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H24LEAP2
Sponsor study identifier
interventional
18
0 countries
N/A
Study Start
November 30, 2026
EstimatedPlanned date reported by the registry; this milestone is not confirmed as achieved.
Primary Completion
August 1, 2027
EstimatedPlanned date reported by the registry; this milestone is not confirmed as achieved.
Study Completion
August 1, 2027
EstimatedPlanned date reported by the registry; this milestone is not confirmed as achieved.
This study investigates whether temporarily blocking the ghrelin receptor affects appetite and food intake in people with overweight or obesity. Ghrelin is a hormone that stimulates hunger; the researchers are using LEAP2, a naturally occurring hormone that blocks ghrelin's receptor, as a research tool to study what happens when ghrelin signaling is turned off for 24 hours. The study is a randomized, double-blind, placebo-controlled crossover trial. Eighteen adults with overweight or obesity (BMI ≥25 kg/m², elevated body fat percentage) will each complete two 24-hour study visits, at least 7 days apart: one with a continuous LEAP2 infusion and one with a saline placebo infusion, in random order. Neither participants nor most study staff will know which treatment is given on which visit. During each 24-hour visit, participants will receive a standardized liquid test meal followed by ad libitum (eat-until-comfortably-full) lunch, dinner, and breakfast meals, plus access to snacks. The main question the study aims to answer is whether LEAP2 reduces the total amount of food eaten over 24 hours compared to placebo. Additional measurements include blood glucose levels, subjective feelings of hunger and fullness (via questionnaires), stomach emptying rate, blood pressure and heart rate, and hormone levels (including growth hormone, FSH, and LH). Some participants will also undergo a small fat tissue biopsy to study how genes and proteins related to metabolism respond. The results are expected to improve understanding of how ghrelin and LEAP2 regulate appetite and metabolism in people with obesity, which may inform future approaches to treating obesity and related metabolic conditions.
Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.
August 1, 2027
EstimatedPlanned date reported by the registry; this milestone is not confirmed as achieved.
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Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.
September 28, 2026
Actual (reported)October 27, 2026
Actual (reported)November 30, 2026
EstimatedPlanned date reported by the registry; this milestone is not confirmed as achieved.
August 1, 2027
EstimatedPlanned date reported by the registry; this milestone is not confirmed as achieved.
August 1, 2027
EstimatedPlanned date reported by the registry; this milestone is not confirmed as achieved.
Food intake
Difference in total energy intake during the standardized ad libitum meals. Energy intake will be quantified as kilojoules (kJ) during the 24 hours
24 hours
Total food intake/24 hours
24 hours
Total food intake/24 hours
24 hours
Food intake lunch
5 hours after infusion start
Food intake dinner
11 hours after infusion start
Food intake breakfast
23 hours after infusion start
Growth hormone
24 hours
LH (luteinizing hormone)
24 hours
Acyl-ghrelin
24 hours
An intravenous infusion of LEAP2, an endogenous inverse agonist and competitive antagonist of the ghrelin receptor (GHSR), will be administered at 40 pmol/kg/min for 24 hours.
An intravenous infusion of isotonic saline (placebo) will be administered for 24 hours.
Continuous intravenous infusion of LEAP2 (Liver-Expressed Antimicrobial Peptide 2), an endogenous inverse agonist and competitive antagonist of the ghrelin receptor (GHSR), administered at 40 pmol/kg/min for 24 hours. LEAP2 inhibits ghrelin-mediated signaling involved in hunger regulation, gastric motility, and growth hormone secretion. This intervention enables investigation of the physiological relevance of ghrelin receptor activity during 24 hours in individuals with overweight or obesity.
First Submitted
September 28, 2026
First Posted
October 27, 2026
Study Start
November 30, 2026
EstimatedPlanned date reported by the registry; this milestone is not confirmed as achieved.
Primary Completion
Continuous intravenous infusion of isotonic saline (0.9% sodium chloride) for 24 hours. This placebo comparator is used to match the volume, rate, and duration of the active intervention (LEAP2) in a randomized, double-blind, crossover design. The placebo enables assessment of the physiological effects of ghrelin receptor blockade by LEAP2 in individuals with overweight or obesity.
Contact the study team to confirm eligibility.
August 1, 2027
Planned date reported by the registry; this milestone is not confirmed as achieved.
Study Completion
August 1, 2027
EstimatedPlanned date reported by the registry; this milestone is not confirmed as achieved.
Last Updated
October 27, 2026
Record last verified: 2026-10
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Source: ClinicalTrials.gov.
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