Clinical Research Trials Archive – Closed Trials

This is our archive of closed clinical trials, which means that they are no longer accepting new participants or have been concluded. Once a research facility has chosen to close the study, it is sorted into the GPS archive by indication. If you are interested in enrolling in a clinical trial, then please browse our list of active clinical studies.

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We've found
12,214
archived clinical trials in
Women's Studies

Atezolizumab and Bevacizumab in Treating Patients With Recurrent, Persistent, or Metastatic Cervical Cancer
A Phase 2 Study of Atezolizumab (MPDL3280A) in Combination With Bevacizumab in Patients With Recurrent, Persistent or Metastatic Cervical Cancer
Status: Enrolling
Updated:  12/31/1969
University of Kentucky, Markey Cancer Center
mi
from
Lexington, KY
Atezolizumab and Bevacizumab in Treating Patients With Recurrent, Persistent, or Metastatic Cervical Cancer
A Phase 2 Study of Atezolizumab (MPDL3280A) in Combination With Bevacizumab in Patients With Recurrent, Persistent or Metastatic Cervical Cancer
Status: Enrolling
Updated: 12/31/1969
University of Kentucky, Markey Cancer Center
mi
from
Lexington, KY
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Avelumab for People With Recurrent Respiratory Papillomatosis
A Phase II Study of Avelumab in Subjects With Recurrent Respiratory Papillomatosis
Status: Enrolling
Updated:  12/31/1969
National Institutes of Health Clinical Center
mi
from
Bethesda, MD
Avelumab for People With Recurrent Respiratory Papillomatosis
A Phase II Study of Avelumab in Subjects With Recurrent Respiratory Papillomatosis
Status: Enrolling
Updated: 12/31/1969
National Institutes of Health Clinical Center
mi
from
Bethesda, MD
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A Randomized Controlled Trial of Permanent vs Absorbable Suture for Uterosacral Ligament Suspension
A Randomized Controlled Trial of Permanent vs Absorbable Suture for Uterosacral Ligament Suspension
Status: Enrolling
Updated:  12/31/1969
University of Iowa Hospitals and Clinics
mi
from
Iowa City, IA
A Randomized Controlled Trial of Permanent vs Absorbable Suture for Uterosacral Ligament Suspension
A Randomized Controlled Trial of Permanent vs Absorbable Suture for Uterosacral Ligament Suspension
Status: Enrolling
Updated: 12/31/1969
University of Iowa Hospitals and Clinics
mi
from
Iowa City, IA
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Las Vegas, NV
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Las Vegas, NV
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Oceanside, CA
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Oceanside, CA
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Wildomar, CA
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Wildomar, CA
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Atlanta, GA
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Atlanta, GA
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Decatur, GA
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Decatur, GA
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Bellevue, WA
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Bellevue, WA
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Little Rock, AR
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Little Rock, AR
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Gainesville, FL
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Gainesville, FL
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Orlando, FL
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Orlando, FL
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Lake Charles, LA
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Lake Charles, LA
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
New York, NY
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
New York, NY
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Houston, TX
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Houston, TX
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Orem, UT
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Orem, UT
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
New Orleans, LA
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
New Orleans, LA
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
San Bernardino, CA
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
San Bernardino, CA
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Pensacola, FL
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Pensacola, FL
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Hoffman Estates, IL
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Hoffman Estates, IL
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Study Site
mi
from
Raleigh, NC
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Study Site
mi
from
Raleigh, NC
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Oklahoma City, OK
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Oklahoma City, OK
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Fort Worth, TX
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Fort Worth, TX
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage investigational Site
mi
from
San Antonio, TX
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage investigational Site
mi
from
San Antonio, TX
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Chapel Hill, NC
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Chapel Hill, NC
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Richardson, TX
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Richardson, TX
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Chandler, AZ
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Chandler, AZ
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Corona, CA
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Corona, CA
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Riverside, CA
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Riverside, CA
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Washington,
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Washington,
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Aventura, FL
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Aventura, FL
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Pinellas Park, FL
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Pinellas Park, FL
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Owensboro, KY
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Owensboro, KY
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Saint Charles, MO
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Saint Charles, MO
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Omaha, NE
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Omaha, NE
Click here to add this to my saved trials
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Princeton, NJ
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Princeton, NJ
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A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Amherst, NY
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Amherst, NY
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A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Manhasset, NY
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Manhasset, NY
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A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Allentown, PA
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Allentown, PA
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A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated:  12/31/1969
Sage Investigational Site
mi
from
Charlottesville, VA
A Study to Evaluate SAGE-217 in Subjects With Severe Postpartum Depression
A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy, Safety, and Pharmacokinetics of SAGE-217 in the Treatment of Adult Female Subjects With Severe Postpartum Depression
Status: Enrolling
Updated: 12/31/1969
Sage Investigational Site
mi
from
Charlottesville, VA
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Neurophysiologic Study of Patient With Essential Tremor and Dystonic Tremor
Neurophysiologic Study of Patients With Essential Tremor and Dystonic Tremor
Status: Enrolling
Updated:  12/31/1969
National Institutes of Health Clinical Center
mi
from
Bethesda, MD
Neurophysiologic Study of Patient With Essential Tremor and Dystonic Tremor
Neurophysiologic Study of Patients With Essential Tremor and Dystonic Tremor
Status: Enrolling
Updated: 12/31/1969
National Institutes of Health Clinical Center
mi
from
Bethesda, MD
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Evaluation of the Relationship Between Vaginal and Lower Urinary Tract Microbiomes and Infection After Hysterectomy
Evaluation of Vaginal and Urinary Microbiome Markers as Predictors of Post-Surgical Urinary Tract Infection
Status: Enrolling
Updated:  12/31/1969
Mayo Clinic Rochester
mi
from
Rochester, MN
Evaluation of the Relationship Between Vaginal and Lower Urinary Tract Microbiomes and Infection After Hysterectomy
Evaluation of Vaginal and Urinary Microbiome Markers as Predictors of Post-Surgical Urinary Tract Infection
Status: Enrolling
Updated: 12/31/1969
Mayo Clinic Rochester
mi
from
Rochester, MN
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Evaluation of the Impact of Reduced Oxygen Concentration on Embryonic Development
Evaluation of the Impact of Reduced Oxygen Concentration on Embryonic Development
Status: Enrolling
Updated:  12/31/1969
Reproductive Medicine Associates of New Jersey
mi
from
Basking Ridge, NJ
Evaluation of the Impact of Reduced Oxygen Concentration on Embryonic Development
Evaluation of the Impact of Reduced Oxygen Concentration on Embryonic Development
Status: Enrolling
Updated: 12/31/1969
Reproductive Medicine Associates of New Jersey
mi
from
Basking Ridge, NJ
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POCUS Assessment of Bladder Fullness for Girls Awaiting Radiology-Performed Transabdominal Pelvic Ultrasound
Point-of-Care-Ultrasound Assessment of Bladder Fullness for Girls Awaiting Radiology-Performed Transabdominal Pelvic Ultrasound: A Randomized Controlled Trial
Status: Enrolling
Updated:  12/31/1969
Hasbro Children's Hospital Emergency Department
mi
from
Providence, RI
POCUS Assessment of Bladder Fullness for Girls Awaiting Radiology-Performed Transabdominal Pelvic Ultrasound
Point-of-Care-Ultrasound Assessment of Bladder Fullness for Girls Awaiting Radiology-Performed Transabdominal Pelvic Ultrasound: A Randomized Controlled Trial
Status: Enrolling
Updated: 12/31/1969
Hasbro Children's Hospital Emergency Department
mi
from
Providence, RI
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Comparison of PIEB vs CEI for Labor Analgesia
Comparison of Programmed Intermittent Epidural Boluses With Continuous Epidural Infusion for Maintenance of Labor Analgesia
Status: Enrolling
Updated:  12/31/1969
Duke Univ Med Ctr
mi
from
Durham, NC
Comparison of PIEB vs CEI for Labor Analgesia
Comparison of Programmed Intermittent Epidural Boluses With Continuous Epidural Infusion for Maintenance of Labor Analgesia
Status: Enrolling
Updated: 12/31/1969
Duke Univ Med Ctr
mi
from
Durham, NC
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Acceptance and Commitment Therapy in Improving Well-Being in Patients With Stage III-IV Cancer and Their Partners
Couple-Focused ACT Intervention for Couples Coping With Cancer: A Pilot Study
Status: Enrolling
Updated:  12/31/1969
Rutgers Cancer Institute of New Jersey
mi
from
New Brunswick, NJ
Acceptance and Commitment Therapy in Improving Well-Being in Patients With Stage III-IV Cancer and Their Partners
Couple-Focused ACT Intervention for Couples Coping With Cancer: A Pilot Study
Status: Enrolling
Updated: 12/31/1969
Rutgers Cancer Institute of New Jersey
mi
from
New Brunswick, NJ
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Safety and Efficacy of Oral Encochleated Amphotericin B (CAMB/MAT2203) in the Treatment of Vulvovaginal Candidiasis (VVC)
A Multi-Center Randomized Study to Evaluate the Safety, Tolerability, and Efficacy of Oral Encochleated Amphotericin B (CAMB/MAT2203) Compared With Oral Fluconazole in the Treatment of Moderate to Severe Vulvovaginal Candidiasis (VVC)
Status: Enrolling
Updated:  12/31/1969
Alabama Clinical Therapeutics, Llc
mi
from
Birmingham, AL
Safety and Efficacy of Oral Encochleated Amphotericin B (CAMB/MAT2203) in the Treatment of Vulvovaginal Candidiasis (VVC)
A Multi-Center Randomized Study to Evaluate the Safety, Tolerability, and Efficacy of Oral Encochleated Amphotericin B (CAMB/MAT2203) Compared With Oral Fluconazole in the Treatment of Moderate to Severe Vulvovaginal Candidiasis (VVC)
Status: Enrolling
Updated: 12/31/1969
Alabama Clinical Therapeutics, Llc
mi
from
Birmingham, AL
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Safety and Efficacy of Oral Encochleated Amphotericin B (CAMB/MAT2203) in the Treatment of Vulvovaginal Candidiasis (VVC)
A Multi-Center Randomized Study to Evaluate the Safety, Tolerability, and Efficacy of Oral Encochleated Amphotericin B (CAMB/MAT2203) Compared With Oral Fluconazole in the Treatment of Moderate to Severe Vulvovaginal Candidiasis (VVC)
Status: Enrolling
Updated:  12/31/1969
Precision Trials
mi
from
Phoenix, AZ
Safety and Efficacy of Oral Encochleated Amphotericin B (CAMB/MAT2203) in the Treatment of Vulvovaginal Candidiasis (VVC)
A Multi-Center Randomized Study to Evaluate the Safety, Tolerability, and Efficacy of Oral Encochleated Amphotericin B (CAMB/MAT2203) Compared With Oral Fluconazole in the Treatment of Moderate to Severe Vulvovaginal Candidiasis (VVC)
Status: Enrolling
Updated: 12/31/1969
Precision Trials
mi
from
Phoenix, AZ
Click here to add this to my saved trials
Safety and Efficacy of Oral Encochleated Amphotericin B (CAMB/MAT2203) in the Treatment of Vulvovaginal Candidiasis (VVC)
A Multi-Center Randomized Study to Evaluate the Safety, Tolerability, and Efficacy of Oral Encochleated Amphotericin B (CAMB/MAT2203) Compared With Oral Fluconazole in the Treatment of Moderate to Severe Vulvovaginal Candidiasis (VVC)
Status: Enrolling
Updated:  12/31/1969
National Research Institute - Wilshire
mi
from
Los Angeles, CA
Safety and Efficacy of Oral Encochleated Amphotericin B (CAMB/MAT2203) in the Treatment of Vulvovaginal Candidiasis (VVC)
A Multi-Center Randomized Study to Evaluate the Safety, Tolerability, and Efficacy of Oral Encochleated Amphotericin B (CAMB/MAT2203) Compared With Oral Fluconazole in the Treatment of Moderate to Severe Vulvovaginal Candidiasis (VVC)
Status: Enrolling
Updated: 12/31/1969
National Research Institute - Wilshire
mi
from
Los Angeles, CA
Click here to add this to my saved trials
Safety and Efficacy of Oral Encochleated Amphotericin B (CAMB/MAT2203) in the Treatment of Vulvovaginal Candidiasis (VVC)
A Multi-Center Randomized Study to Evaluate the Safety, Tolerability, and Efficacy of Oral Encochleated Amphotericin B (CAMB/MAT2203) Compared With Oral Fluconazole in the Treatment of Moderate to Severe Vulvovaginal Candidiasis (VVC)
Status: Enrolling
Updated:  12/31/1969
South Florida Medical Research
mi
from
Aventura, FL
Safety and Efficacy of Oral Encochleated Amphotericin B (CAMB/MAT2203) in the Treatment of Vulvovaginal Candidiasis (VVC)
A Multi-Center Randomized Study to Evaluate the Safety, Tolerability, and Efficacy of Oral Encochleated Amphotericin B (CAMB/MAT2203) Compared With Oral Fluconazole in the Treatment of Moderate to Severe Vulvovaginal Candidiasis (VVC)
Status: Enrolling
Updated: 12/31/1969
South Florida Medical Research
mi
from
Aventura, FL
Click here to add this to my saved trials