A Study Evaluating the Effects of Siltuximab on the Heart in Patients With Monoclonal Gammopathy of Undetermined Significance, Smoldering Multiple Myeloma, or Indolent Multiple Myeloma
Primary Purpose
Monoclonal Gammopathy of Undetermined Significance, Multiple Myeloma, Plasma Cell Neoplasm
Status
Completed
Phase
Phase 1
Locations
International
Study Type
Interventional
Intervention
Siltuximab
Sponsored by
About this trial
This is an interventional treatment trial for Monoclonal Gammopathy of Undetermined Significance focused on measuring Monoclonal Gammopathy of Undetermined Significance, Smoldering Multiple Myeloma, Indolent Multiple Myeloma, QT, Siltuximab, CNTO 328, IL-6, Monoclonal Antibody
Eligibility Criteria
Inclusion Criteria:
- Diagnosis of MGUS (measurable serum M-protein < 3 g/dL AND clonal bone marrow plasma cells < 10% without any end organ damage), SMM (measurable serum M-protein = 3 g/dL OR clonal bone marrow plasma cells = 10% without any end organ damage) or IMM (measurable serum M-protein = 3 g/dL OR clonal bone marrow plasma cells = 10% and = 3 lytic bone lesions but no other end organ damage)
- Qualifying ECG results that will be checked by a central laboratory
- Negative urine drug screen for substances of abuse
- Qualifying hematology and chemistry laboratory results.
Exclusion Criteria:
- Diagnosis of symptomatic multiple myeloma
- Prior exposure to approved or investigational myeloma treatments
- Prior exposure to agents targeting IL-6 or the IL-6 receptor
- Significant cardiac disease
- Skin condition likely to interfere with ECG electrode placement, breast implant, or thoracic surgery
- Received medications known to affect the QT interval
- Vaccination with live, attenuated vaccines within 4 weeks
- Major surgery or radiation within 4 weeks
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
001
Arm Description
Siltuximab 15mg/kg IV infusion every 3 weeks for 4 cycles. If applicable extended dosing of 15 mg/kg IV infusion every 4 weeks for up to 2 years.
Outcomes
Primary Outcome Measures
QTc interval
Secondary Outcome Measures
Additional safety evaluations
Efficacy evaluations
Pharmacokinetic and Pharmacodynamic evaluations
Full Information
NCT ID
NCT01219010
First Posted
September 23, 2010
Last Updated
January 16, 2015
Sponsor
Janssen Research & Development, LLC
1. Study Identification
Unique Protocol Identification Number
NCT01219010
Brief Title
A Study Evaluating the Effects of Siltuximab on the Heart in Patients With Monoclonal Gammopathy of Undetermined Significance, Smoldering Multiple Myeloma, or Indolent Multiple Myeloma
Official Title
A Study of Siltuximab (Anti-IL-6 Monoclonal Antibody) Effects on the QT Interval in Subjects With Monoclonal Gammopathy of Undetermined Significance, Smoldering Multiple Myeloma, or Indolent Multiple Myeloma
Study Type
Interventional
2. Study Status
Record Verification Date
January 2015
Overall Recruitment Status
Completed
Study Start Date
October 2010 (undefined)
Primary Completion Date
June 2012 (Actual)
Study Completion Date
March 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Janssen Research & Development, LLC
4. Oversight
5. Study Description
Brief Summary
The purpose of this study is to determine if siltuximab has an effect on the heart function measured by ECG recordings and more specifically to determine if siltuximab has an effect on the QT interval in patients with Monoclonal Gammopathy of Undetermined Significance (MGUS), Smoldering Multiple Myeloma (SMM) or Indolent Multiple Myeloma (IMM). The study will also look to see if siltuximab may be useful in treating patients with MGUS, SMM or IMM.
Detailed Description
This is a research study with an experimental drug called siltuximab (also known as CNTO 328). Currently there are studies with siltuximab, completed or ongoing, in patients with blood cancers such as multiple myeloma and Castleman's disease and with solid tumors such as kidney, ovarian and prostate cancer, to see if siltuximab is safe and to determine what effects it has on these types of cancer. This study is being done in patients with Monoclonal Gammopathy of Undetermined Significance (MGUS), Smoldering Multiple Myeloma (SMM) or Indolent Multiple Myeloma (IMM) to determine if siltuximab has an effect on heart function measured by ECG recordings, and more specifically to determine if siltuximab has any effect on the QT interval. MGUS, SMM and IMM patients usually go on to develop active multiple myeloma which is a type of cancer that affects the blood and bone marrow. The cancer cells in the bone marrow can cause the normal bone marrow cells to breakdown. This can result in low levels of red blood cells (which may make the patient feel tired or fatigued), low levels of white blood cells (which may increase the patient's chances of infections) or low levels of platelets (which may increase risk of bleeding). The cancer cells can cause damage to the normal bone. This can cause bone pain, bone fractures, and can increase the level of calcium in the blood. The cancer cells also make proteins (called M-proteins), which can result in damage to other organs, especially the kidneys. Siltuximab is a chimeric (part mouse and part human) antibody (immunoglobulin that is important for fighting infection). It does this by blocking another small protein called Interleukin 6 (IL-6). The body makes IL-6 naturally, and at normal levels it is important for the inflammatory response. But high levels of IL-6 can help cancer cells grow and interfere with chemotherapy drugs killing cancer cells. Cancer-related sicknesses such as weight loss, bone weakening, and depression have been linked to high levels of IL-6. This study will also look to see if siltuximab may be useful in treating patients with MGUS, SMM or IMM. All participating patients will be in the study for about 6 months and will receive siltuximab four (4) times every 3 weeks at a dose of 15mg per kg bodyweight. Siltuximab is given as a 1 hour intravenous infusion, through a small tube that goes directly into the vein. Following this treatment period, patients showing a response, defined as a 50% or higher reduction in M-protein in their blood/urine, may be allowed to continue treatment with siltuximab 15mg/kg every 4 weeks for up to 2 years.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Monoclonal Gammopathy of Undetermined Significance, Multiple Myeloma, Plasma Cell Neoplasm
Keywords
Monoclonal Gammopathy of Undetermined Significance, Smoldering Multiple Myeloma, Indolent Multiple Myeloma, QT, Siltuximab, CNTO 328, IL-6, Monoclonal Antibody
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Actual)
8. Arms, Groups, and Interventions
Arm Title
001
Arm Type
Experimental
Arm Description
Siltuximab 15mg/kg IV infusion every 3 weeks for 4 cycles. If applicable extended dosing of 15 mg/kg IV infusion every 4 weeks for up to 2 years.
Intervention Type
Biological
Intervention Name(s)
Siltuximab
Intervention Description
15mg/kg IV infusion every 3 weeks for 4 cycles. If applicable extended dosing of 15 mg/kg IV infusion every 4 weeks for up to 2 years.
Primary Outcome Measure Information:
Title
QTc interval
Time Frame
Screening through Week 10
Secondary Outcome Measure Information:
Title
Additional safety evaluations
Time Frame
6 months and, if eligible, up to 2 years of extended treatment
Title
Efficacy evaluations
Time Frame
6 months and, if eligible, up to 2 years of extended treatment
Title
Pharmacokinetic and Pharmacodynamic evaluations
Time Frame
6 months and, if eligible, up to 2 years of extended treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosis of MGUS (measurable serum M-protein < 3 g/dL AND clonal bone marrow plasma cells < 10% without any end organ damage), SMM (measurable serum M-protein = 3 g/dL OR clonal bone marrow plasma cells = 10% without any end organ damage) or IMM (measurable serum M-protein = 3 g/dL OR clonal bone marrow plasma cells = 10% and = 3 lytic bone lesions but no other end organ damage)
Qualifying ECG results that will be checked by a central laboratory
Negative urine drug screen for substances of abuse
Qualifying hematology and chemistry laboratory results.
Exclusion Criteria:
Diagnosis of symptomatic multiple myeloma
Prior exposure to approved or investigational myeloma treatments
Prior exposure to agents targeting IL-6 or the IL-6 receptor
Significant cardiac disease
Skin condition likely to interfere with ECG electrode placement, breast implant, or thoracic surgery
Received medications known to affect the QT interval
Vaccination with live, attenuated vaccines within 4 weeks
Major surgery or radiation within 4 weeks
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Janssen Research & Development, LLC Clinical Trial
Organizational Affiliation
Janssen Research & Development, LLC
Official's Role
Study Director
Facility Information:
City
Chicago
State/Province
Illinois
Country
United States
City
Dallas
State/Province
Texas
Country
United States
City
Houston
State/Province
Texas
Country
United States
City
Antwerpen
Country
Belgium
City
Gent
Country
Belgium
City
Izhevsk
Country
Russian Federation
City
Moscow N/A
Country
Russian Federation
City
Nizhni Novgorod
Country
Russian Federation
12. IPD Sharing Statement
Links:
URL
http://filehosting.pharmacm.com/DownloadService.ashx?client=CTR_JNJ_6051&studyid=213&filename=CR017452_CSR.pdf
Description
A Study of Siltuximab (Anti-IL-6 Monoclonal Antibody) Effects on the QT Interval in Subjects with Monoclonal Gammopathy of Undetermined Significance, Smoldering Multiple Myeloma, or Indolent Multiple Myeloma
Learn more about this trial
A Study Evaluating the Effects of Siltuximab on the Heart in Patients With Monoclonal Gammopathy of Undetermined Significance, Smoldering Multiple Myeloma, or Indolent Multiple Myeloma
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