Evaluate the Effect of Obicetrapib in Patients With HeFH on Top of Maximum Tolerated Lipid-Modifying Therapies.

Part of paid clinical trials in Jonesboro, Arkansas.

Sponsor
NewAmsterdam Pharma
Study ID
NCT05425745
Phase
PHASE3
Status
Completed

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Obicetrapib — DRUG
    10 mg Obicetrapib tablet
  • Placebo — DRUG
    placebo tablet made to resemble active

Study Details

This study will be a placebo-controlled, double-blind, randomized, phase 3 study to Evaluate the Efficacy, Safety, and Tolerability of Obicetrapib in Participants with a History of Heterozygous Familial Hypercholesterolemia (HeFH).

Key Dates

Start date
Jul 25, 2022
Status verified
Jun 2025
Primary completion
May 28, 2024
Completion
May 28, 2024

Study Design

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

Arms

  • Placebo Comparator: Placebo
    one placebo tablet once daily
  • Experimental: Obicetrapib 10 mg
    one 10 mg Obicetrapib tablet once daily

Primary Outcome Measure

Percent Change in Low-Density Lipoprotein Cholesterol (LDL-C) From Baseline to Day 84 [PUC] [ Time Frame: 84 Days ]

Locations (20)

FacilityCityStateZIP
Site 01022JonesboroArkansas72401
Site 01015Toluca LakeCalifornia91602
Site 01009SarasotaFlorida34230
Site 01023BoiseIdaho83702
Site 01018ChicagoIllinois60602
Site 01012Iowa CityIowa52240
Site 01007Baton RougeLouisiana70809
Site 01005Port GibsonMississippi39105
Site 01006St LouisMissouri63130
Site 01011LincolnNebraska68510
Site 01004NorfolkNebraska68701
Site 01002MorristownNew Jersey07960
Site 01010New ProvidenceNew Jersey07901
Site 01001North MassapequaNew York11758
Site 01020MorgantonNorth Carolina28655
Site 01019Winston-SalemNorth Carolina27157
Site 01008ChattanoogaTennessee37405
Site 01016El PasoTexas79905
Site 01013HoustonTexas76706
Site 01014SuffolkVirginia23434

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