For Healthcare Professionals

Regulatory Post-Marketing Surveillance of Xolair® for Chronic Rhinosinusitis With Nasal Polyps

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About the study

This study aims to evaluate the safety and effectiveness of Xolair® in patients with chronic rhinosinusitis with nasal polyps in routine clinical practice.
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Inclusion Criteria:


  1. Adults aged ≥18 years
  2. Patients with CRSwNP who are not adequately controlled with conventional therapy (INCS)
  3. Patients prescribed with Xolair® as per the locally approved label information.
  4. Patients who provide written informed consent to participate in the study

EXCLUSION CRITERIA

Exclusion Criteria:


  1. Patients who do not provide consent to participate in the study
  2. Patients participating in other clinical trial
  3. Contraindications listed in the locally approved label information of Xolair®

  1. Hypersensitivity to the active ingredient or any other ingredient of Xolair®
  2. Patients with myocardial infarction or history of myocardial infarction (pre-filled syringes only)

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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.
Phone iconCall +41613241111Email iconEmail Study Center

Study Details


Contition

Chronic Rhinosinusitis With Nasal Polyps

Age

18 - 100

Participants Needed

112

Est. Completion Date

Jan 31, 2025

Treatment Type

OBSERVATIONAL


Sponsor

Novartis

ClinicalTrials.gov NCT Identifier

NCT05626257

Study Number

CIGE025EKR04

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