Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT07459556

A Prospective Study of Stapokibart Injection in Patients With Seasonal Allergic Rhinitis (SAR)

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

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Conditions

SAR

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participants aged 18 years or older at the time of informed consent and provide voluntary informed consent to participate in the study before inclusion in the study.
  • Physician decision to treat the participant with Stapokibart Injection for SAR (according to the China-specific prescribing information) made prior to and independently of the participant's participation in the study.

Exclusion criteria

  • Known history of allergic reaction to Stapokibart Injection.
  • Participants currently or plan participating in any interventional clinical trial.
  • Participants with hematologic malignancies.
  • Women with pregnant.
  • Any condition that, in the opinion of the Investigator, may interfere with the participant's ability to participate in the study.

Treatment and study plan

Stapokibart

Biological

subcutaneous injection

Primary outcomes

  1. The incidence rate of adverse reactions (ADR).

    Time frame: From enrollment to the end of treatment at 10 weeks

    Number of of Adverse Reactions （ADRs） is calculated based on Adverse Events （AEs） and Serious Adverse Events （SAEs） that were assessed by the investigator as related to the study drug and categorized according to the Medical Dictionary for Regulatory Activities （MedDRA）.

Study contacts

Contact information is provided by the study sponsor or research team.

Qian Jia

CONTACT

[email protected]

028-88610620

Sponsors and collaborators

Lead sponsor

Chengdu Kangnuoxing Biopharma,Inc.

Industry

Registry information

Official study title

A Prospective Study of Stapokibart Injection in Patients With SAR

Important dates

Study start
2026
Primary completion
2027
Study completion
2028
First posted
Mar 9, 2026
Registry last updated
Mar 9, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.