Summary

Eligibility
for people ages 6-11 (full criteria)
Location
at UCLA
Dates
study started
study ends around
Principal Investigator
by Vibha Singhal (ucla)

Description

Summary

The main purpose of this study, performed under Master Protocol J4M-MC-PWMP (NCT06672549), is to evaluate the efficacy, safety, and pharmacokinetics of tirzepatide as an addition to healthy lifestyle in participants 6 to less than 12 years of age, with obesity. Participation in the study will last about 104 weeks.

Participants who have completed the primary 104-week PW02 study (including the 4-week safety follow-up period), will have the opportunity to receive an additional 156 weeks of treatment with tirzepatide as well as continuing the lifestyle intervention.

Official Title

Efficacy, Safety, and Pharmacokinetics of Tirzepatide Once Weekly Versus Placebo in Pediatric Participants 6 to Less Than 12 Years of Age Who Have Obesity: A Phase 3, Randomized, Double-Blind, Placebo-Controlled Trial

Keywords

Obesity, Pediatric, Children, Tirzepatide

Eligibility

You can join if…

Open to people ages 6-11

J4M-MC-PW02

  • Are 6 to less than 12 years of age (Tanner stage 1 to 5 inclusive)
  • Have:
    • a body weight of ≥ 40 kilograms (kg) (88 pounds), and
    • been diagnosed with obesity, as defined by BMI equal to or above the 95th percentile for age and sex, on age- and sex-specific growth chart

J4M-MC-PWMP

  • Have a history of at least 1 unsuccessful effort to lose sufficient body weight after participation in a structured lifestyle modification program (diet and exercise counseling for at least 3 months) prior to screening.
  • Obesity as defined by BMI equal to or above the 95th percentile for age and sex (on age- and gender-specific growth chart [CDC-NCHS, 2022])

You CAN'T join if...

J4M-MC-PW02

J4M-MC-PWMP

  • Have undergone or plan to undergo weight reduction procedure during the study, such as, but not limited to:
    • gastric bypass
    • sleeve gastrectomy
    • restrictive bariatric surgery, such as Lap-Band® gastric banding, or
    • any other procedure intended to result in weight reduction.
  • Have a diagnosis that is a secondary cause of obesity or have a history of abrupt onset of obesity suggesting a secondary cause, such as hypothalamic, monogenetic, syndromic, or endocrine causes.
  • Have type 1 diabetes or history of ketoacidosis, or hyperosmolar state.
  • Have HbA1c >9.0% (75 mmol/mol) as measured by central laboratory at screening.
  • Have a family or personal history of medullary thyroid carcinoma or Multiple Endocrine Neoplasia Syndrome Type 2.

Locations

  • UCLA Mattel Children's Hospital
    Los Angeles California 90095 United States
  • Childrens Hospital of Los Angeles
    Los Angeles California 90027 United States
  • Children's Hospital of Orange County
    Orange California 92868 United States

Lead Scientist at University of California Health

  • Vibha Singhal (ucla)
    HS Associate Clinical Professor, Pediatrics, Medicine. Authored (or co-authored) 15 research publications

Details

Status
not yet accepting patients
Start Date
Completion Date
(estimated)
Sponsor
Eli Lilly and Company
ID
NCT07817875
Phase
Phase 3 Obesity Research Study
Study Type
Interventional
Participants
Expecting 150 study participants
Last Updated