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

NCT ID: NCT01556438

Last Updated: 2019-03-20

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 16 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-07-31
• Study Completion Date: 2015-08-31

Brief 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).

Detailed Description

The study has 3 cohorts. Cohort 2 and cohort 2-SC will be conducted in parallel with some data presented combined.

Cohort 1 - Participants will receive 100 mg Tabalumab (LY2127399) intravenously (IV), 1.3 milligram per square meter (mg/m^2) bortezomib IV, and 20 mg dexamethasone orally.

Cohort 2 - Participants will receive 300 mg Tabalumab (LY2127399) IV, 1.3 mg/m^2 bortezomib IV, and 20 mg dexamethasone orally.

Cohort 2-SC - Participants will receive 300 mg Tabalumab (LY2127399) IV, 1.3 mg/m^2 bortezomib subcutaneously (SC), and 20 mg dexamethasone orally.

Cohort 2-SC was added per protocol amendment in February 2013.

Conditions

Multiple Myeloma

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

100 mg Tabalumab+Bortezomib (BTZ)IV+Dexamethasone (Dex)

Cohort 1. 100 mg tabalumab (LY2127399) intravenously (IV) on day 1 of each cycle, each cyle is 21 days. Bortezomib (BTZ), 1.3 milligram per square meter (mg/m\^2), IV on days 1, 4, 8, 11 of Cycle 1-8, then on days 1, 8, 15, 22 from Cycle 9 onward. Oral dexamethasone (Dex), 20 mg/day, on day of and day after BTZ.

Group Type: EXPERIMENTAL

Tabalumab

Intervention Type: BIOLOGICAL

Administered IV

Bortezomib IV

Intervention Type: DRUG

Administered IV

Dexamethasone

Intervention Type: DRUG

Administered orally

300 mg Tabalumab+BTZ IV+Dex

Cohort 2. 300 mg tabalumab (LY2127399) IV on day 1 of each cycle, each cycle is 21 days. BTZ, 1.3 mg/m\^2, IV on days 1, 4, 8, 11 of Cycle 1-8, then on days 1, 8, 15, 22 from Cycle 9 onward. Oral dex, 20 mg/day, on day of and day after BTZ.

Group Type: EXPERIMENTAL

Tabalumab

Intervention Type: BIOLOGICAL

Administered IV

Bortezomib IV

Intervention Type: DRUG

Administered IV

Dexamethasone

Intervention Type: DRUG

Administered orally

300 mg Tabalumab+BTZ SC+Dex

Cohort 2-SC. 300 mg tabalumab (LY2127399)IV on day 1 of each cycle, each cycle is 21 days. BTZ, 1.3 mg/m\^2, subcutaneously (SC) on days 1, 4, 8, 11 of Cycle 1-8, then on days 1, 8, 15, 22 from Cycle 9 onward. Oral dex, 20 mg/day, on day of and day after BTZ. Cohort 2-SC was added per protocol amendment in February 2013.

Group Type: EXPERIMENTAL

Tabalumab

Intervention Type: BIOLOGICAL

Administered IV

Bortezomib SC

Intervention Type: DRUG

Administered SC

Dexamethasone

Intervention Type: DRUG

Administered orally

Interventions

Tabalumab

Administered IV

Intervention Type: BIOLOGICAL

Bortezomib IV

Administered IV

Intervention Type: DRUG

Bortezomib SC

Administered SC

Intervention Type: DRUG

Dexamethasone

Administered orally

Intervention Type: DRUG

Other Intervention Names

LY2127399

Eligibility 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.

• Minimum Eligible Age: 20 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Eli Lilly and Company

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST)

Role: STUDY_DIRECTOR

Eli Lilly and Company

Locations

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.

Aichi, , Japan

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.

Fukuoka, , Japan

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.

Kanagawa, , Japan

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.

Kyoto, , Japan

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.

Tokyo, , Japan

Countries

Japan

References

Iida S, Ogiya D, Abe Y, Taniwaki M, Asou H, Maeda K, Uenaka K, Nagaoka S, Ishiki T, Conti I, Tobinai K. Dose-escalation study of tabalumab with bortezomib and dexamethasone in Japanese patients with multiple myeloma. Cancer Sci. 2016 Sep;107(9):1281-9. doi: 10.1111/cas.13000. Epub 2016 Sep 1.

Reference Type: DERIVED

PMID: 27350068 (View on PubMed)

Other Identifiers

H9S-JE-JDCI

Identifier Type: OTHER

Identifier Source: secondary_id

14459

Identifier Type: -

Identifier Source: org_study_id