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
1881
mi
from 91732
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
1881
mi
from 91732
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
2277
mi
from 91732
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
2277
mi
from 91732
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
1528
mi
from 91732
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
1528
mi
from 91732
Iowa City, IA
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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
217
mi
from 91732
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
217
mi
from 91732
Las Vegas, NV
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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
70
mi
from 91732
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
70
mi
from 91732
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
53
mi
from 91732
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
53
mi
from 91732
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
1919
mi
from 91732
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
1919
mi
from 91732
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
1924
mi
from 91732
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
1924
mi
from 91732
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
960
mi
from 91732
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
960
mi
from 91732
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
1463
mi
from 91732
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
1463
mi
from 91732
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
2103
mi
from 91732
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
2103
mi
from 91732
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
2184
mi
from 91732
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
2184
mi
from 91732
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
1469
mi
from 91732
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
1469
mi
from 91732
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
2351
mi
from 91732
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
2351
mi
from 91732
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
1358
mi
from 91732
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
1358
mi
from 91732
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
552
mi
from 91732
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
552
mi
from 91732
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
1654
mi
from 91732
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
1654
mi
from 91732
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 91732
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 91732
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
1810
mi
from 91732
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
1810
mi
from 91732
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
1708
mi
from 91732
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
1708
mi
from 91732
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
2218
mi
from 91732
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
2218
mi
from 91732
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
1165
mi
from 91732
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
1165
mi
from 91732
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
1195
mi
from 91732
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
1195
mi
from 91732
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
1188
mi
from 91732
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
1188
mi
from 91732
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
1991
mi
from 91732
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
1991
mi
from 91732
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
1226
mi
from 91732
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
1226
mi
from 91732
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
358
mi
from 91732
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
358
mi
from 91732
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 91732
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 91732
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
36
mi
from 91732
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
36
mi
from 91732
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
2281
mi
from 91732
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
2281
mi
from 91732
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 91732
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 91732
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
2125
mi
from 91732
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
2125
mi
from 91732
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
1739
mi
from 91732
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
1739
mi
from 91732
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
1558
mi
from 91732
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
1558
mi
from 91732
Saint Charles, MO
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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
1301
mi
from 91732
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
1301
mi
from 91732
Omaha, NE
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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
2400
mi
from 91732
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
2400
mi
from 91732
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 91732
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 91732
Amherst, 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 91732
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 91732
Manhasset, 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
2355
mi
from 91732
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
2355
mi
from 91732
Allentown, PA
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
2208
mi
from 91732
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
2208
mi
from 91732
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
2277
mi
from 91732
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
2277
mi
from 91732
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
1524
mi
from 91732
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
1524
mi
from 91732
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
2406
mi
from 91732
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
2406
mi
from 91732
Basking Ridge, NJ
Click here to add this to my saved trials
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
2562
mi
from 91732
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
2562
mi
from 91732
Providence, RI
Click here to add this to my saved trials
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
2203
mi
from 91732
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
2203
mi
from 91732
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
2410
mi
from 91732
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
2410
mi
from 91732
New Brunswick, NJ
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
Alabama Clinical Therapeutics, Llc
1792
mi
from 91732
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
1792
mi
from 91732
Birmingham, AL
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
Precision Trials
346
mi
from 91732
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
346
mi
from 91732
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
281
mi
from 91732
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
281
mi
from 91732
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
2320
mi
from 91732
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
2320
mi
from 91732
Aventura, FL
Click here to add this to my saved trials