Study of Tabalumab (LY2127399) in Japanese Participants With Relapsed or Refactory Multiple Myeloma

• Status: Completed
• Trial end date: 2015-08-01
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this study is to evaluate the safety and effect on the body of Tabalumab (LY2127399) in combination with bortezomib and dexamethasone in Japanese participants with relapsed or refractory multiple myeloma (MM).

• Phase: Phase 1
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Eli Lilly and Company
• Treatments: Antibodies, Monoclonal; BB 1101; Bortezomib; Dexamethasone; Dexamethasone 21-phosphate; Dexamethasone acetate

Criteria

Inclusion Criteria:

• Have relapsed or refractory MM treated with at least 1 prior regimen. Prior therapy with bortezomib is allowed if there was previously at least a minimal response (MR).

• Have measurable disease as defined by one or more of the following:

• serum M-protein concentration ≥ 1 g/dL (10 g/L)

• urine monoclonal light chain concentration ≥ 200 mg/24 hours as determined by urine protein electrophoresis

• involved serum free light chain (SFLC) concentration ≥ 10 mg/dL (100 mg/L) and an abnormal SFLC ratio

• Have adequate organ function including:

• Absolute neutrophil count (ANC) ≥ 1000/microliter

• Platelet (PLT) count ≥ 75,000/microliter

• Hemoglobin (Hgb) ≥ 8.0 g/dL

• Total bilirubin ≤ 1.5 x upper limit of normal (ULN) (if total is elevated check direct and, if normal, participant is eligible)

• Aspartate transaminase (AST) and alanine aminotransferase (ALT) are ≤ 3 x ULN

• Serum creatinine ≤ 3.0 mg/dL.

• Have an Eastern Cooperative Oncology Group performance status (ECOG PS) score of ≤ 2.

• Have discontinued all previous therapies for cancer, including chemotherapy, surgery, and radiotherapy for at least 2 weeks (6 weeks for mitomycin-C or nitrosoureas) before study enrollment and recovered from the acute effects of therapy.

• Males and females with reproductive potential: Must agree to use medically approved contraceptive precautions during the study and for 4 months following the last dose of study drug.

• Females with childbearing potential: Must have had a negative urine or serum pregnancy test <7 days before the first dose of study drug.

• Have an estimated life expectancy of ≥16 weeks, in the opinion of the investigator.

Exclusion Criteria:

• Have received treatment within 30 days of the initial dose of study drug with an experimental agent for non-cancer indications that has not received regulatory approval for any indication.

• Have one or more serious preexisting medical conditions that, in the opinion of the investigator, would preclude participation in this study.

• Have an uncontrolled infection.

• Females who are pregnant or breastfeeding.

• Have known positive test results for human immunodeficiency virus (HIV), hepatitis B*, or hepatitis C antibodies (HCAb).

• Have evidence of or test positive for hepatitis B. A positive test for hepatitis B is defined as:

1. positive for hepatitis B surface antigen (HBsAg+). OR

2. positive for anti-hepatitis B core antibody and positive for hepatitis B deoxyribonucleic acid (HBV DNA).

OR

3. positive for anti-hepatitis B surface antibody (HBsAb+) and positive for hepatitis B deoxyribonucleic acid (HBV DNA).

• Have ≥ Grade 2 peripheral neuropathy or any grade with pain as assessed using the Common Terminology Criteria for Adverse Events, version 4.03 (CTCAE v 4.03).

• Have previously received an allogenic hematopoietic stem cell transplant.

• Have previously received treatment with an experimental agent that targets B-cell activating factor (BAFF).

• Have a corrected QT (QTc) interval >470 msec on their baseline electrocardiogram (ECG).

• Have interstitial pneumonitis (interstitial pneumonia) or pulmonary fibrosis manifested as opacity on chest X-ray or computed tomography (CT) scan.

• Have had another active malignancy within the past 5 years.