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Tirzepatide

Mounjaro, Zepbound, LY3298176

Quick Stats
Studies 183
Trials 100
Recruiting PHASE4 INTERVENTIONAL NCT06901245

Tirzepatide in PWS, HO and GNSO

View on ClinicalTrials.gov Updated Dec 15, 2025

Brief Summary

This research study is comparing the effectiveness of a weight loss medication called Tirzepatide in young adults with Prader-Willi Syndrome and/or hypothalamic obesity, as compared to young adults with obesity that is unrelated to a genetic syndrome or underlying medical cause. These groups will be given medication for 1 year to see how weight and other health factors are effected by the medication.

Detailed Description

This study is for the following individuals: * Age 18-26. * Have Prader-Willi Syndrome, Hypothalamic Obesity, or Obesity unrelated to a genetic syndrome or medical condition. * Have a BMI in the obesity range If you/your child decide to take part in the research study, you/your child would participate in the study for approximately 56-60 weeks. During this time the following can be expected: * Receive tirzepatide for once-weekly dosing. * Complete 6 in-person SCH study visits * Complete 4 telehealth visits. * Complete the following research procedures: * Medical Record Review * Vital Signs * Anthropometry (e.g., height, weight, waist measurements) * Physical Exams * Laboratory Tests (e.g., fasting blood draws, urine test) * Dual-Energy Absorptiometry (DXA) scans * Questionnaires

Interventions

Name: Tirzepatide
Type: DRUG
Description: Subjects will take Tirzepatide for 48 weeks

Primary Outcomes

Measure: Change in weight
TimeFrame: 48 weeks
Description: Weight will be measured in kilograms through anthropometric measurements. Change in percent weight from baseline to week 48 of treatment with tirzepatide in young adults with PWS, HO, GNSO and obesity will then be assessed.

Trial Information

NCT ID

NCT06901245

Status

Recruiting

Study Type

INTERVENTIONAL

Phases

PHASE4

Sponsor

Grace Kim

Last Updated

December 15, 2025