[Study Title]

[Study Description]

Overview

This Study Is Recruiting: [Phase Number]	Actual Start Date: [Date]	Estimated Completion Date: [Date]	Novartis Reference Number: [CCTL019E2202]
Condition: [Conditions]	Interventions: [Interventions]	Estimated Enrollment: [number of participants]	ClinicalTrials.gov Identifier: [NCT03568461]

This Study Is Recruiting: [Phase Number]	Actual Start Date: [Date]
Estimated Completion Date: [Date]	Novartis Reference Number: [CCTL019E2202]
Condition: [Conditions]	Interventions: [Interventions]
Estimated Enrollment: [number of participants]	ClinicalTrials.gov Identifier: [NCT03568461]

Study Goal

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All drugs are either investigational or being studied for (a) new use(s). Efficacy and safety have not been established. There is no guarantee that they will become commercially available for the use(s) under investigation.

Eligibility

Participants may be eligible to participate if they:

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If you're interested in this clinical study, your doctor can help evaluate whether you are eligible to participate. Ask your doctor if your medical history or other treatments you're receiving may conflict with the study protocol. If you meet the eligibility criteria and agree to participate in the study: You will be required to sign an informed consent form (ICF). The ICF contains information about the study, which your doctor can help explain to you before you sign. Your doctor will need to complete the necessary tests to see if you are eligible. As with all clinical trials, you have the right to leave the study at any time, for any reason.

Find a Trial Site Location

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Still Have a Question?

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To view eligibility requirements for this trial, arms and interventions, trial sites and study design, please click to visit this trial on www.clinicaltrials.gov.

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