ULM University Medical Centre
Ulm, 89075, Germany
Location status: Recruiting
NCT Number: NCT07220772
This study is researching an experimental drug called mibavademab. The study is focused on patients with a condition called monogenic obesity. Monogenic obesity is caused by a change in the leptin gene that keeps it from working properly. This causes the body to not be able to feel full or control feelings of hunger.
The aim of the study is to see how well mibavademab controls the body weight and how safe it is.
The study is looking at several other research questions, including:
* How much mibavademab is in the blood at different times * Whether the body makes proteins called antibodies against mibavademab (which could stop mibavademab from working as well or could lead to side effects) * What side effects may happen from taking mibavademab
Interested in participating?
Request Info2 year and older
All sexes
Interventional
Phase 3
Ulm, 89075, Germany
Location status: Recruiting
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Key Inclusion Criteria:
Key Exclusion Criteria:
NOTE: Other Protocol-defined Inclusion/Exclusion Criteria Apply
Administered as per the protocol
Other names: REGN4461
Time frame: Baseline to Week 24
Time frame: Baseline to Week 52
Time frame: Baseline, Through Week 52
Time frame: Baseline, Through Week 52
Time frame: Baseline, Through Week 52
Time frame: Baseline, Through Week 52
Participants aged ≥18 years
Time frame: Baseline, Through Week 52
Time frame: Baseline, Through Week 52
Time frame: Baseline, Through Week 52
Time frame: Baseline, Through Week 52
Time frame: Baseline, Through Week 52
Symptoms of Hyperphagia - Caregiver Version© is completed by a caregiver. Symptoms of Hyperphagia - Patient Version© is completed by the participants who are aged <12 years or for participants who are unable to self-complete. The questionnaires both assesses the frequency of hunger symptoms on a categorical scale (Never, 1 or 2 times, 3 or more times) over the past 24 hours and are scored combining the total scores across the items. Higher scores indicate greater severity.
Time frame: Baseline, Through Week 52
For participants who are aged <12 years or for participants who are unable to self-complete, the Impacts of Hyperphagia - Caregiver Version© is completed by a caregiver. For participants aged ≥12 years who are able to self-report, the Impacts of Hyperphagia - Patient Version© is completed by the participant. Both questionnaires assess the impact of hyperphagia on a categorical scale (range: not at all, a little, moderately, a great deal). The participant version is scored using a total score across the 5 items. The caregiver version is scored separately for each section. Higher scores indicate a greater impact of hyperphagia.
Time frame: Baseline, Through Week 52
The Daily Hunger Assessment is a daily, single item measuring hunger for participants aged ≥12 years who are able to self-complete, participants are asked to rate their highest level of hunger over for the day, where "0" is "not hungry at all" to "10" the hungriest possible."
Time frame: Through Week 65
Time frame: Through Week 65
Time frame: Through Week 65
Time frame: Through Week 65
Time frame: Through Week 65
Contact information is provided by the study sponsor or research team.
Regeneron Pharmaceuticals
Industry
An Open-Label Study of Mibavademab (REGN4461), a Leptin Receptor Agonist, for the Treatment of Monogenic Obesity Due to Biallelic Loss of Function Variants of the LEP Gene
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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