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New shot could shrink nasal polyps and ease breathing
NCT ID NCT07132827
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests an experimental injection called SHR-1905 in 280 adults with chronic sinusitis and nasal polyps. Participants must have moderate-to-severe symptoms despite standard nasal sprays. The goal is to see if the drug shrinks polyps and improves congestion over 24 weeks compared to a placebo.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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About 280 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Aug 2025
- Expected to finish
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Apr 2028
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 75 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Weight ≥40kg 2. Diagnosed with chronic rhinosinusitis with nasal polyps (CRSwNP). 3. Bilateral nasal polyps at screening and baseline, total NPS ≥5, ≥2 points for each nostril. 4. NCS ≥2 at screening and baseline. 5. SNOT-22≥30 at screening period and baseline. 6. Recorded persistent NP symptoms for over 4 weeks prior to screening. 7. Subjects received standard therapy with intranasal corticosteroids (INCS) prior to randomization. 8. NP surgery in the past and/or SCS use within 1 years before screening(or with contraindications/ intolerances). Exclusion Criteria: 1. Any comorbidities that may affect the efficacy evaluation of nasal polyps. 2. Any comorbidities except for asthma that may affect blood EOS levels. 3. Concomitant with immunodeficiency. 4. Concomitant with contraindications or not suitable for nasal endoscopy. 5. Uncontrolled hypertension and/or uncontrolled diabetes. 6. Concomitant with infection within 4 weeks prior to randomization. 7. Uncontrolled epistaxis within 4 weeks prior to randomization. 8. Major surgery performed within 3 months prior to randomization, or surgery planned during the study, or treatments that may affect evaluations according to investigators. 9. Parasitic infection within 6 months before randomization. 10. Sinus or intranasal surgery within 6 months prior to screening, or changes in the nasal walls caused by sinus or intranasal surgery that made NPS evaluation impossible. 11. Malignancies diagnosed within 5 years before randomization (except those with a low risk of metastasis or death). 12. Abnormalities of laboratory tests at screening or baseline. 13. Concomitant with active hepatitis B, positive hepatitis C virus antibodies, positive human immunodeficiency virus antibodies, or positive treponema pallidum antibodies. 14. Prolonged QTc interval or other clinically significant abnormal results of ECG at screening or baseline that may cause significant safety risks to subjects. 15. FEV1 before the use of bronchodilator (pre-BD) was less than 50% at screening. 16. Transfusion of blood products or immunoglobulin within 4 weeks prior to randomization. 17. SCS or additional INCS use within 4 weeks before randomization, or planned use during treatment period. 18. Regular use of decongestants (local or systemic) within 4 weeks before randomization, except for during the endoscopic procedure. 19. Adnimistration of live vaccine or viral vector vaccine within 4 weeks before randomization. 20. Allergen immunotherapy within 8 weeks before randomization. 21. Smoking at screening, or smoking cessation less than 6 months at screening. 22. Substance abuse, drug abuse, and/or excessive alcohol consumption within 1 year prior to randomization. Pregnancy (including positive pregnancy test at screening or baseline), lactation, or pregnancy plan during study period.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Eye & Ent Hospital of Fudan University
RECRUITINGShanghai, Shanghai Municipality, 200031, China
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Other studies related to the condition(s) this trial covers.
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- Can a new drug shrink nasal polyps and restore smell?
- Triple-Action nasal spray could ease chronic sinusitis