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Carcinoid Syndrome Efficacy Study Featuring an Oral Daily Paltusotine Regimen

← catalyst calendar

NCT07087054 · readout ≤ 377 d

Sponsored by Crinetics Pharmaceuticals Inc. (industry) · CRNX — their whole pipeline →.

Phase
Phase 3
Status
Recruiting
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
141estimated
Sites
67
Countries
Argentina, Brazil, Chile +10

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2025-11-19actualWhen the study began enrolling
Primary completionAug 2027estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionJan 2030estimatedThe whole study's end, after follow-up
First posted2025-07-25actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-04actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Carcinoid Syndrome
  • Carcinoid
  • Carcinoid Tumor
  • Carcinoid Tumor of Ileum
  • Carcinoid Tumor of Cecum
  • Carcinoid Tumor of Liver
  • Carcinoid Tumor of Pancreas
  • Carcinoid Syndrome Diarrhea
  • Carcinoid Intestine Tumor

Interventions

  • Drug: Paltusotine
  • Drug: Placebo

Primary outcome

what the primary-completion date above is the date OF
Participants will record the number of flushing per day in a daily diary to assess the efficacy of paltusotine vs placebo in reducing flushing episodes.
measured Measured at Week 12

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