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NCT05522439

A Study to Evaluate the Pharmacodynamic, Efficacy and Safety of SHR-1703 in Asthma Patients With Eosinophil Phenotype

Completed Phase 2 Last updated 28 May 2025
What this trial tests

Phase 2 trial testing SHR-1703 in Asthma With Eosinophilic Phenotype in 85 participants. Completed in 12 September 2024.

Timeline
22 December 2022
Primary endpoint
12 September 2024
12 September 2024

Quick facts

Lead sponsorJiangsu HengRui Medicine Co., Ltd.
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment85
Start date22 December 2022
Primary completion12 September 2024
Estimated completion12 September 2024
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Jiangsu HengRui Medicine Co., Ltd. — full company profile →

Who can join

Adults 18 to 75, any sex, with Asthma With Eosinophilic Phenotype. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to evaluate the Pharmacodynamic, Efficacy and Safety of SHR-1703 in Asthma Patients with Eosinophil Phenotype.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Therapeutic monoclonal antibodies in allergy: Targeting IgE, cytokine, and alarmin pathways.
    Eggel A, Pennington LF, Jardetzky TS. · · 2024 · cited 45× · PMID 39158477 · DOI 10.1111/imr.13380

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Other trials of SHR-1703

Trials testing the same drug.

Other Jiangsu HengRui Medicine Co., Ltd. trials

Trials by the same sponsor.

Verify against primary sources

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/NCT05522439.

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