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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 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.
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
Conditions Studied
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
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2026-01 |
| Est. Completion | 2026-08 |
| Phase | Phase 2 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07321678
The ClinicalTrials.gov registry entry for NCT07321678 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 210-participant average among 4 other T2DM (Type 2 Diabetes Mellitus) trials with a reported enrollment target (52% lower). The listed sponsor is Ascletis Pharma (China) Co., Limited, which has 6 total studies on file at ClinicalTrials.gov.
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 reports 8 study locations spanning 6 distinct geographic areas - top geographies include 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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Related
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