Obinutuzumab With High-dose Ibrutinib for the Treatment of Patients With Chronic Lymphocytic Leukemia With Progressive Disease on Single Agent Ibrutinib.

• ClinicalTrials.gov Identifier: NCT02611908
• Recruitment Status: Withdrawn
• First Posted: November 23, 2015
• Last Update Posted: January 25, 2019
• Sponsor: Michael Choi
• Collaborator: Pharmacyclics LLC.
• Information provided by (Responsible Party): Michael Choi, University of California, San Diego

Study Description

Brief Summary:

The purpose of the study is to investigate whether the combination of obinutuzumab and ibrutinib (administered up to 840 mg per day) might be useful for the treatment of CLL or SLL that is not responding or no longer responding to treatment with ibrutinib alone. The study will evaluate whether this regimen can reduce the amount of cancerous cells in the body. Subjects will be treated with ibrutinib at a dose of up to 840 mg a day by mouth, as well as obinutuzumab infusions. Although both of these agents are approved by the FDA for the treatment of CLL or SLL, the combination and the dosing schedule of ibrutinib are considered experimental.

Condition or disease	Intervention/treatment	Phase
Chronic Lymphocytic Leukemia	Drug: ibrutinib; Drug: obinutuzumab	Phase 1

Detailed Description:

This is phase 1 study for patients with CLL or small lymphocytic lymphoma (SLL) experiencing disease progression on single ibrutinib. This study will evaluate the optimal ibrutinib dose (including doses higher than 420 mg) when combined with obinutuzumab.

During the screening period, patients will continue on ibrutinib at their previous tolerated dose, unless required to stop (e.g.: by a preceding clinical trial).

On cycle 1, day 1, the dose of ibrutinib will be assigned based on the dose cohort. Patients in cohort 1 will receive ibrutinib 420 mg PO daily. Patients in cohort 2 will receive ibrutinib 560 mg PO daily. Cohort 3 will be 700 mg PO daily. Cohort 4 will be 840 mg PO daily.

On cycle 1, day 1, patients will also initiate treatment with obinutuzumab (100 mg on day 1, 900mg on day 2, 1000mg day 8, 15, 28 then q 28 days for a total of 8 doses).

The primary safety endpoint is determination of DLTs during the first 28 days. The primary efficacy endpoint of overall response rate will be assessed 2 months after the final dose of obinutuzumab.

Study Design

• Study Type: Interventional (Clinical Trial)
• Actual Enrollment: 0 participants
• Intervention Model: Sequential Assignment
• Masking: None (Open Label)
• Primary Purpose: Treatment
• Official Title: A Phase 1 Clinical Trial to Evaluate Obinutuzumab With High-dose Ibrutinib for the Treatment of Patients With Chronic Lymphocytic Leukemia With Progressive Disease on Single Agent Ibrutinib.
• Study Start Date: June 2016
• Estimated Primary Completion Date: November 2019
• Estimated Study Completion Date: November 2020

Arms and Interventions

Arm	Intervention/treatment
Experimental: ibrutinib +obinutuzumab	Drug: ibrutinib; Cohort 1 420 mg PO daily Cohort 2 560 mg PO daily Cohort 3 700 mg PO daily Cohort 4 840 mg PO daily; Other Name: Imbruvica; Drug: obinutuzumab; obinutuzumab 100 mg IV on day 1, 900mg IV on day 2, 1000mg IV day 8, 15, 28 then q 28 days for a total of 8 doses.; Other Name: Gazyva

Outcome Measures

Primary Outcome Measures :

1. Maximum tolerated dose [ Time Frame: 2 months ]

Secondary Outcome Measures :

1. Treatment-emergent adverse events [ Time Frame: 2 years ]
2. overall response rate [ Time Frame: 2 months ]
3. progression free survival [ Time Frame: 2 months ]
4. stable disease rate [ Time Frame: 2 months ]

Eligibility Criteria

• Ages Eligible for Study: 18 Years and older (Adult, Older Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Criteria

Inclusion Criteria:

• Clinical and phenotypic verification of B cell CLL or SLL and measurable disease.
• Prior therapy: Patients must have been receiving single agent ibrutinib therapy at the time of disease progression. Patient may have received other therapy in combination with ibrutinib earlier in the their treatment course. Prior obinutuzumab therapy is also permitted.
• Progressive disease on current single agent ibrutinib therapy (but not within the first 2 months of initiating ibrutinib therapy). Progression is based on 2008 iwCLL definition.
• ECOG performance status of 0-2.
• Adequate hematologic function.
• Adequate renal function.
• Adequate hepatic function.

Exclusion Criteria:

• Known CNS lymphoma or leukemia
• History of Richter's or prolymphocytic transformation.
• Primary ibrutinib resistance, defined by progressive disease within the first 2 months of first initiating ibrutinib therapy.
• Uncontrolled autoimmune hemolytic anemia (AIHA) or idiopathic thrombocytopenia purpura (ITP)

• CLL therapy, with the exception of ibrutinib within the following timeframes:

  1. Chemotherapy, external beam radiation therapy, anticancer antibodies within 30 days prior to the first dose of drug on this study.
  2. Corticosteroid use 20mg prednisone within 1 week prior to first dose on this study.
  3. Radio- or toxin-conjugated antibody therapy within 10 weeks prior to first dose on this study.
  4. Allogeneic stem cell transplant within 6 months prior to first dose on this study
• History of major surgery within 4 weeks prior to first dose on this study.
• History of prior malignancy, with the exception of adequately treated non-melanoma skin cancer, malignancies treated with curative intent and with no evidence of active disease for more than 3 years, or adequately treated cervical carcinoma in situ without current evidence of disease.
• Currently active clinically significant cardiovascular disease or history of myocardial infarction within 6 months of first dose.
• Serologic status and/or PCR testing reflecting active hepatitis B or C infection.
• Known history of infection with human immunodeficiency virus (HIV).
• Unable to swallow capsules or disease significantly affecting gastrointestinal function.
• History of stroke or intracranial hemorrhage within 6 months of first dose.
• Requires anticoagulation with warfarin or other Vitamin K antagonists.
• Requires treatment with a strong CYP 3A inhibitor.
• Pregnant or breast-feeding women
• Women of child-bearing age must obtain a pregnancy test and pregnant or breast feeding females
• Patients who are currently receiving another investigational therapy
• Current infection requiring parenteral antibiotics.

Contacts and Locations

Sponsors and Collaborators

Michael Choi

Pharmacyclics LLC.

Investigators

• Principal Investigator: Michael Choi, MD; University of California, San Diego

More Information

• Responsible Party: Michael Choi, Assistant Clinical Professor, University of California, San Diego
• ClinicalTrials.gov Identifier: NCT02611908
• Other Study ID Numbers: 151231
• First Posted: November 23, 2015
• Last Update Posted: January 25, 2019
• Last Verified: January 2019

• Studies a U.S. FDA-regulated Drug Product: Yes
• Studies a U.S. FDA-regulated Device Product: No

Keywords provided by Michael Choi, University of California, San Diego:

CLL; cancer; obinutuzumab; ibrutinib; SLL

Additional relevant MeSH terms:

Leukemia; Leukemia, Lymphoid; Leukemia, Lymphocytic, Chronic, B-Cell; Disease Progression; Neoplasms by Histologic Type; Neoplasms; Lymphoproliferative Disorders; Lymphatic Diseases; Immunoproliferative Disorders; Immune System Diseases; Leukemia, B-Cell; Chronic Disease; Disease Attributes; Pathologic Processes; Obinutuzumab; Antineoplastic Agents, Immunological; Antineoplastic Agents