabrutinib in people with Chronic Lymphocytic Leukemia, run by German CLL Study Group at 30 sites in Germany.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 10 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 20 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 30 sites in Germany. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Barbara Eichhorst, MD, Prof. (+4922147888220, barbara.eichhorst@uk-koeln.de), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Progression-free survival (PFS) (time frame: 50 months after FPI). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Aug 2026.

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