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NCT07002905 · ClinicalTrials.gov registry record · Phase 2

A Study to Evaluate the Efficacy, Safety, and Tolerability in Participants With Obesity or Overweight With Weight-Related Comorbidities

A Phase 2 study, sponsored by Ascletis Pharma (China) Co., Limited.

Completed
Registry status
Phase 2
Development phase
125
Enrollment target

NCT07002905: Completed Phase 2 study, sponsored by Ascletis Pharma (China) Co., Limited.

NCT07002905 is a Phase 2 study that has completed, run by Ascletis Pharma (China) Co., Limited. The registered enrollment target is 125 participants, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07002905, a Phase 2 study, has completed, sponsored by Ascletis Pharma (China) Co., Limited.

COMPLETED
Registry status
Phase 2
Development phase
125 participants
Enrollment target

Study Summary

This randomized, double-blind, placebo-controlled phase IIa study is designed to evaluate the efficacy, safety, and tolerability of ASC30 Tablets and ASC30 Tablets A1.

Interventions

  • DRUG ASC30 tablets or ASC30 tablets A1 or placebo

Trial Details

FieldValue
Enrollment Target 125 participants
Start Date 2025-07-03
Est. Completion 2025-12-08
Phase Phase 2

What the finished NCT07002905 record still lists

NCT07002905 is an interventional study that assigns participants to a tested intervention. The registered 125 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target.

The record links to 0 conditions, and to 1 intervention - of which ASC30 tablets or ASC30 tablets A1 or placebo is the first listed.

NCT07002905 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07002905 about?

NCT07002905 is a clinical study titled "A Study to Evaluate the Efficacy, Safety, and Tolerability in Participants With Obesity or Overweight With Weight-Related Comorbidities". This randomized, double-blind, placebo-controlled phase IIa study is designed to evaluate the efficacy, safety, and tolerability of ASC30 Tablets and ASC30 Tablets A1.

What is the current status of trial NCT07002905?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 125 participants. The study started on 2025-07-03. Estimated completion is 2025-12-08.

What interventions are being tested in trial NCT07002905?

The interventions under investigation include: ASC30 tablets or ASC30 tablets A1 or placebo (DRUG).

Who is sponsoring clinical trial NCT07002905?

This trial is sponsored by Ascletis Pharma (China) Co., Limited, which has 6 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07002905's enrollment target sits among peer trials

125 558th of 2000 higher than 1,437 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT07002905, the US trial registry maintained by the National Library of Medicine. NCT07002905 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.