Phase IIb, Randomised, Double-blind, Placebo-controlled, Multi-centre Trial of Infliximab With Transcriptomic Biomarker and Mechanism Evaluation in Patients With Acute Pancreatitis.

Who is this study for? Patients with Acute Pancreatitis
What treatments are being studied? Infliximab
Status: Recruiting
Location: See all (13) locations...
Intervention Type: Drug, Other
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This study evaluates the effectiveness and safety of infliximab in the treatment of acute pancreatitis in adults. A third of participants will receive one single dose of infliximab via infusion, another third will receive a higher dose of infliximab via infusion and the final third of participants will receive a placebo infusion.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 85
Healthy Volunteers: f
View:

• Adult patients attending Accident and Emergency (A\&E) at or admitted to recruiting hospitals via a GP with a new diagnosis of AP established by two of the following three criteria: (1) typical continuous upper abdominal pain; (2) amylase and/or lipase three or more times the upper limit of normal; (3) characteristic findings on abdominal imaging (if undertaken urgently by CT or MRI)

• Patients in whom trial treatment can be started within 36 hours of admission to hospital with a new diagnosis of acute pancreatitis allowing 120 min for preparation of trial medication

• Patients from whom appropriate consent is obtained (from the patient or their legal representative).

Locations
Other Locations
United Kingdom
Aberdeen Royal Infirmary
RECRUITING
Aberdeen
University Hospital of Wales
NOT_YET_RECRUITING
Cardiff
Royal Devon and Exeter Hospital
NOT_YET_RECRUITING
Exeter
St James's University Hospital
NOT_YET_RECRUITING
Leeds
Aintree University Hospital
RECRUITING
Liverpool
Royal Liverpool University Hospital
RECRUITING
Liverpool
Charing Cross Hospital
SUSPENDED
London
St Mary's Hospital
SUSPENDED
London
University College London Hospital
RECRUITING
London
Queen's Medical Centre
RECRUITING
Nottingham
John Radcliffe Hospital
RECRUITING
Oxford
Royal Cornwall Hospital
NOT_YET_RECRUITING
Truro
Whiston Hospital
RECRUITING
Whiston
Contact Information
Primary
Matt Smyth, BSc
rapid.one@liverpool.ac.uk
(0) 151 794 9774
Backup
Catherine E Spowart, BSc
catherine.spowart@liverpool.ac.uk
(0) 151 794 9776
Time Frame
Start Date: 2019-05-01
Estimated Completion Date: 2027-03-31
Participants
Target number of participants: 290
Treatments
Active_comparator: Infusion of 5 mg/kg Infliximab
Infliximab (Remicade) to be administered as a one time intravenous infusion in 250 ml (500 ml if patient weighs over 100 kg) 0.9% sodium chloride solution over a period of 2 hours. Dosage calculated at 5 mg of Infliximab, per kg of patient body weight.
Active_comparator: Infusion of 10 mg/kg Infliximab
Infliximab (Remicade) to be administered as a one time intravenous infusion in 250 ml (500 ml if patient weighs over 100 kg) 0.9% sodium chloride solution over a period of 2 hours. Dosage calculated at 10 mg of Infliximab, per kg of patient body weight.
Placebo_comparator: 0.9% Sodium Chloride (Placebo)
250 ml (500 ml if patient weighs over 100 kg) 0.9% Sodium Chloride to be administered as a one time intravenous infusion over a period of 2 hours.
Sponsors
Collaborators: Merck Sharp & Dohme LLC, Medical Research Council, Liverpool University Hospitals NHS Foundation Trust, Bangor University, National Institute for Health Research, United Kingdom
Leads: University of Liverpool

This content was sourced from clinicaltrials.gov

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