A Multicenter, Randomized, Double-blind, Placebo-controlled Study to Evaluate CBP-201 in Adult Patients with Chronic Rhinosinusitis with Nasal Polyps

  • sponsor
    Suzhou Connect Biopharmaceuticals Ltd.
Updated on 7 March 2022
nasal polyps


To evaluate the efficacy of CBP-201 in patients with chronic rhinosinusitis with nasal polyps 


To evaluate the efficacy of CBP-201 on a background of mometasone furoate nasal spray (MFNS) in reducing endoscopic NPS and nasal congestion/obstruction score (NCS) severity in patients with CRSwNP whose disease remains inadequately controlled despite daily treatment with intranasal corticosteroid (INCS) therapy in comparison to placebo.

Condition Sinusitis, Polyps
Clinical Study IdentifierTX291465
SponsorSuzhou Connect Biopharmaceuticals Ltd.
Last Modified on7 March 2022


Yes No Not Sure

Inclusion Criteria

Female and male patients aged > 18 and < 75 years at the time of screening

Exclusion Criteria

Intolerance to the investigational product
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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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