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Ascletis Pharma (China) Co clinical trials

Also registered as Ascletis Pharma (China)
Source: ClinicalTrials.gov, U.S. National Library of Medicine and the EU Clinical Trials Information System (CTIS) — current trials in our USA, UK and EU (CTIS) registers with Ascletis Pharma (China) Co as lead sponsor. Synced 26 Sep 2026
6Current trials
4Recruiting now
3Drugs in these trials
3Trial registers
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 — Top 14 finalist
Compiled from ClinicalTrials.gov and CTIS registry records · Last verified · Editorial standards
At a glance

Ascletis Pharma (China) Co is the lead sponsor of 6 current clinical trials in our USA, UK and EU (CTIS) registers. 4 are recruiting patients now. The most common phase is Phase 3. The drugs named most often in its trials are ASC30, ASC30 A1 and Tirzepatide. The most-studied condition is Chronic Weight Management.

ClinicalTrials.gov trials by status

  • Recruiting4100%

Trials by phase

  • Phase 3250%
  • Phase 1250%
01

Clinical trials sponsored by Ascletis Pharma (China) Co

4 on ClinicalTrials.gov
StudyPhaseStatusStartRegisters
A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Efficacy of ASC50 Tables in Healthy Participants and Participants With Plaque Psoriasis
NCT07024602 · Plaque Psoriasis
Phase 1 Recruiting 2025-06 USA
A Study of Once-daily Oral ASC30 to Evaluate the Efficacy and Safety in Adult Participants With Obesity or Overweight With Weight-Related Comorbidities
NCT07743463 · Obesity, Overweight, Chronic Weight Management
Drug: ASC30 A1
Phase 3 Recruiting 2026-08 UK, USA
A Study of Once-daily Oral ASC30 to Evaluate the Efficacy and Safety in Adult Participants With Obesity or Overweight With Type 2 Diabetes
NCT07743450 · ClinicalTrials.gov ↗ · Obesity, Overweight, Chronic Weight Management
Drug: ASC30 A1
Phase 3 Recruiting 2026-08 UK, USA
A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ASC35 Injection in Participants With Obesity or Overweight
NCT07842640 · ClinicalTrials.gov ↗ · Chronic Weight Management
Phase 1 Recruiting 2026-08 USA

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Titles and statuses are copied from the registry as published.

02

Ascletis Pharma (China) Co in the EU trials register (CTIS)

2 trials

Authorised or ongoing trials in the EU Clinical Trials Information System with Ascletis Pharma (China) Co as sponsor. Some are the same study as a ClinicalTrials.gov record above; the two registries share no common ID. Trials with a site in Ireland are listed first.

StudyPhaseStatusCountries
A Phase III, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Once-Daily oral ASC30 in Adult Participants with Obesity or Overweight with Weight-Related Comorbidities (AURORA-1)
2026-526172-23-00 · Nutritional and Metabolic Diseases
Drug: ASC30
Phase 3 Authorised Germany, Greece, Czechia
A Phase III, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Once-Daily Oral ASC30 in Adult Participants with Obesity or Overweight with Type 2 Diabetes Mellitus (AURORA-2)
2026-526336-39-00 · Nutritional and Metabolic Diseases
Drug: ASC30
Phase 3 Authorised Germany, Czechia, Greece + 1 more
03

Drugs in Ascletis Pharma (China) Co trials

3 compounds

Drugs and biologicals named as interventions in these trials, with the number of this sponsor's trials that name each one. Placebos and generic comparators are excluded.

04

Conditions in Ascletis Pharma (China) Co trials

5 conditions
05

By trial register

RegisterTrialsRecruiting
Clinical trials in USA44
Clinical trials in UK22
EU register (CTIS)2—

A trial with sites in more than one country appears in each of those registers.

06

Other sponsors in Chronic Weight Management

SponsorTrials
Gasherbrum Bio, Inc., a wholly owned subsidiary of Structure Therapeutics2

Sponsors with the most current trials registered for this condition.

07

Questions about Ascletis Pharma (China) Co trials

How many clinical trials does Ascletis Pharma (China) Co sponsor?

Ascletis Pharma (China) Co is the lead sponsor of 4 current trials on ClinicalTrials.gov in our USA and UK registers, and 2 authorised or ongoing trials in the EU register (CTIS), as of the registry sync on 26 September 2026. Completed and withdrawn studies are not counted.

Are Ascletis Pharma (China) Co trials recruiting?

Yes. 4 of its 4 ClinicalTrials.gov trials are recruiting. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Which drugs is Ascletis Pharma (China) Co testing?

Its current trials name 3 drugs and biologicals as interventions. The most frequent are ASC30 (2), ASC30 A1 (2) and Tirzepatide (1). The number in brackets is how many of its trials name each drug.

Where does this information come from?

Every trial, status, phase and condition on this page is copied from public ClinicalTrials.gov and EU CTIS records by a daily sync, grouped by the sponsor name each registry records. It says nothing about the organisation beyond its registered trials, and it is not medical advice.

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How this page is built

Everything on this page is copied from public registry records — it is not written from memory, and nothing here describes the organisation beyond its registered trials. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our trial registers and groups every current trial by its lead sponsor name, ignoring legal-form suffixes such as Inc. or Ltd. A small, hand-checked list joins the same organisation's different registry names (for example its EU legal entity). There is no AI drafting and no per-sponsor editorial pass. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The the registries data on this page was last retrieved on 26 Sep 2026.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.