EligibleTrials

Carcinoid Syndrome Efficacy Study Featuring an Oral Daily Paltusotine Regimen

Recruiting · NCT07087054 · Interventional (participants receive a specific treatment) · Lead sponsor: Crinetics Pharmaceuticals Inc.

View the official record on ClinicalTrials.gov →
Pancreatic cancer

Interventions studied

PaltusotinePlacebo

What this trial is about

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.

Who can take part

Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Phase 3
Study type
Interventional (participants receive a specific treatment)

Inclusion criteria

Exclusion criteria

Where it is running

60 locations listed across 16 US states.

Showing 60 of 67 listed sites. See the official record for the complete list.

Read the full protocol, contacts and eligibility on ClinicalTrials.gov →

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