Maralixibat for Intrahepatic Cholestasis of Pregnancy
Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexFemale
Age18-50
SponsorImperial College London
About this trial
An open label phase 2a/b trial of maralixibat in patients with Intrahepatic Cholestasis of Pregnancy (ICP) and elevated serum bile acid concentrations (sBA) to evaluate safety and tolerability
Eligibility criteria
Qualifiers
Provide signed informed consent and be willing to comply with all study visits and requirements through end of study, including the follow-up period
Female aged ≥18 and ≤50 years with a viable singleton pregnancy between 20 weeks 0 days and 34 weeks 0 days (inclusive) at the screening visit, and no more than 35 weeks 0 days (inclusive) at the baseline visit.
Diagnosis of ICP
Non fasting (e.g., postprandial) tSBA level ≥19 μmol/L as assessed by the local laboratory.
Disqualifiers
At the time of either the screening or baseline visit, decision has already been made to deliver within the next 7 days, for any indication.
Known non-reassuring fetal status based upon antepartum testing (e.g., NST/CTG) at or within 7 days before the baseline visit.
Known fetal anomaly likely to result in intrauterine fetal demise or neonatal death within the first 30 days of life.
Participating in another ongoing interventional clinical study at screening or planning to participate in another contemporaneous interventional clinical study while participating in this study.
Trial design
Treatments tested in this trial
- Maralixibat
Treatment groups
28 Participants
are divided into 1 treatment groupSponsors and collaborators
Imperial College London
Lead sponsor
Mirum Pharmaceuticals, Inc.
Collaborator
Source ClinicalTrials.gov