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Global Clinical Development - General Medicine QAW039/fevipiprantClinical Trial protocol CQAW039A2316 / NCT03215758A 12-week, multicenter, randomized, double-blind, placebo-controlled study to assess the efficacy and safety of QAW039 when added to standard-of-care asthma therapy in patients with uncontrolled asthmaDocument type: Clinical Trial ProtocolEUDRACT number:2017-001273-16Version number:00 (OriginalProtocol) Clinical trial phase:IIIRelease date:10- May-2017Property of NovartisConfidentialMay not be used, divulged, published, or otherwise disclosedwithout the consent of NovartisClinical Trial protocol template Version (July 2016)NovartisConfidentialPage 2Clinical Trial protocol (Version 00) protocol No.

Enrollment Point/time of patient entry into the study at which informed consent must be obtained (e.g. prior to starting any of the procedures described in the protocol) Epoch/Period A portion of the study which serves a specific purpose. Typical epoch/periods are: screening/recruitment, wash-out, treatment, and follow-up

  Consent, Informed, Informed consent

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