CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 25 enrolled
Drug / intervention
octreotidedrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00463983
NCT00463983Phase 2Completed

Phase 2 Study of Long Acting Octreotide in Idiopathic Pulmonary Fibrosis

Institut National de la Santé Et de la Recherche Médicale, France·interventional·Posted Apr 20, 2007·Updated Mar 5, 2025

In Brief

A Phase 2 clinical trial evaluating octreotide for Idiopathic Pulmonary Fibrosis. Completed, enrolled 25 participants across 16 sites.

Detailed Summary

Octreotide is a somatostatin analog with a long half-life in vivo. Octreotide has interesting anti-inflammatory and anti-fibrotic properties in vitro and in vivo. Somatostatin receptors are increased and Octreotide uptake is increased in the lung in patients with idiopathic pulmonary fibrosis. Our hypothesis is that octreotide may slow the degradation of lung function in patients with IPF. In this proof of concept study, patients with IPF will receive an intramuscular injection of slow release octreotide (Sandostatin LP, 30 mg)every 4 weeks for 48 weeks. Lung function (FVC, DLCO), HRCT scores for fibrosis and ground glass, 6 minute walking test,quality of life and survival will be monitored.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesFrance
Collaborators--

Timeline

Phase 2CompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedApr 20, 2007
Enrollment StartOct 1, 2006
Primary CompletionJan 1, 2010
Study CompletionJan 1, 2012
TodayJul 2, 2026
Enrollment to primary: 3.3 yearsPosted 19.2 years ago

Interventions

octreotidedrug