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UBT251 Injection Phase II Study (Overweight or Obesity)

NCT07177469 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 205

Last updated 2026-05-07

No results posted yet for this study

Summary

This randomized, double-blind, parallel, placebo-controlled phase II study to evaluate the efficacy and safety of UBT251 Injection in overweight/obese patients

Conditions

  • Obesity &Amp; Overweight

Interventions

DRUG

UBT251 Injection 2.0 mg and UBT251 Injection Placebo

UBT251 Injection and UBT251 Injection Placebo subcutaneously once weekly

DRUG

UBT251 Injection 4.0 mg (ID 0.5 mg) and UBT251 Injection Placebo

UBT251 Injection and UBT251 Injection Placebo subcutaneously once weekly

DRUG

UBT251 Injection 4.0 mg (ID 1.0 mg) and UBT251 Injection Placebo

UBT251 Injection and UBT251 Injection Placebo subcutaneously once weekly

DRUG

UBT251 Injection 6.0 mg and UBT251 Injection Placebo

UBT251 Injection and UBT251 Injection Placebo subcutaneously once weekly

Sponsors & Collaborators

  • The United Bio-Technology (Hengqin) Co., Ltd.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-03-14
Primary Completion
2025-10-22
Completion
2025-11-19

Countries

  • China

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 NCT07177469 on ClinicalTrials.gov