A Phase 2 Study to Assess Efficacy and Safety of LB54640 in Patients With Genetic Obesity

NCT06041841 · Status: NOT_YET_RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 4

Last updated 2023-11-02

No results posted yet for this study

Summary

The purpose of the study was to assess the efficacy of LB54640 in participants with rare genetic disorders of obesity

Conditions

  • POMC Deficiency Obesity
  • PCSK1 Deficiency Obesity
  • LEPR Deficiency Obesity

Interventions

DRUG

LB54640

LB54640 QD Oral

Sponsors & Collaborators

  • LG Chem

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
12 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-12-31
Primary Completion
2024-12-31
Completion
2025-12-31
FDA Drug
Yes

Countries

  • France
  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06041841 on ClinicalTrials.gov