Clinical trial

Lanreotide (Somatuline Autogel) in Thyroid-associated Ophthalmopathy Treatment

NCT00288522 · Ipsen, Industry · Terminated

Key facts

NCT number NCT00288522
Title Lanreotide (Somatuline Autogel) in Thyroid-associated Ophthalmopathy Treatment
Official title A Phase II, Single Centre, Randomized, Double-blind, Parallel and Placebo Controlled, Pilot Study to Evaluate the Efficacy and Safety of Somatuline Autogel 60mg in Patients With Active Thyroid-associated Ophthalmopathy of Moderate Intensity.
Lead sponsor Ipsen, Industry
Status Terminated
Phase Phase 2
Study type Interventional
Conditions Thyroid-Associated Ophthalmopathy
Intervention type Drug
Interventions Lanreotide (Autogel formulation). Duration of treatment - 3 injections, 1 every 28 days
Enrollment 5
Start date Jan 1, 2006
Primary completion Apr 1, 2007
Completion Apr 1, 2007
First posted Feb 8, 2006
Last update posted Jun 2, 2020
Countries Spain

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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