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Study identifier: NCT07087054 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Carcinoid Syndrome Efficacy Study Featuring an Oral Daily Paltusotine Regimen

Condition: Carcinoid Syndrome · Carcinoid · Carcinoid Tumor  ·  Sponsor: Crinetics Pharmaceuticals Inc.

PhasePhase 3
Planned participants141
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

A Phase 3, randomized, double-blinded, placebo-controlled study to evaluate the efficacy and safety of paltusotine treatment vs placebo as well as the long-term safety of paltusotine in adults with carcinoid syndrome due to well-differentiated neuroendocrine tumors. The purpose of this study is to continue the evaluation of the safety, efficacy, and pharmacokinetics (PK) of paltusotine in participants with carcinoid syndrome.

This description comes directly from the study's public registry record.

Talk to the study team

Crinetics Clinical Trials  ·  833-276-4636  ·  clinicaltrials@crinetics.com

Always discuss trial participation with your own doctor first.

Locations (51)

Banner MD Anderson Cancer CenterGilbert, Arizona, United StatesRecruiting
Hoag Memorial Hospital PresbyterianNewport Beach, California, United StatesRecruiting
Yale University - New Haven Hospital - Yale Cancer CenterNew Haven, Connecticut, United StatesRecruiting
University of MiamiMiami, Florida, United StatesRecruiting
Moffitt Cancer CenterTampa, Florida, United StatesRecruiting
Winshop Cancer Institute - Emory UniversityAtlanta, Georgia, United StatesRecruiting
University of Iowa Health CareIowa City, Iowa, United StatesRecruiting
University of Kentucky Medical CenterLexington, Kentucky, United StatesRecruiting
Louisiana State University Health SciencesMetairie, Louisiana, United StatesRecruiting
Henry Ford Cancer - DetroitDetroit, Michigan, United StatesRecruiting
Mayo ClinicRochester, Minnesota, United StatesRecruiting
Icahn School of Medicine at Mount SinaiNew York, New York, United StatesRecruiting

+ 39 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07087054