Phase 2 Pancreatitis Trial, Recruiting NCT03684278 Sponsor: University of Liverpool Condition: Pancreatitis
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Phase 2 Pancreatitis Trial, Recruiting

NCT03684278
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You are an adult who came to the Emergency Department or was admitted to hospital through a GP with a new diagnosis of acute pancreatitis (a sudden inflammation of the pancreas), confirmed by at least two of these three things: typical severe upper belly pain, a blood test showing raised pancreatic enzymes (amylase and/or lipase at least 3 times the normal level), or a CT or MRI scan showing signs of pancreatitis
  • The trial treatment can be started within 36 hours of you being admitted to hospital with this new diagnosis
  • You (or your legal representative, if you are unable to consent yourself) have agreed to take part and given written consent

Who may not be able to join:

  • You are under 18 or over 85 years old
  • You weigh more than 200 kg
  • You have had acute pancreatitis in the last 30 days, or you have long-term (chronic) pancreatitis
  • You have multiple sclerosis, systemic vasculitis, Guillain-Barré syndrome, or another condition affecting the nerve coverings (confirm with trial site)
  • You have a known history of epilepsy
  • You have moderate to severe heart failure or significant coronary (heart) disease
  • You have a serious lung condition, including cystic fibrosis, severe asthma, or severe COPD
  • You use oxygen at home or a breathing machine at home
  • You have yellowing of the skin or eyes (jaundice) or known advanced liver disease
  • You have a known cancer for which you are currently receiving, or have recently finished (within the last 6 months), chemotherapy or radiotherapy
  • You have a known cancer of the blood or bone marrow
  • You have a known cancer that is being managed with palliative (end-of-life) care
  • You have a known or suspected active infection, including COVID-19, at the time your pancreatitis began
  • You have a known history of tuberculosis (TB), or you live with someone who has TB, or you have had a serious opportunistic infection (an infection that occurs when the immune system is weakened)
  • You have a known history of hepatitis caused by infection (infective hepatitis)
  • You have a rare disease or inherited condition that significantly raises your risk of infections, such as severe combined immunodeficiency (SCID) or homozygous sickle cell disease
  • You have received a live vaccine or been given any infectious agent within the month before being admitted to hospital
  • You have taken immunosuppressant or biologic medicines within the month before being admitted to hospital
  • You have a known allergy or sensitivity to infliximab, any of its inactive ingredients, or any proteins derived from mice
  • You are known to be pregnant or breastfeeding at the time of admission
  • You are a woman who could become pregnant and are not willing to use reliable contraception for up to 6 months after receiving the trial treatment
  • You have taken part in another clinical drug trial within the last three months

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Robert Sutton, DPhil, FRCS, University of Liverpool

Phone: (0) 151 794 9774

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
University of Liverpool
Registry
ClinicalTrials.gov
Start date
1 May 2019
Est. completion
15 December 2026

Where this trial is recruiting

🇬🇧 United Kingdom

Primary endpoints

Difference in mean serum CRP measured on days 2, 4 and 14

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov