A Study of LY3502970 in Participants With Obesity or Overweight With Weight-related Comorbidities

Part of paid clinical trials in Anaheim, California.

Sponsor
Eli Lilly and Company
Study ID
NCT05051579
Phase
PHASE2
Status
Completed

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - 75 Years
Healthy Volunteers
Not accepted

Interventions

  • LY3502970 — DRUG
    Administered orally
  • Placebo — DRUG
    Administered orally

Study Details

The main purpose of the study was to assess the effect of LY3502970 in participants who have obesity or are overweight.

Key Dates

Start date
Sep 29, 2021
Status verified
Aug 2023
Primary completion
Aug 25, 2022
Completion
Nov 22, 2022

Study Design

Enrollment
272 participants (actual)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: 12 milligram (mg) LY3502970
    Participants received maintenance dose 12 mg with dose escalation starting from 3 mg,6 mg and then 12 mg LY3502970 administered orally once daily until 36 weeks.
  • Experimental: 24 mg LY3502970
    Participants received maintenance dose 24 mg with dose escalation starting from 3 mg, 6 mg, 8 mg,12 mg and then 24 mg LY3502970 administered orally once daily until 36 weeks.
  • Experimental: 36 mg-1 LY3502970
    Participants received maintenance dose 36 mg with dose escalation starting from 2 mg, 3 mg, 6 mg, 8 mg, 12 mg, 24 mg and then 36 mg LY3502970 administered orally once daily until 36 weeks.
  • Experimental: 36 mg-2 LY3502970
    Participants received maintenance dose 36 mg with dose escalation starting from 3 mg, 6 mg,12 mg, 24 mg and then 36 mg LY3502970 administered orally once daily until 36 weeks.
  • Experimental: 45 mg-1 LY3502970
    Participants received maintenance dose 45 mg with dose escalation starting from 3 mg, 6 mg, 8 mg, 12 mg, 24 mg, 36 mg and then 45 mg LY3502970 administered orally once daily until 36 weeks.
  • Experimental: 45 mg-2 LY3502970
    Participants received maintenance dose 45 mg with dose escalation starting from 2 mg, 3 mg, 6 mg, 12 mg, 24 mg, 36 mg and then 45 mg LY3502970 administered orally once daily until 36 weeks.
  • Placebo Comparator: Placebo
    Participants received placebo administered orally once daily until 36 weeks.

Primary Outcome Measure

Percent Change From Baseline in Body Weight in LY3502970 and Placebo [ Time Frame: Baseline, Week 26 ]

Locations (18)

FacilityCityStateZIPSite coordinators
Anaheim Clinical Trials, LLCAnaheimCalifornia92801-
John Muir Physician Network Research CenterConcordCalifornia94520-
NorCal Medical Research, IncGreenbraeCalifornia94904-
Valley Clinical Trials, Inc.NorthridgeCalifornia91325-
Norcal Endocrinology & Internal MedicineSan RamonCalifornia94583-
Elite Clinical TrialsBlackfootIdaho83221-
Rocky Mountain Clinical ResearchIdaho FallsIdaho83404-
StudyMetrix ResearchCity of Saint PetersMissouri63303-
Premier ResearchTrentonNew Jersey08611-
Lillestol ResearchFargoNorth Dakota58104-
Intend Research, LLCNormanOklahoma73069-
Capital Area Research, LLCCamp HillPennsylvania17011-
Preferred Primary Care Physicians, Preferred Clinical Research-St. ClairPittsburghPennsylvania15243-
Dallas Diabetes Research CenterDallasTexas75230-
Diabetes and Thyroid Center of Fort WorthFort WorthTexas76132-
Texas Diabetes & Endocrinology, P.A.Round RockTexas78681-
National Clinical Research, IncRichmondVirginia23294-
St. Vincent Hospital d/b/a Prevea HealthGreen BayWisconsin54303-

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