Can a biologic injection shrink nasal polyps and clear stuffy noses?
NCT ID NCT07807826
First seen Sep 08, 2026 · Last updated Sep 09, 2026 · Updated 1 time
Summary
This phase 3 trial tests whether an experimental biologic called CM512 can reduce nasal polyps and ease congestion in people with chronic rhinosinusitis with nasal polyps. About 240 participants receive either CM512 or a placebo as a subcutaneous injection. Researchers measure changes in nasal polyp size and congestion scores over 24 weeks, along with quality of life and safety.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- CM512, an experimental biologic given as a subcutaneous injection
- What this could lead to
- If CM512 works, it could offer a new non-surgical option to shrink nasal polyps and relieve stuffiness, improving daily breathing and quality of life.
- What could go wrong
- This is an early-phase test in 240 people, so results may not apply to everyone. CM512 may cause side effects or fail to outperform 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
-
Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
-
About 240 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
-
Oct 2026
An estimate. Start dates often move.
- Expected to finish
-
Jul 2028
An estimate. End dates often move.
- Lead sponsor
-
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
-
18 to 75 years
- Sex
-
Anyone
- Healthy volunteers
-
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: * with chronic rhinosinusitis with nasal polyposis (CRSwNP) * Nasal Polyp Score (NPS) of ≥5 with a minimum score of 2 in each nasal cavity * Nasal Congestion Score of 2 or 3 at screening period, and at least 2 at baseline * Contraception Exclusion Criteria: * Not enough washing out period for previous therapy, e.g., less than 10 weeks or 5 half-lives (whichever is longer) for Interleukin (IL)-4 receptor alpha subunit antagonists, less than 8 weeks or 5 half-lives for systemic immunosuppressant, less than 6 months for sinus surgery (including polypectomy).With malignant or benign tumor of nasal cavity
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Chronic rhinosinusitis with nasal polyposis (CRSWNP) are added.
By submitting, you agree to our Terms of use
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.
-
The study's own enquiry address
This study publishes an address for enquiries. See it below .
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
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
Show contact details
Enter your email to view the contact information for this study.
By submitting, you agree to our Terms of use
Study contacts
-
Contact
Email: •••••@•••••
Locations
-
Beijing Tongren Hospital, CMU
Beijing, Beijing Municipality, China
Contact Email: •••••@•••••
Contact Email: •••••@•••••