A PK/PD Study of CM4620-IE in Patients With Acute Pancreatitis

Status Completed

Clinical Trial Summary

This open-label study will evaluate the pharmacodynamic and pharmacokinetic profile of CM4620-IE in patients with acute pancreatitis. The first five (5) patients will receive ≤ 2.08 mg/kg of CM4620-IE by continuous IV infusion on Day 1. If necessary, up to an additional 4 patients may be treated at a different dose of CM4620-IE as determined by the obtained PK and PD data. The infusion of CM4620-IE will start within 12 hours from the time the patient or LAR provides informed consent.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03709342
Study type	Interventional
Source	CalciMedica, Inc.
Contact
Status	Completed
Phase	Phase 2
Start date	January 6, 2019
Completion date	June 7, 2019

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