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NCT06835296

A Study of Oral YUQ-A1007 in Healthy Volunteers

Completed Phase 1 Last updated 26 December 2025
What this trial tests

Phase 1 trial testing YUQ-A1007 is a novel gut-enriched AhR agonist. This compound is undergoing preclinical development, and comprehensive nonclinical studies. in Healthy in 47 participants. Completed in 30 September 2025.

Timeline
20 March 2025
Primary endpoint
30 September 2025
30 September 2025

Quick facts

Lead sponsorAllianthera (Suzhou) Biopharmaceuticals Co., Ltd.
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designsequential
Maskingnone
Primary purposetreatment
Enrollment47
Start date20 March 2025
Primary completion30 September 2025
Estimated completion30 September 2025
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Allianthera (Suzhou) Biopharmaceuticals Co., Ltd.

Who can join

Adults 18 to 65, any sex, with Healthy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

YUQ-A1007 is a novel gut-enriched AhR agonist. The nonclinical pharmacology study indicated that YUQ-A1007 has the potential to treat IBD. YUQ-A1007 has not been evaluated in human clinical studies. This study is first-in-human (FIH) study of YUQ-A1007. The goal of this trial is to evaluate the safety, tolerability, and pharmacokinetics of oral YUQ-A1007.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06835296.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing