A Study of Acalabrutinib vs Investigator's Choice of Idelalisib Plus Rituximab or Bendamustine Plus Rituximab in R/R CLL

Chronic Lymphocytic Leukemia Clinical Trial

Official title:

A Randomized, Multicenter, Open-Label, Phase 3 Study of Acalabrutinib (ACP-196) Versus Investigator's Choice of Either Idelalisib Plus Rituximab or Bendamustine Plus Rituximab in Subjects With R/R Chronic Lymphocytic Leukemia

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT02970318
• Other study ID #: ACE-CL-309
• Secondary ID: 2015-004454-17
• Status: Active, not recruiting
• Phase: Phase 3
• Start date: February 2, 2017
• Est. completion date: September 6, 2027

Study information

• Verified date: May 2024
• Source: Acerta Pharma BV
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study is designed to evaluate the efficacy of acalabrutinib compared with rituximab in combination with idelalisib or bendamustine in previously treated subjects with chronic lymphocytic leukemia (CLL).

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 310
• Est. completion date: September 6, 2027
• Est. primary completion date: September 3, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

1. Men and women = 18 years of age.

2. ECOG performance status of 0 to 2.

3. Diagnosis of CLL that meets published diagnostic criteria (Hallek 2008):

1. Monoclonal B-cells (either kappa or lambda light chain restricted) that are clonally co-expressing = 1 B-cell marker (CD19, CD20, or CD23) and CD5.

2. Prolymphocytes may comprise = 55% of blood lymphocytes.

3. Presence of = 5 x 10^9 B lymphocytes/L (5000/µL) in the peripheral blood (at any point since initial diagnosis).

4. Must have documented CD20-positive CLL.

5. Active disease meeting = 1 of the following IWCLL 2008 criteria for requiring treatment:

1. Evidence of progressive marrow failure as manifested by the development of, or worsening of, anemia (hemoglobin < 10 g/dL) and/or thrombocytopenia (platelets < 100,000/µL).

2. Massive (i.e., = 6 cm below the left costal margin), progressive, or symptomatic splenomegaly.

3. Massive nodes (i.e., = 10 cm in the longest diameter), progressive, or symptomatic lymphadenopathy.

4. Progressive lymphocytosis with an increase of > 50% over a 2-month period or a LDT of < 6 months. LDT may be obtained by linear regression extrapolation of ALC obtained at intervals of 2 weeks over an observation period of 2 to 3 months. In subjects with initial blood lymphocyte counts of < 30 x 10^9/L (30,000/µL), LDT should not be used as a single parameter to define indication for treatment. In addition, factors contributing to lymphocytosis or lymphadenopathy other than CLL (e.g., infections) should be excluded.

5. Autoimmune anemia and/or thrombocytopenia that is poorly responsive to standard therapy.

6. Constitutional symptoms documented in the subject's chart with supportive objective measures, as appropriate, defined as = 1 of the following disease-related symptoms or signs:

i. Unintentional weight loss = 10% within the previous 6 months before screening.

ii. Significant fatigue (ECOG performance score 2; inability to work or perform usual activities).

iii. Fevers higher than 100.5°F or 38.0°C for = 2 weeks before screening without evidence of infection.

iv. Night sweats for > 1 month before screening without evidence of infection.

6. Meet the following laboratory parameters:

1. ANC = 750 cells/µL (0.75 x 10^9/L), or = 500 cells/µL (0.50 x 10^9/L) in subjects with documented bone marrow involvement, and independent of growth factor support 7 days before assessment.

2. Platelet count = 50,000 cells/µL (50 x 10^9/L), or = 30,000 cells/µL (30 x 10^9/L) in subjects with documented bone marrow involvement, and without transfusion support 7 days before assessment. Subjects with transfusion-dependent thrombocytopenia are excluded. If an Investigator has chosen bendamustine/rituximab as the Arm B treatment, platelets must be = 75,000 cells/µL (75 x 10^9/L).

3. Serum AST and ALT = 2.0 x ULN.

4. Total bilirubin = 1.5 x ULN.

5. Estimated creatinine clearance of = 30 mL/min, calculated using the formula of Cockcroft and Gault [(140-Age) • Mass (kg)/(72 • creatinine mg/dL); multiply by 0.85 if female].

7. Must have received = 1 prior systemic therapies for CLL. Note: Single-agent steroids or localized radiation are not considered a prior line of therapy. If a single-agent anti-CD20 antibody was previously administered, subjects must have received = 2 doses.

8. Women who are sexually active and can bear children must agree to use highly effective forms of contraception while on the study and for 2 days after the last dose of acalabrutinib, 90 days after the last dose of idelalisib, 6 months after the last dose of bendamustine, or 12 months after the last dose of rituximab, whichever is longer. Highly effective forms of contraception are defined in Section 9.2.5.

9. Men who are sexually active and can beget children must agree to use highly effective forms of contraception during the study and for 90 days after the last dose of idelalisib, 6 months after the last dose of bendamustine, or 12 months after the last dose of rituximab, whichever is longer. Highly effective forms of contraception are defined in Section 9.2.5.

10. Men must agree to refrain from sperm donation during the study and for 90 days after the last dose of idelalisib, 6 months after the last dose of bendamustine, or 12 months after the last dose of rituximab, whichever is longer.

11. Willing and able to participate in all required evaluations and procedures in this study protocol, including swallowing capsules without difficulty.

12. Ability to understand the purpose and risks of the study and provide signed and dated informed consent and authorization to use protected health information (in accordance with national and local patient privacy regulations).

Exclusion Criteria:

1. Known CNS lymphoma or leukemia.

2. Known prolymphocytic leukemia or history of, or currently suspected, Richter's syndrome.

3. Uncontrolled AIHA or ITP defined as declining hemoglobin or platelet count secondary to autoimmune destruction within the screening period or requirement for high doses of steroids (> 20 mg daily of prednisone or equivalent).

4. Prior exposure to a BCL-2 inhibitor (e.g., venetoclax/ABT-199) or a BCR inhibitor (e.g., BTK inhibitors or PI3K inhibitors). Prior bendamustine is allowed if Investigator's choice for treatment in Arm B is idelalisib with rituximab. Bendamustine retreatment is allowed if the prior response to bendamustine lasted > 24 months.

5. Received any chemotherapy, external beam radiation therapy, anticancer antibodies, or investigational drug within 30 days before first dose of study drug.

6. Corticosteroid use > 20 mg daily prednisone equivalent within 1 week before first dose of study drug, except as indicated for other medical conditions such as inhaled steroid for asthma, topical steroid use, or as premedication for administration of study drug or contrast. For example, subjects requiring steroids at daily doses > 20 mg prednisone equivalent systemic exposure daily, or those who are administered steroids for leukemia control or white blood cell count lowering are excluded.

7. Prior radio- or toxin-conjugated antibody therapy.

8. Prior allogeneic stem cell transplant or prior autologous transplant within 6 months of first dose of study drug(s) or presence of graft-vs-host disease or receiving treatment for graft-vs-host disease.

9. Major surgical procedure within 30 days of first dose of study drug. Note: If a subject had major surgery, they must have recovered adequately from any toxicity and/or complications from the intervention before the first dose of study drug.

10. History of prior malignancy except for the following:

1. Malignancy treated with curative intent and with no evidence of active disease present for more than 2 years before screening and felt to be at low risk for recurrence by treating physician.

2. Adequately treated lentigo maligna melanoma without current evidence of disease or adequately controlled nonmelanomatous skin cancer.

3. Adequately treated carcinoma in situ without current evidence of disease.

11. Significant cardiovascular disease such as uncontrolled or untreated 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 QTc > 480 msec (calculated using Fridericia's formula: QT/RR^0.33) at screening. Exception: Subjects with controlled, asymptomatic atrial fibrillation during screening are allowed to enroll on study.

12. 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.

13. Received a live virus vaccination within 28 days of first dose of study drug.

14. Known history of infection with HIV or any uncontrolled active systemic infection (e.g., bacterial, viral, or fungal). For study sites in Germany: active infection with human immunodeficiency virus (seropositivity for HIV-1 or HIV-2 antibodies, and if positive, reactivity against the HIV-specific p24 antigen).

15. Active CMV infection (active viremia as evidenced by positive polymerase chain reaction [PCR] result for CMV DNA).

16. Serologic status reflecting active hepatitis B or C infection.

1. Subjects who are anti-HBc positive and who are surface antigen negative will need to have a negative PCR result before randomization. Those who are HbsAg-positive or hepatitis B PCR positive will be excluded.

2. Subjects who are hepatitis C antibody positive will need to have a negative PCR result before randomization. Those who are hepatitis C PCR positive will be excluded.

17. Ongoing, drug-induced liver injury, alcoholic liver disease, non-alcoholic steatohepatitis, primary biliary cirrhosis, ongoing extrahepatic obstruction caused by cholelithiasis, cirrhosis of the liver, or portal hypertension.

18. History of or ongoing drug-induced pneumonitis.

19. History of serious allergic reactions including anaphylaxis and toxic epidermal necrolysis.

20. History of stroke or intracranial hemorrhage within 6 months before first dose of study drug.

21. History of bleeding diathesis (e.g., hemophilia, von Willebrand disease).

22. Requires or receiving anticoagulation with warfarin or equivalent vitamin K antagonists (e.g., phenprocoumon) within 7 days of first dose of study drug.

23. Presence of a gastrointestinal ulcer diagnosed by endoscopy within 3 months before screening.

24. Requires treatment with a strong CYP3A inhibitor/inducer.

25. Requires treatment with proton-pump inhibitors (e.g., omeprazole, esomeprazole, lansoprazole, dexlansoprazole, rabeprazole, or pantoprazole). Subjects receiving proton-pump inhibitors who switch to H2-receptor antagonists or antacids are eligible for enrollment to this study.

26. Breast feeding or pregnant.

27. Concurrent participation in another therapeutic clinical trial.

28. Prothrombin time/INR or aPTT (in the absence of a Lupus anticoagulant) > 2.0 x ULN. Exception: Subjects receiving warfarin are excluded, however, those receiving other anticoagulant therapy who have a higher INR/aPTT may be permitted to enroll to this study after discussion with the medical monitor.

29. History of confirmed progressive multifocal leukoencephalopathy (PML)

Related Conditions & MeSH terms

• Chronic Lymphocytic Leukemia
• Leukemia
• Leukemia, Lymphocytic, Chronic, B-Cell
• Leukemia, Lymphoid

Intervention

Drug:
• Acalabrutinib (ACP-196)
Acalabrutinib monotherapy
• Rituximab
Rituximab in combination with idelalisib or bendamustine
• Idelalisib
Idelalisib in combination with rituximab
• Bendamustine
Bendamustine in combination with rituximab

Locations

Country	Name	City	State
Australia	Research Site	Adelaide
Australia	Research Site	Box Hill
Australia	Research Site	Frankston
Australia	Research Site	Geelong
Australia	Research Site	Gosford
Australia	Research Site	Hobart
Australia	Research Site	Kogarah
Australia	Research Site	Murdoch
Australia	Research Site	Nedlands
Australia	Research Site	South Brisbane
Australia	Research Site	Woodville
Austria	Research Site	Linz
Austria	Research Site	Salzburg
Austria	Research Site	Wels
Austria	Research Site	Wien
Austria	Research Site	Wien
Belgium	Research Site	Antwerpen
Belgium	Research Site	Ghent
Belgium	Research Site	Roeselare
Belgium	Research Site	Yvoir
Bulgaria	Research Site	Pleven
Bulgaria	Research Site	Plovdiv
Bulgaria	Research Site	Stara Zagora
Bulgaria	Research Site	Vratsa
Canada	Research Site	Barrie	Ontario
Canada	Research Site	Calgary
Canada	Research Site	Montreal
Canada	Research Site	Ottawa
Canada	Research Site	Regina
Canada	Research Site	Saint John
Canada	Research Site	Toronto
Canada	Research Site	Toronto
Croatia	Research Site	Zadar
Croatia	Research Site	Zagreb
Czechia	Research Site	Brno
Czechia	Research Site	Novy Hradec Kralove
Czechia	Research Site	Olomouc
Czechia	Research Site	Ostrava Poruba
Czechia	Research Site	Plzen - Lochotin
Czechia	Research Site	Praha 10
France	Research Site	Bordeaux
France	Research Site	Brest
France	Research Site	Montpellier
France	Research Site	Nantes cedex 1
France	Research Site	Paris
France	Research Site	Paris cedex 13
France	Research Site	Perpignan
France	Research Site	Provence Alpes Cote D'Azur
France	Research Site	Rennes Cedex
France	Research Site	Rouen
Germany	Research Site	Aschaffenburg
Germany	Research Site	Dresden
Germany	Research Site	Munchen
Germany	Research Site	Mutlangen
Germany	Research Site	Ulm
Hong Kong	Research Site	HongKong
Hong Kong	Research Site	Pok Fu Lam
Hungary	Research Site	Budapest
Hungary	Research Site	Debrecen
Hungary	Research Site	Gyula
Hungary	Research Site	Kaposvár
Israel	Research Site	Ashkelon
Israel	Research Site	Haifa
Israel	Research Site	Jerusalem
Israel	Research Site	Kfar Saba
Israel	Research Site	Nahariya
Israel	Research Site	Petah Tikvah
Italy	Research Site	Aviano
Italy	Research Site	Bergamo
Italy	Research Site	Brescia
Italy	Research Site	Firenze
Italy	Research Site	Genova
Italy	Research Site	Genova
Italy	Research Site	Meldola
Italy	Research Site	Milan
Italy	Research Site	Milano
Italy	Research Site	Modena
Korea, Republic of	Research Site	Busan
Korea, Republic of	Research Site	Daegu
Korea, Republic of	Research Site	Dong-gu
Korea, Republic of	Research Site	Gyeonggi-do
Korea, Republic of	Research Site	Incheon
Korea, Republic of	Research Site	Jeonju-si
Korea, Republic of	Research Site	Seoul
Korea, Republic of	Research Site	Seoul
New Zealand	Research Site	Addington
New Zealand	Research Site	Dunedin
New Zealand	Research Site	Palmerston North
New Zealand	Research Site	Tauranga
Poland	Research Site	Bialystok
Poland	Research Site	Bydgoszcz
Poland	Research Site	Gdansk
Poland	Research Site	Kraków
Poland	Research Site	Lodz
Poland	Research Site	Lublin
Poland	Research Site	Woj. Podkarpackie
Russian Federation	Research Site	Novosibirsk
Russian Federation	Research Site	Obninsk
Russian Federation	Research Site	Penza
Russian Federation	Research Site	Ryazan
Russian Federation	Research Site	Sochi
Russian Federation	Research Site	St. Petersburg
Russian Federation	Research Site	St. Petersburg
Russian Federation	Research Site	Tula
Russian Federation	Research Site	Volgograd
Russian Federation	Research Site	Yaroslavl
Russian Federation	Research Site	Yekaterinburg
Singapore	Research Site	SGP
Singapore	Research Site	SGP
Singapore	Research Site	SGP
Slovakia	Research Site	Bratislava
Slovakia	Research Site	Kosice
Spain	Research Site	Badalona
Spain	Research Site	Madrid
Spain	Research Site	Madrid
Spain	Research Site	Madrid
Spain	Research Site	Madrid
Spain	Research Site	Madrid
Spain	Research Site	Majadahonda
Spain	Research Site	Salamanca
Spain	Research Site	Santander
Spain	Research Site	Valencia
Sweden	Research Site	Goeteborg
Sweden	Research Site	Lulea
Sweden	Research Site	Stockholm
Taiwan	Research Site	Hualien
Taiwan	Research Site	Tainan
Taiwan	Research Site	Taipei
Ukraine	Research Site	Cherkasy
Ukraine	Research Site	Dnipropetrovsk
Ukraine	Research Site	Ivano-Frankivsk
Ukraine	Research Site	Khmelnytsky
Ukraine	Research Site	Kyiv
Ukraine	Research Site	Kyiv
Ukraine	Research Site	Zhytomir
United Kingdom	Research Site	Birmingham
United Kingdom	Research Site	Cambridge
United Kingdom	Research Site	Canterbury
United Kingdom	Research Site	Leicester
United Kingdom	Research Site	London
United Kingdom	Research Site	Maidstone
United Kingdom	Research Site	Manchester
United Kingdom	Research Site	Southampton
United Kingdom	Research Site	Wolverhampton
United States	Research Site	Athens	Georgia
United States	Research Site	Brick	New Jersey
United States	Research Site	Canton	Ohio
United States	Research Site	Cedar Rapids	Iowa
United States	Research Site	Chandler	Arizona
United States	Research Site	Fort Sam Houston	Texas
United States	Research Site	Joliet	Illinois
United States	Research Site	Lincoln	Nebraska
United States	Research Site	Mount Sterling	Kentucky
United States	Research Site	Nyack	New York
United States	Research Site	Oxnard	California
United States	Research Site	Round Rock	Texas
United States	Research Site	Saint Cloud	Minnesota

Sponsors (1)

Lead Sponsor	Collaborator
Acerta Pharma BV

Countries where clinical trial is conducted

United States,  Australia,  Austria,  Belgium,  Bulgaria,  Canada,  Croatia,  Czechia,  France,  Germany,  Hong Kong,  Hungary,  Israel,  Italy,  Korea, Republic of,  New Zealand,  Poland,  Russian Federation,  Singapore,  Slovakia,  Spain,  Sweden,  Taiwan,  Ukraine,  United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Progression-free Survival (PFS) Per Independent Review Committee (IRC) Assessment	To evaluate the efficacy of acalabrutinib monotherapy (Arm A) compared with idelalisib/rituximab or bendamustine/rituximab (Arm B) based on Independent Review Committee (IRC) assessment of progression-free survival (PFS) per International Workshop on Chronic Lymphocytic Leukemia (IWCLL) 2008 criteria (Hallek 2008) with incorporation of the clarification for treatment-related lymphocytosis (Cheson 2012) hereafter referred to as IWCLL 2008 criteria in subjects with relapsed or refractory (R/R) chronic lymphocytic leukemia (CLL). As planned and reported in the interim clinical study report (dated 17 July 2019), because the study did cross the boundary at interim analysis.; IRC assessments were discontinued after the interim analysis. All IRC-related efficacy analyses in this clinical study report were based on the interim analysis data cutoff date of 15 January 2019. All other efficacy analyses were based on the final analysis data cutoff date of 03 September 2021.	IRC assessments from randomization date until disease progression or death or IRC discontinuation on 15Jan2019 (as IA per this data cutoff showed crossing superiority boundary) whichever came first, up to 22 months of follow-up
Secondary	Progression-free Survival (PFS) Per Investigator Assessment	PFS per investigator assessment based on the final analysis data cutoff date of 03 September 2021.	From randomization date to date of disease progression or death due to any cause or data cutoff date on 03Sep2021, whichever came first, regardless of use of subsequent anticancer therapy, until 53 months of follow-up.
Secondary	IRC-assessed Overall Response Rate (ORR) Per IWCLL 2008 Criteria Based on Data Cutoff 15 January 2019 From Interim Analysis	IRC-assessed overall response rate (ORR) including complete response (CR), CR with incomplete blood count recovery (CRi) nodular PR (nPR), and Partial Response (PR)	IRC assessments from randomization date until disease progression or death or IRC discontinuation on 15Jan2019 (as IA per this data cutoff showed crossing superiority boundary) whichever came first, up to 22 months of follow-up
Secondary	Investigator Assessed Overall Response Rate (ORR) Per IWCLL 2008 Criteria Based on Data Cutoff 03 September 2021	IRC-assessed overall response rate (ORR) including complete response (CR), CR with incomplete blood count recovery (CRi) nodular PR (nPR), and Partial Response (PR)	Investigator assessments were done from randomization date until date of death or date of exit from study or data cut off date on 03Sep2021, whichever came first, up to 53 months of follow-up.
Secondary	Overall Survival (OS)	Overall Survival (OS) was based on data cutoff date of 03Sep2021	From randomization date to date of death due to any cause, or date of study discontinuation, or date of data cutoff on 03Sep2021, whichever came first until 54 months of follow-up.
Secondary	Duration of Response (DOR) Per Independent Review Committee (IRC) Assessment Based on 15 January 2019 Data Cutoff From Interim Analysis.	Duration of Response (DOR) is defined as from the first documentation of CR, CRi, PR, or nPR to the earlier of the first documentation of disease progression or death from any cause.	IRC assessments from randomization date until disease progression or death or IRC discontinuation on 15Jan2019 (as IA per this data cutoff showed crossing superiority boundary) whichever came first, up to 22 months of follow-up
Secondary	Duration of Response (DOR) Per Investigator Assessment Based on 03 September 2021 Data Cutoff	Duration of Response (DOR) is defined as from the first documentation of CR, CRi, PR, or nPR to the earlier of the first documentation of disease progression or death from any cause.	Investigator assessments were done from randomization date until date of death or study discontinuation or data cutoff date on 03Sep2021, whichever came first up to 53 months of follow-up.
Secondary	Time to Next Treatment (TTNT) Based on 03 September 2021 Data Cutoff	Time to Next Treatment (TTNT) is defined as the time from date of randomization to date of institution of non-protocol-specified treatment for CLL (or first dose date of acalabrutinib for Arm B subjects crossing over to receive acalabrutinib) or death due to any cause, whichever comes first.	From randomization date to start of non-protocol specified subsequent anticancer therapy for CLL or death due to any cause or study discontinuation or data cutoff date on 03Sep2021,, whichever came first up to 53 months of follow-up.

External Links

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