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NCT07483268

A Prospective Study of Stapokibart Injection in Patients With CRSwNP

Active, enrolled Last updated 3 June 2026
What this trial tests

trial testing Stapokibart in CRSWNP in 600 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
29 May 2026
Primary endpoint
1 December 2027
1 February 2028

Quick facts

Lead sponsorChengdu Kangnuoxing Biopharma,Inc.
StatusActive, enrolled
Study typeOBSERVATIONAL
Enrollment600
Start date29 May 2026
Primary completion1 December 2027
Estimated completion1 February 2028
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Chengdu Kangnuoxing Biopharma,Inc. — full company profile →

Who can join

18 and older, any sex, with CRSWNP. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

This study is a open label, prospective study to evaluate the safety of Stapokibart Injection in subjects with CRSwNP.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Stapokibart

Trials testing the same drug.

Other recruiting trials for CRSWNP

Currently open trials in the same condition.

Other Chengdu Kangnuoxing Biopharma,Inc. 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/NCT07483268.

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