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NCT07321678 · ClinicalTrials.gov registry record · Phase 2

A Study to Evaluate the Efficacy, Safety, and Tolerability of ASC30 Tablets in Participants With Type 2 Diabetes Mellitus

A Phase 2 study of T2DM (Type 2 Diabetes Mellitus), sponsored by Ascletis Pharma (China) Co., Limited.

Recruiting
Registry status
Phase 2
Development phase
100
Enrollment target
8
Study locations

NCT07321678: Recruiting Phase 2 study of T2DM (Type 2 Diabetes Mellitus), sponsored by Ascletis Pharma (China) Co., Limited.

NCT07321678 is a Phase 2 study of T2DM (Type 2 Diabetes Mellitus) that is actively recruiting participants, run by Ascletis Pharma (China) Co., Limited. The registered enrollment target is 100 participants, below the 210-participant average among 4 other T2DM (Type 2 Diabetes Mellitus) trials with a reported enrollment target (52% lower). The trial reports 8 study locations across 6 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07321678, a Phase 2 study of T2DM (Type 2 Diabetes Mellitus), is actively recruiting participants, sponsored by Ascletis Pharma (China) Co., Limited.

RECRUITING
Registry status
Phase 2
Development phase
100 participants
Enrollment target
8
Study locations

Study Summary

This randomized, double-blind, placebo-controlled Phase II study is designed to evaluate the efficacy, safety, and tolerability of ASC30 oral tablets formulation in participants with Type 2 Diabetes Mellitus

Interventions

  • DRUG Placebo
  • DRUG ASC30 tablets

Study Locations (8)

California

  • Ascletis Clinical Site - Riverside
  • Ascletis Clinical Site - San Jose

Florida

  • Ascletis Clinical Site - Miami
  • Ascletis Clinical Site - Miami

Colorado

  • Ascletis Clinical Site - Denver

Georgia

  • Ascletis Clinical Site - Decatur

Missouri

  • Ascletis Clinical Site - Springfield

Texas

  • Ascletis Clinical Site - San Antonio

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2026-01
Est. Completion 2026-08
Phase Phase 2

What NCT07321678 shows while recruiting

NCT07321678 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 210-participant average among 4 other T2DM (Type 2 Diabetes Mellitus) trials with a reported enrollment target (52% lower).

The record links to 1 condition, with T2DM (Type 2 Diabetes Mellitus) appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT07321678 lists 8 locations in 6 states (California, Florida, Colorado).

Frequently Asked Questions

What is clinical trial NCT07321678 about?

NCT07321678 is a clinical study titled "A Study to Evaluate the Efficacy, Safety, and Tolerability of ASC30 Tablets in Participants With Type 2 Diabetes Mellitus". This randomized, double-blind, placebo-controlled Phase II study is designed to evaluate the efficacy, safety, and tolerability of ASC30 oral tablets formulation in participants with Type 2 Diabetes Mellitus

What is the current status of trial NCT07321678?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 100 participants. The study started on 2026-01. Estimated completion is 2026-08.

What conditions does trial NCT07321678 study?

This clinical trial studies the following conditions: T2DM (Type 2 Diabetes Mellitus).

What interventions are being tested in trial NCT07321678?

The interventions under investigation include: Placebo (DRUG), ASC30 tablets (DRUG).

Who is sponsoring clinical trial NCT07321678?

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

Where is trial NCT07321678 being conducted?

This trial has 8 study locations across California, Colorado, Florida, Georgia, Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

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Source: ClinicalTrials.gov NCT07321678, the US trial registry maintained by the National Library of Medicine. NCT07321678 (mid enrollment · multi site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.