Pasireotide s.c. in patients with Post-Bariatric Hypoglycaemia
Research type
Research Study
Full title
A double-blind randomized placebo-controlled dose-finding phase II study to assess the efficacy and safety of pasireotide s.c. in patients with Post-Bariatric Hypoglycaemia
IRAS ID
1008341
Contact name
Raffaele Sabia
Contact email
Sponsor organisation
Recordati AG
Clinicaltrials.gov Identifier
Research summary
Phase II clinical study designed to find the best s.c. (subcutaneous, i.e. under the skin) Pasireotide dose to treat patients who have had a Bariatric surgery and Hypoglycaemia (low glucose levels), where neither the patient nor the doctor knows if active medicine or placebo (looks like a medicine but contains no active ingredient) is administered
REC name
North West - Greater Manchester South Research Ethics Committee
REC reference
24/NW/0030
Date of REC Opinion
18 Mar 2024
REC opinion
Further Information Favourable Opinion