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Terminated Phase 2Phase 3 Interventional Results available

Study of the Efficacy and Safety of AMAG-423 (Digoxin Immune Fab) in Antepartum Subjects With Severe Preeclampsia

ClinicalTrials.gov ID: NCT03008616

Public ClinicalTrials.gov record NCT03008616. 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 Sep 4, 2026, 3:20 AM 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 Phase 2b/3a, Multi-Center, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study of the Efficacy and Safety of AMAG-423, a Digoxin Immune Fab, in Antepartum Subjects With Severe Preeclampsia

Brief summary

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

This study evaluates the use of AMAG-423 (Digoxin Immune Fab) in addition to expectant management in the treatment of severe preeclampsia as compared to placebo.

Study identification

NCT ID
NCT03008616
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
AMAG Pharmaceuticals, Inc.
Industry
Enrollment
58 participants

Conditions and interventions

Interventions

Biological · Other

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
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
Apr 11, 2017
Primary completion
Aug 12, 2020
Completion
Aug 12, 2020
Last update posted
May 21, 2026

2017 – 2020

United States locations

U.S. sites
16
U.S. states
12
U.S. cities
15
Facility City State ZIP Site status
University of South Alabama Mobile Alabama 36604
University of Kansas Medical Center Kansas City Kansas 66160
Children's Hospital Foundation Building Louisville Kentucky 40202
Louisiana State University Health Sciences Center in New Orleans New Orleans Louisiana 70112
University of Maryland Baltimore Maryland 21201
Detroit Medical Center (DMC) Detroit Michigan 48201
University Of Mississippi Medical Center Jackson Mississippi 39216
University of Cincinnati Medical Center Cincinnati Ohio 45219
University Hospitals Case Medical Center-Case Western Reserve University (CWRU) Cleveland Ohio 44106
Regional Obstetrical Consultants Chattanooga Tennessee 37403
The University of Texas Medical Branch (UTMB) Galveston Texas 77555
Texas Children's Hospital/Baylor College of Medicine Houston Texas 77030
The University of Texas Health Science Center at Houston (UTHSC-H) Houston Texas 77303
Baylor Scott & White Health Temple Texas 76508
University of Virginia School Of Medicine Charlottesville Virginia 29208
Medical College of Wisconsin Milwaukee Wisconsin 53226

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 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03008616, 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 May 21, 2026 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03008616 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →