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Clinical Trials in China / NCT06516302
Active, not recruiting Phase 3

A Study of GR1802 in Participants With Chronic Sinusitis With Nasal Polyps

NCT06516302 · tracked via the Priya Life Science China tracker
Sponsor
Genrix (Shanghai) Biopharmaceutical Co., Ltd.
Phase
Phase 3
Started
2024-09-19
Last updated
2026-03-03

Condition(s) studied

Chronic Rhinosinusitis With Nasal Polyps

Investigational drug(s) / intervention(s)

GR1802Placebo

GR1802: GR1802 will be administered SC.

Placebo: The placebo will be administered SC.

Study summary

The goal of this clinical trial is to learn if GR1802 works to treat severe chronic rhinosinusitis with nasal polyps (CRSwNP) in adults. It will also learn about the safety of GR1802. The main questions it aims to answer are:

1. Does GR1802 reduce the need for surgery and systemic corticosteroid use?
2. What medical problems do participants have when taking GR1802?

Researchers will compare GR1802 to a placebo (a look-alike substance that contains no drug) to see if GR1802 works to treat CRSwNP.

Participants will:

Take GR1802 or a placebo once every 2 weeks for 13months. Visit the clinic once every 2 weeks for checkups and tests. Keep a diary of their symptoms and the dosage and number of times they use mometasone furoate nasal spray.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Diagnosed as CRSwNP and treated with systemic glucocorticoid within 2 years before screening; and/or those who had undergone surgery for nasal polyps before screening. * An endoscopic bilateral NPS at screening/lead-in period and the baseline period of at least 5 out of a maximum score of 8 (with a minimum socre of 2 in each nasal cavity). * Nasal congestion/blockade/obstruction with moderate or severe symptom severity at at screening period (score 2 or 3 ) . * Willing to sign an informed consent, able to comply with clinic visits and study-related procedures as per protocol. Exclusion Criteria: * Biologic therapy within 5 half-lives or within 10 weeks before baseline. * Anti-IL-4Rα antibody before screening. * An experimental drug within 5 half-lives or 1 months before baseline. * Systemic immunosuppressant to treat inflammatory disease or autoimmune disease within 2 months or 5 half-lives before baseline. * Initiation of allergen immunotherapy within 3 months before screening. * Participants receiving leukotriene antagonist/modifier before screening unless on continous treatment for at least 30 days. * Participants with FEV1 50% or less of predicted normal were excluded. * Participants who have undergone any intranasal and/or sinus surgery within 6 months before screening. * Acute sinusitis or upper respiratory infection within a defined time period before screening. * A nasal cavity tumor (malignant or benign). * Evidence of fungal rhinosinusitis. * Presence of another diagnosis associated with nasal polyps (i.e., eosinophilic granulomatosis with polyangiitis, granulomatosis with polyangiitis, Young's syndrome, cystic fibrosis). * Rhinitis medicamentosa. * Nasal septal deviation occluding at least one nostril. * Antrochoanal polyps. * Pregnant or lactating woman.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Beijing Tongren Hospital, Capital Medical University Beijing China

More Genrix (Shanghai) Biopharmaceutical Co., Ltd. trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06516302 on ClinicalTrials.gov ↗ ← All trials in China