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Completed Phase 2 Interventional Results available

A Study of Auxora in Patients With Acute Pancreatitis and Accompanying SIRS

ClinicalTrials.gov ID: NCT04681066

Public ClinicalTrials.gov record NCT04681066. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 30, 2026, 5:55 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-Blind, Placebo Controlled Dose-Ranging Study of Auxora in Patients With Acute Pancreatitis and Accompanying Systemic Inflammatory Response Syndrome

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Approximately 216 patients with acute pancreatitis and accompanying SIRS will be randomized at approximately 30 sites. Patients will be randomly assigned to either Auxora at one of three dose levels or one of three placebo volumes to maintain the double-blind. Study drug infusions will occur every 24 hours for three consecutive days for a total of three infusions. Patients will remain hospitalized as per standard of care and once discharged will be asked to complete a daily meal diary and return for a Day 30 safety assessment. It is recommended that patients randomized in the study should not be discharged from the hospital until solid food is tolerated, abdominal pain has resolved or been adequately controlled, and there is no clinical evidence of infection necessitating continued hospitalization.

Study identification

NCT ID
NCT04681066
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
CalciMedica, Inc.
Industry
Enrollment
216 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 24, 2021 (Actual)
Primary completion
May 15, 2024 (Actual)
Completion
May 15, 2024 (Actual)
Last update posted
Aug 24, 2026

2021 – 2024

United States locations

U.S. sites
27
U.S. states
16
U.S. cities
24
Facility City State ZIP Site status
Long Beach Medical Center Long Beach California 90806 —
LA County Hospital - USC Los Angeles California 90033 —
Cedars Sinai Los Angeles California 90048 —
University of California at Irvine Medical Center Orange California 92868 —
Harbor UCLA Medical Center Torrance California 90502 —
Torrance Memorial Medical Center Torrance California 90505 —
The Stamford Hospital Stamford Connecticut 06902 —
Sarasota Memorial Health Care System Sarasota Florida 34239 —
Tampa General Hospital Tampa Florida 33606 —
St. Luke's Regional Medical Center Boise Idaho 83712 —
Northwestern University Hospital Chicago Illinois 60611 —
Robley Rex VA Medical Center Louisville Kentucky 40206 —
University of Maryland Baltimore Maryland 21201 —
Henry Ford Health System Detroit Michigan 48202 —
Methodist Hospital Saint Louis Park Minnesota 55426 —
Regions Hospital Saint Paul Minnesota 55101 —
University of Missouri School of Medicine Columbia Missouri 65212 —
Washington University School of Medicine St Louis Missouri 63110 —
Northshore University Hospital Manhasset New York 11030 —
Icahn School of Medicine at Mount Sinai New York New York 10029 —
Ohio State University Columbus Ohio 43201 —
Regional One Health Memphis Tennessee 38106 —
John Peter Smith Hospital Fort Worth Texas 76104 —
Houston Methodist Hospital Houston Texas 77030 —
UT Health Houston Houston Texas 77030 —
University of Virginia Charlottesville Virginia 22908 —
CAMC Institute for Academic Medicine Charleston West Virginia 25304 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 10 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04681066, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 24, 2026 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04681066 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →