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

PHASE2/PHASE3TerminatedINTERVENTIONAL
Enrollment

59

Participants

Timeline

Start Date

April 12, 2017

Primary Completion Date

August 13, 2020

Study Completion Date

August 13, 2020

Conditions
Severe Preeclampsia
Interventions
BIOLOGICAL

AMAG-423 (digoxin immune fab)

AMAG-423 (digoxin immune fab) 3.2 mg/kg, 30 minute IV infusion, every 6 hours x 4 days

OTHER

Placebo

Normal saline, 30 minute IV infusion, every 6 hours x 4 days

Trial Locations (18)

21201

University of Maryland, Baltimore

29208

University of Virginia School Of Medicine, Charlottesville

36604

University of South Alabama, Mobile

37403

Regional Obstetrical Consultants, Chattanooga

39216

University Of Mississippi Medical Center, Jackson

40202

Children's Hospital Foundation Building, Louisville

44106

University Hospitals Case Medical Center-Case Western Reserve University (CWRU), Cleveland

45219

University of Cincinnati Medical Center, Cincinnati

48201

Detroit Medical Center (DMC), Detroit

53226

Medical College of Wisconsin, Milwaukee

66160

University of Kansas Medical Center, Kansas City

70112

Louisiana State University Health Sciences Center in New Orleans, New Orleans

76508

Baylor Scott & White Health, Temple

77030

Texas Children's Hospital/Baylor College of Medicine, Houston

77303

The University of Texas Health Science Center at Houston (UTHSC-H), Houston

77555

The University of Texas Medical Branch (UTMB), Galveston

80-462

Adalbertus Hospital, Gdansk

0204

Sefako Makgatho Health Sciences University, Pretoria

Sponsors
All Listed Sponsors
lead

AMAG Pharmaceuticals, Inc.

INDUSTRY