Study Assessing the Safety and Efficacy of ABT-263 in Subjects With B-cell Chronic Lymphocytic Leukemia (CLL) Who Have Failed at Least One Prior Fludarabine-containing Regimen

A Phase 2b Monotherapy Study of ABT-263 in Subjects With Relapsed or Refractory B-Cell Chronic Lymphocytic Leukemia

This is a Phase 2b, open-label, multicenter, global study assessing the safety and efficacy of ABT-263 in subjects with B-cell CLL who have failed at least one prior fludarabine-containing regimen.

Study Overview

• Status: Withdrawn
• Conditions: B-cell Chronic Lymphocytic Leukemia
• Intervention / Treatment: Drug: ABT-263

• Study Type: Interventional
• Enrollment (Anticipated): 150
• Phase: Phase 2

Participation Criteria

Eligibility Criteria

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

Description

Inclusion Criteria:

• >= 18 yrs of age, have B-cell CLL, failed at least 1 prior fludarabine-containing regimen.
• Refractory to 1 fludarabine-containing regimen is defined as failure to achieve at least PR to the last fludarabine-containing regimen received, or disease progression while receiving the last fludarabine-containing regimen, or disease progression in responders (i.e., achieved a PR or CR) within 6 mos of the last cycle of the last fludarabine-containing regimen received (e.g., fludarabine monotherapy, FR, or FC) or in responders (i.e., achieved a PR or CR ) within 24 mos of the last cycle of FCR.
• Intolerant to fludarabine is defined as discontinuation of therapy within 2 cycles due to side effects/toxicity from the last fludarabine-containing regimen.
• ECOG score of <=1.

• Adequate coagulation, renal, & hepatic function at Screening as follows:

  • Serum creatinine <= 2.0 mg/dL or calculated creatinine clearance >= 50 mL/min;
  • AST & ALT <= 3.0 x ULN;
  • Bilirubin <= 1.5 x ULN.
• Gilbert's Syndrome may have a Bilirubin > 1.5 x ULN; aPTT, PT, not to exceed 1.2 x ULN.

• Adequate bone marrow (BM) independent of any growth factor support (with the exception of subjects with BM heavily infiltrated with underlying disease [80% or more] who may use growth factor support to achieve adequate BM) at Screening as follows:

  • ANC >= 1000/µL;
  • Platelets >= 75,000/mm3 (entry platelet count must be independent of transfusion within 14 days of Screening);
  • Hemoglobin >= 9.0 g/dL.

• History of autologous BM transplant must be > 6 mos post transplant (prior to the 1st dose of study drug) & have adequate BM independent of any growth factor support (with the exception of subjects with BM that is heavily infiltrated with underlying disease [80% or more] who may use growth factor support to achieve adequate BM) at Screening as follows:

  • ANC >= 1500/µL;
  • Platelets >= 125,000/mm3;
  • Hemoglobin >= 10.0 g/dL.
• Female subjects must be surgically sterile, postmenopausal (at least 1 year), or have negative results on a pregnancy test.
• All female subjects not surgically sterile or postmenopausal (at least 1 year) & non-vasectomized male subjects must practice birth control.

Exclusion Criteria:

• History/clinically suspicious for cancer-related CNS disease.
• Undergone allogeneic stem cell transplant.
• Undergone autologous stem cell transplant w/i 6 mos prior to 1st dose.
• History/predisposing condition of bleeding or currently exhibits signs of bleeding.
• Recent history of non-chemotherapy induced thrombocytopenic associated bleeding w/i 6 mos prior to 1st dose.
• Active peptic ulcer disease or other hemorrhagic esophagitis/gastritis.
• Active immune thrombocytopenic purpura or history of being refractory to platelet transfusions w/i 1 yr prior to 1st dose.
• Currently receiving/requires anticoagulation therapy or any drugs or herbal supplements that affect platelet function, with the exception of low-dose anticoagulation medications used to maintain the patency of a central IV catheter.
• Significant history of cardiovascular disease, renal, neurologic, psychiatric, endocrinologic, metabolic, immunologic, or hepatic disease.
• Positive for HIV, Hepatitis B, or Hepatitis C.

• Previous or current malignancies w/i the last 3 yrs:

  • except adequately treated in situ carcinoma of the cervix uteri;
  • basal or squamous cell carcinoma;
  • in situ carcinoma of the bladder;
  • or previous malignancy confined and surgically resected with curative intent.
• Has Prolymphocytic leukemia or Richter's transformation to an aggressive B-cell malignancy.
• Exhibits evidence of other clinically significant uncontrolled condition(s) including, but not limited to uncontrolled systemic infection or diagnosis of fever and neutropenia w/i 1 week prior to study drug.
• Prior exposure to ABT-263.
• Received antibody therapy w/i 30 days prior to 1st dose.
• Received any anti-cancer therapy including chemotherapy, immunotherapy, radiotherapy, hormonal, or any investigational therapy w/i 14 days prior to the 1st dose, or has not recovered to <Gr2 clinically significant AE(s) /toxicity(s) of the previous therapy.
• Received steroid therapy for anti-neoplastic intent, w/i 7 days prior to the 1st dose with the exception of inhaled steroids for asthma, topical steroids, or replacement/stress corticosteroids.
• Received aspirin w/i 7 days prior to the 1st dose.
• Consumed grapefruit or grapefruit products w/i 3 days prior to 1st dose.
• Females pregnant or breast-feeding.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Non-Randomized
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: 1	Drug: ABT-263; Continuous dosing until disease progression using one of the following formulations: 25 mg/mL oral solution OR 50 mg/mL oral solution OR 2.0 grams/bottle powder for oral solution of 25 mg/mL when mixed OR 2.0 grams/bottle powder for oral solution of 50 mg/mL when mixed

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Assess the safety of ABT-263 by evaluating study drug exposure, adverse events, serious adverse events, all deaths, as well as changes in laboratory determinations and vital sign parameters.	monthly (at a minimum)
Assess the objective response rate (partial response [PR] and confirmed complete response [CR]) of B-cell CLL subjects treated with ABT-263.	Every 3 months

Secondary Outcome Measures

Outcome Measure	Time Frame
Assess the effects of ABT-263 on duration of overall response, PFS and overall survival in subjects with B-cell CLL.	Every 3 months
Assess the effects of ABT-263 on time to response, 12-month survival rate, time to disease progression (TTP), and disease control rate in subjects with B-cell CLL .	Every 3 months
Investigate the effects of ABT-263 on quality of life (FACT-Leu and EQ-5D), ECOG performance status, and biomarkers in subject with B-cell CLL.	Every 3 months

Collaborators and Investigators

• Sponsor: Abbott
• Collaborators: Genentech, Inc.

Study record dates

Study Major Dates

• Study Start: March 1, 2010
• Primary Completion (Anticipated): December 1, 2012

Study Registration Dates

• First Submitted: May 22, 2009
• First Submitted That Met QC Criteria: June 10, 2009
• First Posted (Estimate): June 11, 2009

Study Record Updates

• Last Update Posted (Estimate): February 26, 2010
• Last Update Submitted That Met QC Criteria: February 25, 2010
• Last Verified: February 1, 2010

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Immune System Diseases; Neoplasms by Histologic Type; Neoplasms; Lymphoproliferative Disorders; Lymphatic Diseases; Immunoproliferative Disorders; Leukemia, B-Cell; Leukemia; Leukemia, Lymphocytic, Chronic, B-Cell; Leukemia, Lymphoid; Antineoplastic Agents; Navitoclax
• Other Study ID Numbers: M10-738