A phase II proof of concept study to evalute the efficacy and safety of deep subcutaneous lanreotide Autogel 120 mg / 28 days on symptoms and healing of the esophageal and gastric mucosa in patients with gastro esophageal reflux resitant to standard therapy (combination of proton pump inhibitors and H2 antagonists)
Latest Information Update: 07 Aug 2024
At a glance
- Drugs Lanreotide (Primary)
- Indications Gastro-oesophageal reflux
- Focus Proof of concept; Therapeutic Use
- 07 Aug 2024 Status changed from recruiting to completed.
- 12 Sep 2014 New trial record