Lenalidomide and Obinutuzumab for Previously Untreated CLL

Sponsor

University of California, San Diego (Other)

Overall Status

Withdrawn

CT.gov ID

NCT02371590

Collaborator

Celgene Corporation (Industry), Genentech, Inc. (Industry)

Enrollment

Location

Arm

Anticipated Duration (Months)

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This is phase 1/2 study for patients with CLL or (SLL) who have not been previously treated. This study will evaluate whether obinutuzumab and lenalidomide is safe and tolerable in this setting and induce complete clinical responses.

Condition or Disease	Intervention/Treatment	Phase
Chronic Lymphocytic Leukemia	Drug: Lenalidomide Drug: Obinutuzumab	Phase 2

Detailed Description

This is phase 1/2 study for patients with CLL or (SLL) who have not been previously treated. The primary endpoint is to determine safety and tolerability of the regimen and determine complete response (CR) to therapy. The secondary endpoints will assess the impact of treatment on progression free and overall survival

Eligible patients will receive obinutuzumab for 6 x 28 day cycles. Patients will also receive lenalidomide orally once daily on days 8-28 of each 28 day cycles. The starting dose for all patients is 5 mg PO daily. At the start of each cycle, there is intra-patient dose-escalation to a maximum of 25mg daily, as tolerated.

Study Design

Study Type:

Interventional

Actual Enrollment :

0 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

A Phase 2 Clinical Trial To Evaluate Lenalidomide And Obinutuzumab For The Treatment Of Patients With Not Previously Treated Chronic Lymphocytic Leukemia

Anticipated Study Start Date :

Feb 1, 2018

Anticipated Primary Completion Date :

Dec 1, 2019

Anticipated Study Completion Date :

Dec 1, 2022

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Lenalidomide-Obinutuzumab All patients receive the combination of lenalidomide and obinutuzumab. There is no randomization or comparator arm.	Drug: Lenalidomide Lenalidomide is administered orally once daily on Days 8-28 of each 28 day cycle. The starting dose for all patients is 5 mg PO daily. At the start of each cycle, there is intra-patient dose-escalation to a maximum of 25mg daily, as tolerated. The study consists of a 6 month treatment period with obinutuzumab and lenalidomide, and an indefinite period of treatment with lenalidomide for as long as it is helpful and tolerated by subject. Other Names: Revlimid Drug: Obinutuzumab Obinutuzumab is administered as follows: Cycle 1: 100mg IV on day 1, 900 mg IV on day 2, 1000mg day 8, 1000 mg on day 15. Cycles 2-6: 1000mg IV on day 1. Other Names: Gazyva

Arm

Intervention/Treatment

Experimental: Lenalidomide-Obinutuzumab

All patients receive the combination of lenalidomide and obinutuzumab. There is no randomization or comparator arm.

Drug: Lenalidomide

Lenalidomide is administered orally once daily on Days 8-28 of each 28 day cycle. The starting dose for all patients is 5 mg PO daily. At the start of each cycle, there is intra-patient dose-escalation to a maximum of 25mg daily, as tolerated. The study consists of a 6 month treatment period with obinutuzumab and lenalidomide, and an indefinite period of treatment with lenalidomide for as long as it is helpful and tolerated by subject.

Other Names:

Revlimid

Drug: Obinutuzumab

Obinutuzumab is administered as follows: Cycle 1: 100mg IV on day 1, 900 mg IV on day 2, 1000mg day 8, 1000 mg on day 15. Cycles 2-6: 1000mg IV on day 1.

Other Names:

Gazyva

Outcome Measures

Primary Outcome Measures

The incidence of dose limiting toxicity [1 year]
For phase 1 portion of study
Complete Response Rate [2 years]
For phase 2 portion of study: iwCLL 2008 defined complete response rate

Secondary Outcome Measures

Number of patients with adverse events associated with lenalidomide-obinutuzumab [2 years]
Progression free survival rate [2 years]
Progression free survival rate at completion of combination therapy, total progression free survival, and overall survival determined by International Working Group in CLL (iwCLL) criteria
Overall response rate [2 years]
Overall response rate (Complete response + partial response) and stable disease rate (also based on 2008 iwCLL guidelines), also at the time of primary endpoint response assessment.

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Main Inclusion Criteria:

Clinical and phenotypic verification of B cell CLL or SLL and measurable disease.
Prior therapy: no prior CLL therapy.
Patients must have progressive disease based on 2008 iwCLL definition with one of the following:

Symptomatic or progressive splenomegaly
Symptomatic lymph nodes, nodal clusters, or progressive lymphadenopathy
Progressive anemia (hemoglobin ≤ 11 g/dL)
Progressive thrombocytopenia (platelets ≤ 100 x 109/L)
Weight loss > 10% body weight over the preceding 6 month period
Fatigue attributable to CLL
Fever or night sweats for > 2 weeks without evidence of infection
Progressive lymphocytosis with an increase of > 50% over a 2-month period or an anticipated doubling time of less than 6 months.
Able to take aspirin (81mg or 325mg) daily, warfarin, low molecular weight heparin, or equivalent anticoagulation as prophylactic medication.
All study participants must be registered into the mandatory Revlimid REMS program, and be willing and able to comply with the requirements of REMS.
Females of childbearing potential (FCBP) must have a negative serum or urine pregnancy test with a sensitivity of at least 50 mIU/mL within 10 - 14 days prior to and again within 24 hours prior to starting Revlimid and must either commit to continued abstinence from heterosexual intercourse or begin TWO acceptable methods of birth control.
Females of reproductive potential must adhere to the scheduled pregnancy testing as required in the Revlimid REMS program.
ECOG performance status of 0-2.
Adequate hematologic function
Adequate renal function
Adequate hepatic function

Exclusion Criteria:

Pregnant or breast-feeding women will not be entered on this study due to risks of fetal and teratogenic adverse events as seen in animal/human studies. Women for child-bearing age must obtain a pregnancy test and pregnant or breast feeding females are excluded.
Known hypersensitivity to thalidomide or lenalidomide (if applicable), including development of erythema nodosum or a desquamating rash while taking thalidomide or similar drugs.
Deep vein thrombosis or superficial thrombophlebitis of any cause on current anticoagulation therapy at the time of screening.
Patients who are currently receiving another investigational agent are excluded.
Current infection requiring parenteral antibiotics.
Known seropositive for or active viral infection with human immunodeficiency virus (HIV); or known active infection with hepatitis B virus (HBV) or hepatitis C virus (HCV) based on detectable viral load. Patients who are seropositive because of hepatitis B virus vaccine or passive immunization by intravenous immunoglobulin (IVIG) are eligible.
Active malignancy within the previous 2 years (other than completely resected non-melanoma skin cancer or carcinoma in situ).
Known central nervous system (CNS) involvement by malignancy.
Untreated autoimmunity such as autoimmune hemolytic anemia, or immune thrombocytopenia.
Insufficient recovery from surgical-related trauma or wound healing.
Impaired cardiac function