A Study of the Safety of Mibavademab in Pediatric and Adult Participants Switching From Metreleptin to Mibavademab for the Treatment of Generalized Lipodystrophy (GLD)
- Registration Number
- NCT06548100
- Lead Sponsor
- Regeneron Pharmaceuticals
- Brief Summary
This study is researching an experimental drug called mibavademab. The study is focused on participants with GLD who have been on metreleptin treatment for at least 6 months with no change in dose for the last 3 months.
The aim of the study is to see how safe and tolerable mibavademab is when switching from treatment with metreleptin.
The study is looking at several other research questions, including:
* What side effects may happen from taking mibavademab
* How much mibavademab is in the blood at different times
* Whether the body makes antibodies against mibavademab (which could make mibavademab less effective or could lead to side effects)
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 8
Inclusion Criteria
- Diagnosis of congenital or acquired GLD as defined by Multi-Society Practice Guidelines
- Treatment with metreleptin for ≥6 months at time of screening at a stable dose, defined as no change in dose within the last 3 months prior to screening
- Generally stable diet (based on participant's recall) and stable medication regimen for diabetes and/or dyslipidemia (in addition to metreleptin), for the last 3 months prior to screening
- Willing and able to comply with clinic visits and study-related procedures. Participants who are unable/unwilling to self-inject, but are willing to have a capable caregiver inject, are considered eligible
- Willing and able to provide, or have the treating physician provide, values of HbA1c and fasting triglycerides from at least 6 months prior to screening, as defined in the protocol
Key
Exclusion Criteria
- Treatment with over-the-counter or prescription medications for weight loss within 3 months prior to the screening visit
- Current chronic treatment with high-dose corticosteroids, as defined in the protocol
- Any malignancy, eg, lymphoma, within the past 1 year, prior to screening visit except for fully treated basal cell or squamous epithelial cell carcinomas of the skin or carcinoma in situ of the cervix or anus
- Estimated glomerular filtration rate (GFR) of <30 mL/min/1.73 m^2 based on chronic kidney disease epidemiology collaboration (CKD-EPI)/Schwartz equation at screening. Assessment can be repeated once
- History of heart failure hospitalization, diagnosis of a myocardial infarction, stroke, clinically significant arrhythmia, transient ischemic attack, unstable angina, percutaneous or surgical revascularization procedure, or intracardiac device placement within 3 months before the screening visit, as defined in the protocol
- Any physical examination findings and/or history of any illness that, in the opinion of the study investigator, might confound the results of the study or pose an additional risk to the participant by their participation in the study, as defined in the protocol
NOTE: Other protocol-defined inclusion / exclusion criteria apply
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description mibavademab mibavademab Patients switching from at least 6 months of therapy with metreleptin to mibavademab.
- Primary Outcome Measures
Name Time Method Severity of TEAEs Up to week 68 Incidence of treatment-emergent adverse events (TEAEs) Up to week 68
- Secondary Outcome Measures
Name Time Method Change in fasting plasma glucose Baseline, week 20 and week 52 Occurrence of HbA1c <7% Week 20 and week 52 Concentrations of total mibavademab in serum Up to week 68 Incidence of neutralizing antibodies (Nabs) to mibavademab Up to week 68 Percent change in fasting triglycerides Baseline, week 20 and week 52 Change in Hemoglobin A1c (HbA1c) Baseline, week 20 and week 52 Occurrence of HbA1c <6.5% Week 20 and week 52 Change in total insulin dose Baseline, week 20 and week 52 Occurrence of fasting triglycerides <200 mg/dL in participants treated with mibavademab Baseline, week 20 and week 52 Incidence of anti-drug antibodies (ADAs) to mibavademab Up to week 68 Occurrence of requiring therapy with insulin in participants treated with mibavademab Week 20 and week 52 Occurrence of fasting triglycerides <500 mg/dL in participants treated with mibavademab Baseline, week 20 and week 52 Titer of ADAs to mibavademab Up to week 68 Occurrence of fasting triglycerides <150 mg/dL in participants treated with mibavademab Baseline, week 20 and week 52
Trial Locations
- Locations (2)
National Institutes of Health
🇺🇸Bethesda, Maryland, United States
University of Michigan
🇺🇸Ann Arbor, Michigan, United States