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Brief Title: Real-world Evidence Study EvaLuating PAtient-Reported Outcomes With XERMELO
Official Title: An Observational Study to Evaluate the Real-world Experience of Patients Who Are Initiating Treatment With Telotristat Ethyl (XERMELO™)
Study ID: NCT03223428
Brief Summary: The primary objective of the study is to estimate the proportion of carcinoid syndrome (CS) patients who are satisfied with their overall symptom control, 6 months after initiating treatment with telotristat ethyl (XERMELO).
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
RTI-HS, Research Triangle Park, North Carolina, United States
Name: Lonnie Brent, PhD
Affiliation: TerSera Therapeutics
Role: STUDY_DIRECTOR