Carcinoid Syndrome

3

Review clinical trials related to Carcinoid Syndrome. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Carcinoid Syndrome Efficacy Study Featuring an Oral Daily Paltusotine Regimen

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.

Participants needed: 141
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Crinetics Pharmaceuticals Inc.Updated: Jun 25, 2026Locations: 51
Eligibility criteria

Male or female ≥18 years of age, at the time of Screening. [+5]

Diarrhea attributed to any condition(s) other than carcinoid syndrome. [+11]

Status: Not yet recruiting

CardioNETPOL National Registry of Carcinoid Heart Disease

Carcinoid tumors are neuroendocrine tumors (NETs), most commonly originating from the gastrointestinal tract, that may secrete bioactive substances such as serotonin. Persistent exposure to these mediators can lead to carcinoid syndrome and, in up to 50% of patients, carcinoid heart disease (CHD). CHD is characterized by fibrotic degeneration of cardiac valves, predominantly right-sided, resulting in progressive valvular dysfunction and a significant increase in mortality. The mechanisms underlying selective cardiac involvement and predictors of disease progression remain incompletely understood. In addition, optimal timing and selection of surgical versus transcatheter valve interventions, particularly in high-risk patients, require further clarification. This multicenter, retrospective observational registry aims to identify and characterize patients with carcinoid heart disease and at least moderate valvular involvement. CHD is defined by confirmed neuroendocrine tumor, echocardiographic evidence of ≥ moderate valvular disease with features of fibrosis, elevated NT-proBNP (\>260 ng/L), and histopathological confirmation when available. Approximately 100-120 consecutive patients will be enrolled over 12 months. Standardized data collection will include detailed echocardiographic assessment, demographic and clinical characteristics, cardiovascular risk factors, comorbidities, tumor features, oncological treatment history, and cardiac management strategies. The primary objective is to describe the clinical profile and management of patients with CHD in a real-world multicenter setting. Secondary objectives include identifying factors associated with advanced valvular dysfunction and evaluating eligibility and outcomes of transcatheter valve therapies. The registry is expected to improve risk stratification and support clinical decision-making in carcinoid heart disease.

Participants needed: 120
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: National Institute of Cardiology, Warsaw, PolandUpdated: Mar 4, 2026Locations: 1
Eligibility criteria

Age ≥ 18 years. [+6]

Patients with insufficient clinical or imaging data to confirm carcinoid heart d... [+3]

Status: Recruiting

Fibrosis in Chronic and Delayed Myocardial Infarction

In this study the investigators aim to examine the role that fibrosis plays in heart conditions such as aortic stenosis , chemotherapy-induced cardiotoxicity and carcinoid syndrome . Fibrosis is a common final result following any injury to the heart muscle and the investigators aim to identify this process early and in its active state. This will be examined by using a radiotracer 68Ga-FAPI or 18F-AlF-FAPI and PET-MRI or PET-CT.

Participants needed: 180
Trial details
Age: 40-90Biological sex: AllType: ObservationalSponsor: University of EdinburghUpdated: Jan 9, 2026Locations: 1
Eligibility criteria

Male or female above the age of 50 years old [+12]

Inability or unwilling to give informed consent. [+6]