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

Vaginal Tactile Imaging for Pelvic Floor Prolapse
Vaginal Tactile Imaging in Assessment of Pelvic Floor Conditions
Status: Enrolling
Updated:  12/31/1969
444
mi
from 43215
Princeton, NJ
Vaginal Tactile Imaging for Pelvic Floor Prolapse
Vaginal Tactile Imaging in Assessment of Pelvic Floor Conditions
Status: Enrolling
Updated: 12/31/1969
Princeton Urogynecology PU
444
mi
from 43215
Princeton, NJ
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Vaginal Tactile Imaging for Pelvic Floor Prolapse
Vaginal Tactile Imaging in Assessment of Pelvic Floor Conditions
Status: Enrolling
Updated:  12/31/1969
400
mi
from 43215
Allentown, PA
Vaginal Tactile Imaging for Pelvic Floor Prolapse
Vaginal Tactile Imaging in Assessment of Pelvic Floor Conditions
Status: Enrolling
Updated: 12/31/1969
Institute for Female Pelvic Medicine and Reconstructive Surgery
400
mi
from 43215
Allentown, PA
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Vaginal Tactile Imaging for Pelvic Floor Prolapse
Vaginal Tactile Imaging in Assessment of Pelvic Floor Conditions
Status: Enrolling
Updated:  12/31/1969
318
mi
from 43215
Falls Church, VA
Vaginal Tactile Imaging for Pelvic Floor Prolapse
Vaginal Tactile Imaging in Assessment of Pelvic Floor Conditions
Status: Enrolling
Updated: 12/31/1969
Inova Health System Foundation
318
mi
from 43215
Falls Church, VA
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Vaginal Tactile Imaging for Pelvic Floor Prolapse
Vaginal Tactile Imaging in Assessment of Pelvic Floor Conditions
Status: Enrolling
Updated:  12/31/1969
422
mi
from 43215
Norfolk, VA
Vaginal Tactile Imaging for Pelvic Floor Prolapse
Vaginal Tactile Imaging in Assessment of Pelvic Floor Conditions
Status: Enrolling
Updated: 12/31/1969
Eastern Virginia Medical School
422
mi
from 43215
Norfolk, VA
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Nivolumab or Expectant Observation Following Ipilimumab, Nivolumab, and Surgery in Treating Patients With High Risk Localized, Locoregionally Advanced, or Recurrent Mucosal Melanoma
A Randomized Phase II Trial of Adjuvant Nivolumab or Expectant Observation Following Neoadjuvant Ipilimumab Plus Nivolumab and Surgical Resection of High-Risk Localized, Locoregionally Advanced, or Recurrent Mucosal Melanoma
Status: Enrolling
Updated:  12/31/1969
641
mi
from 43215
Boston, MA
Nivolumab or Expectant Observation Following Ipilimumab, Nivolumab, and Surgery in Treating Patients With High Risk Localized, Locoregionally Advanced, or Recurrent Mucosal Melanoma
A Randomized Phase II Trial of Adjuvant Nivolumab or Expectant Observation Following Neoadjuvant Ipilimumab Plus Nivolumab and Surgical Resection of High-Risk Localized, Locoregionally Advanced, or Recurrent Mucosal Melanoma
Status: Enrolling
Updated: 12/31/1969
Alliance for Clinical Trials in Oncology
641
mi
from 43215
Boston, MA
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Counseling for Prematurity Using a Multimedia Education Tool
Effectiveness of Prenatal Counseling for Prematurity Using a Supplementary Multimedia Parent Education Tool
Status: Enrolling
Updated:  12/31/1969
335
mi
from 43215
Milwaukee, WI
Counseling for Prematurity Using a Multimedia Education Tool
Effectiveness of Prenatal Counseling for Prematurity Using a Supplementary Multimedia Parent Education Tool
Status: Enrolling
Updated: 12/31/1969
Froedtert Hospital
335
mi
from 43215
Milwaukee, WI
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Oxygen for Intrauterine Resuscitation of Category II Fetal Heart Tracings
Oxygen for Category II Intrauterine Fetal Resuscitation: A Randomized, Noninferiority Trial
Status: Enrolling
Updated:  12/31/1969
397
mi
from 43215
Saint Louis, MO
Oxygen for Intrauterine Resuscitation of Category II Fetal Heart Tracings
Oxygen for Category II Intrauterine Fetal Resuscitation: A Randomized, Noninferiority Trial
Status: Enrolling
Updated: 12/31/1969
Barnes Jewish Hospital
397
mi
from 43215
Saint Louis, MO
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Goals for Reaching Optimum Wellness (GROWell)
Goals for Reaching Optimum Wellness (GROWell): A Pilot Study of a Dietary Intervention During Pregnancy
Status: Enrolling
Updated:  12/31/1969
352
mi
from 43215
Durham, NC
Goals for Reaching Optimum Wellness (GROWell)
Goals for Reaching Optimum Wellness (GROWell): A Pilot Study of a Dietary Intervention During Pregnancy
Status: Enrolling
Updated: 12/31/1969
Duke Univ Med Ctr
352
mi
from 43215
Durham, NC
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Study of Topical ABI-1968 in Subjects With Precancerous Anal Lesions Resulting From Human Papillomavirus (HPV) Infection
Open-Label Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Single and Multiple Doses of Topical ABI-1968 in Subjects With Anal High-Grade Squamous Intraepithelial Lesions (aHSIL)
Status: Enrolling
Updated:  12/31/1969
2107
mi
from 43215
San Francisco, CA
Study of Topical ABI-1968 in Subjects With Precancerous Anal Lesions Resulting From Human Papillomavirus (HPV) Infection
Open-Label Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Single and Multiple Doses of Topical ABI-1968 in Subjects With Anal High-Grade Squamous Intraepithelial Lesions (aHSIL)
Status: Enrolling
Updated: 12/31/1969
Research Center
2107
mi
from 43215
San Francisco, CA
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Study of Topical ABI-1968 in Subjects With Precancerous Anal Lesions Resulting From Human Papillomavirus (HPV) Infection
Open-Label Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Single and Multiple Doses of Topical ABI-1968 in Subjects With Anal High-Grade Squamous Intraepithelial Lesions (aHSIL)
Status: Enrolling
Updated:  12/31/1969
793
mi
from 43215
Orlando, FL
Study of Topical ABI-1968 in Subjects With Precancerous Anal Lesions Resulting From Human Papillomavirus (HPV) Infection
Open-Label Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Single and Multiple Doses of Topical ABI-1968 in Subjects With Anal High-Grade Squamous Intraepithelial Lesions (aHSIL)
Status: Enrolling
Updated: 12/31/1969
Research Center
793
mi
from 43215
Orlando, FL
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Study of Topical ABI-1968 in Subjects With Precancerous Anal Lesions Resulting From Human Papillomavirus (HPV) Infection
Open-Label Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Single and Multiple Doses of Topical ABI-1968 in Subjects With Anal High-Grade Squamous Intraepithelial Lesions (aHSIL)
Status: Enrolling
Updated:  12/31/1969
276
mi
from 43215
Chicago, IL
Study of Topical ABI-1968 in Subjects With Precancerous Anal Lesions Resulting From Human Papillomavirus (HPV) Infection
Open-Label Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Single and Multiple Doses of Topical ABI-1968 in Subjects With Anal High-Grade Squamous Intraepithelial Lesions (aHSIL)
Status: Enrolling
Updated: 12/31/1969
Research Center
276
mi
from 43215
Chicago, IL
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Study of Topical ABI-1968 in Subjects With Precancerous Anal Lesions Resulting From Human Papillomavirus (HPV) Infection
Open-Label Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Single and Multiple Doses of Topical ABI-1968 in Subjects With Anal High-Grade Squamous Intraepithelial Lesions (aHSIL)
Status: Enrolling
Updated:  12/31/1969
9456
mi
from 43215
Sydney,
Study of Topical ABI-1968 in Subjects With Precancerous Anal Lesions Resulting From Human Papillomavirus (HPV) Infection
Open-Label Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Single and Multiple Doses of Topical ABI-1968 in Subjects With Anal High-Grade Squamous Intraepithelial Lesions (aHSIL)
Status: Enrolling
Updated: 12/31/1969
Research Center
9456
mi
from 43215
Sydney,
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Study of Topical ABI-1968 in Subjects With Precancerous Anal Lesions Resulting From Human Papillomavirus (HPV) Infection
Open-Label Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Single and Multiple Doses of Topical ABI-1968 in Subjects With Anal High-Grade Squamous Intraepithelial Lesions (aHSIL)
Status: Enrolling
Updated:  12/31/1969
483
mi
from 43215
New York, NY
Study of Topical ABI-1968 in Subjects With Precancerous Anal Lesions Resulting From Human Papillomavirus (HPV) Infection
Open-Label Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Single and Multiple Doses of Topical ABI-1968 in Subjects With Anal High-Grade Squamous Intraepithelial Lesions (aHSIL)
Status: Enrolling
Updated: 12/31/1969
Research Center
483
mi
from 43215
New York, NY
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Study of Topical ABI-1968 in Subjects With Precancerous Anal Lesions Resulting From Human Papillomavirus (HPV) Infection
Open-Label Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Single and Multiple Doses of Topical ABI-1968 in Subjects With Anal High-Grade Squamous Intraepithelial Lesions (aHSIL)
Status: Enrolling
Updated:  12/31/1969
307
mi
from 43215
Winston-Salem, NC
Study of Topical ABI-1968 in Subjects With Precancerous Anal Lesions Resulting From Human Papillomavirus (HPV) Infection
Open-Label Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Single and Multiple Doses of Topical ABI-1968 in Subjects With Anal High-Grade Squamous Intraepithelial Lesions (aHSIL)
Status: Enrolling
Updated: 12/31/1969
Research Center
307
mi
from 43215
Winston-Salem, NC
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Prescribing Exercise as Medicine in Pregnancy
Prescribing Exercise as Medicine in Pregnancy: A Randomized Controlled Trial
Status: Enrolling
Updated:  12/31/1969
400
mi
from 43215
Saint Louis, MO
Prescribing Exercise as Medicine in Pregnancy
Prescribing Exercise as Medicine in Pregnancy: A Randomized Controlled Trial
Status: Enrolling
Updated: 12/31/1969
St. Mary's Health Center
400
mi
from 43215
Saint Louis, MO
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Study of Topical ABI-1968 in Subjects With Precancerous Cervical Lesions From Human Papillomavirus (HPV) Infection
A Randomised, Double-Blind, Placebo-Controlled, Multiple-Dose Study to Evaluate Safety, Tolerability and Pharmacokinetics of Topical ABI-1968 in Subjects With Cervical High Grade Squamous Intreaepithelial Lesions (cHSIL)
Status: Enrolling
Updated:  12/31/1969
355
mi
from 43215
Chapel Hill, NC
Study of Topical ABI-1968 in Subjects With Precancerous Cervical Lesions From Human Papillomavirus (HPV) Infection
A Randomised, Double-Blind, Placebo-Controlled, Multiple-Dose Study to Evaluate Safety, Tolerability and Pharmacokinetics of Topical ABI-1968 in Subjects With Cervical High Grade Squamous Intreaepithelial Lesions (cHSIL)
Status: Enrolling
Updated: 12/31/1969
Research Center
355
mi
from 43215
Chapel Hill, NC
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Study of Topical ABI-1968 in Subjects With Precancerous Cervical Lesions From Human Papillomavirus (HPV) Infection
A Randomised, Double-Blind, Placebo-Controlled, Multiple-Dose Study to Evaluate Safety, Tolerability and Pharmacokinetics of Topical ABI-1968 in Subjects With Cervical High Grade Squamous Intreaepithelial Lesions (cHSIL)
Status: Enrolling
Updated:  12/31/1969
307
mi
from 43215
Winston-Salem, NC
Study of Topical ABI-1968 in Subjects With Precancerous Cervical Lesions From Human Papillomavirus (HPV) Infection
A Randomised, Double-Blind, Placebo-Controlled, Multiple-Dose Study to Evaluate Safety, Tolerability and Pharmacokinetics of Topical ABI-1968 in Subjects With Cervical High Grade Squamous Intreaepithelial Lesions (cHSIL)
Status: Enrolling
Updated: 12/31/1969
Research Center
307
mi
from 43215
Winston-Salem, NC
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Study of Topical ABI-1968 in Subjects With Precancerous Cervical Lesions From Human Papillomavirus (HPV) Infection
A Randomised, Double-Blind, Placebo-Controlled, Multiple-Dose Study to Evaluate Safety, Tolerability and Pharmacokinetics of Topical ABI-1968 in Subjects With Cervical High Grade Squamous Intreaepithelial Lesions (cHSIL)
Status: Enrolling
Updated:  12/31/1969
937
mi
from 43215
Lake Worth, FL
Study of Topical ABI-1968 in Subjects With Precancerous Cervical Lesions From Human Papillomavirus (HPV) Infection
A Randomised, Double-Blind, Placebo-Controlled, Multiple-Dose Study to Evaluate Safety, Tolerability and Pharmacokinetics of Topical ABI-1968 in Subjects With Cervical High Grade Squamous Intreaepithelial Lesions (cHSIL)
Status: Enrolling
Updated: 12/31/1969
Research Center
937
mi
from 43215
Lake Worth, FL
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Study of Topical ABI-1968 in Subjects With Precancerous Cervical Lesions From Human Papillomavirus (HPV) Infection
A Randomised, Double-Blind, Placebo-Controlled, Multiple-Dose Study to Evaluate Safety, Tolerability and Pharmacokinetics of Topical ABI-1968 in Subjects With Cervical High Grade Squamous Intreaepithelial Lesions (cHSIL)
Status: Enrolling
Updated:  12/31/1969
1508
mi
from 43215
Idaho Falls, ID
Study of Topical ABI-1968 in Subjects With Precancerous Cervical Lesions From Human Papillomavirus (HPV) Infection
A Randomised, Double-Blind, Placebo-Controlled, Multiple-Dose Study to Evaluate Safety, Tolerability and Pharmacokinetics of Topical ABI-1968 in Subjects With Cervical High Grade Squamous Intreaepithelial Lesions (cHSIL)
Status: Enrolling
Updated: 12/31/1969
Research Center
1508
mi
from 43215
Idaho Falls, ID
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Study of Topical ABI-1968 in Subjects With Precancerous Cervical Lesions From Human Papillomavirus (HPV) Infection
A Randomised, Double-Blind, Placebo-Controlled, Multiple-Dose Study to Evaluate Safety, Tolerability and Pharmacokinetics of Topical ABI-1968 in Subjects With Cervical High Grade Squamous Intreaepithelial Lesions (cHSIL)
Status: Enrolling
Updated:  12/31/1969
1975
mi
from 43215
Los Angeles, CA
Study of Topical ABI-1968 in Subjects With Precancerous Cervical Lesions From Human Papillomavirus (HPV) Infection
A Randomised, Double-Blind, Placebo-Controlled, Multiple-Dose Study to Evaluate Safety, Tolerability and Pharmacokinetics of Topical ABI-1968 in Subjects With Cervical High Grade Squamous Intreaepithelial Lesions (cHSIL)
Status: Enrolling
Updated: 12/31/1969
Research Center
1975
mi
from 43215
Los Angeles, CA
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Study of Topical ABI-1968 in Subjects With Precancerous Cervical Lesions From Human Papillomavirus (HPV) Infection
A Randomised, Double-Blind, Placebo-Controlled, Multiple-Dose Study to Evaluate Safety, Tolerability and Pharmacokinetics of Topical ABI-1968 in Subjects With Cervical High Grade Squamous Intreaepithelial Lesions (cHSIL)
Status: Enrolling
Updated:  12/31/1969
423
mi
from 43215
Norfolk, VA
Study of Topical ABI-1968 in Subjects With Precancerous Cervical Lesions From Human Papillomavirus (HPV) Infection
A Randomised, Double-Blind, Placebo-Controlled, Multiple-Dose Study to Evaluate Safety, Tolerability and Pharmacokinetics of Topical ABI-1968 in Subjects With Cervical High Grade Squamous Intreaepithelial Lesions (cHSIL)
Status: Enrolling
Updated: 12/31/1969
Research Center
423
mi
from 43215
Norfolk, VA
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Study of Topical ABI-1968 in Subjects With Precancerous Cervical Lesions From Human Papillomavirus (HPV) Infection
A Randomised, Double-Blind, Placebo-Controlled, Multiple-Dose Study to Evaluate Safety, Tolerability and Pharmacokinetics of Topical ABI-1968 in Subjects With Cervical High Grade Squamous Intreaepithelial Lesions (cHSIL)
Status: Enrolling
Updated:  12/31/1969
mi
from 43215
South Brisbane,
Study of Topical ABI-1968 in Subjects With Precancerous Cervical Lesions From Human Papillomavirus (HPV) Infection
A Randomised, Double-Blind, Placebo-Controlled, Multiple-Dose Study to Evaluate Safety, Tolerability and Pharmacokinetics of Topical ABI-1968 in Subjects With Cervical High Grade Squamous Intreaepithelial Lesions (cHSIL)
Status: Enrolling
Updated: 12/31/1969
Research Center
mi
from 43215
South Brisbane,
Click here to add this to my saved trials
A Study of Carboplatin and Paclitaxel Chemotherapy With Nivolumab in Patients With Ovarian Cancer
A Pilot Study of Nivolumab in Combination With Front-Line Neoadjuvant Dose Dense Paclitaxel and Carboplatin Chemotherapy and Post-Surgical Dose Dense Paclitaxel and Carboplatin Chemotherapy in Patients With High Grade Serous Ovarian, Fallopian Tube, or Primary Peritoneal Cancer
Status: Enrolling
Updated:  12/31/1969
480
mi
from 43215
New York, NY
A Study of Carboplatin and Paclitaxel Chemotherapy With Nivolumab in Patients With Ovarian Cancer
A Pilot Study of Nivolumab in Combination With Front-Line Neoadjuvant Dose Dense Paclitaxel and Carboplatin Chemotherapy and Post-Surgical Dose Dense Paclitaxel and Carboplatin Chemotherapy in Patients With High Grade Serous Ovarian, Fallopian Tube, or Primary Peritoneal Cancer
Status: Enrolling
Updated: 12/31/1969
Memorial Sloan Kettering Cancer Center
480
mi
from 43215
New York, NY
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An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated:  12/31/1969
1654
mi
from 43215
Phoenix, AZ
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated: 12/31/1969
Precision Trials AZ
1654
mi
from 43215
Phoenix, AZ
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An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated:  12/31/1969
1951
mi
from 43215
San Diego, CA
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated: 12/31/1969
Women's Health Care Research Corp.
1951
mi
from 43215
San Diego, CA
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An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated:  12/31/1969
998
mi
from 43215
Miami, FL
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated: 12/31/1969
New Age Medical Research Corp.
998
mi
from 43215
Miami, FL
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An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated:  12/31/1969
438
mi
from 43215
Lawrenceville, NJ
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated: 12/31/1969
Lawrence OB-GYN Clinical Research, LLC
438
mi
from 43215
Lawrenceville, NJ
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An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated:  12/31/1969
938
mi
from 43215
Lake Worth, FL
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated: 12/31/1969
Altus Research
938
mi
from 43215
Lake Worth, FL
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An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated:  12/31/1969
773
mi
from 43215
Leesburg, FL
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated: 12/31/1969
OB-GYN Associates of Mid-Florida, PA
773
mi
from 43215
Leesburg, FL
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An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated:  12/31/1969
417
mi
from 43215
Roswell, GA
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated: 12/31/1969
Atlanta North Gynecology, PC
417
mi
from 43215
Roswell, GA
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An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated:  12/31/1969
785
mi
from 43215
Wichita, KA
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated: 12/31/1969
Cypress Medical Research Center, LLC
785
mi
from 43215
Wichita, KA
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An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated:  12/31/1969
797
mi
from 43215
Metairie, LA
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated: 12/31/1969
Clinical Trials Management
797
mi
from 43215
Metairie, LA
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An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated:  12/31/1969
407
mi
from 43215
Saint Louis, MO
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated: 12/31/1969
Consultants in Women's Healthcare, Inc.
407
mi
from 43215
Saint Louis, MO
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An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated:  12/31/1969
369
mi
from 43215
Raleigh, NC
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated: 12/31/1969
Wake Research Associates, LLC
369
mi
from 43215
Raleigh, NC
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An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated:  12/31/1969
522
mi
from 43215
Charleston, SC
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated: 12/31/1969
Medical Research South
522
mi
from 43215
Charleston, SC
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An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated:  12/31/1969
996
mi
from 43215
Houston, TX
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated: 12/31/1969
TMC Life Research, Inc
996
mi
from 43215
Houston, TX
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An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated:  12/31/1969
1137
mi
from 43215
San Antonio, TX
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated: 12/31/1969
Clinical Trials of Texas, Inc.
1137
mi
from 43215
San Antonio, TX
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An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated:  12/31/1969
2006
mi
from 43215
Seattle, WA
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated: 12/31/1969
Seattle Women's Health, Research and Gynecology
2006
mi
from 43215
Seattle, WA
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An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated:  12/31/1969
813
mi
from 43215
Brandon, FL
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated: 12/31/1969
Gulf Coast Research Group, LLC
813
mi
from 43215
Brandon, FL
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An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated:  12/31/1969
983
mi
from 43215
South Miami, FL
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated: 12/31/1969
Visionary Investigators Network
983
mi
from 43215
South Miami, FL
Click here to add this to my saved trials
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated:  12/31/1969
767
mi
from 43215
Covington, LA
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated: 12/31/1969
Clinical Trials Management LLC
767
mi
from 43215
Covington, LA
Click here to add this to my saved trials
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated:  12/31/1969
798
mi
from 43215
New Orleans, LA
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated: 12/31/1969
Women Under Study, LLC
798
mi
from 43215
New Orleans, LA
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An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated:  12/31/1969
321
mi
from 43215
Greensboro, NC
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated: 12/31/1969
Unified Women's Clinical Research- Central Carolina
321
mi
from 43215
Greensboro, NC
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An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated:  12/31/1969
492
mi
from 43215
Birmingham, AL
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated: 12/31/1969
UAB Personal Health Clinic
492
mi
from 43215
Birmingham, AL
Click here to add this to my saved trials
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated:  12/31/1969
164
mi
from 43215
Detroit, MI
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated: 12/31/1969
Tolan Park Medical Building
164
mi
from 43215
Detroit, MI
Click here to add this to my saved trials
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated:  12/31/1969
445
mi
from 43215
Plainsboro, NJ
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated: 12/31/1969
Women's Health Research Center
445
mi
from 43215
Plainsboro, NJ
Click here to add this to my saved trials
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated:  12/31/1969
414
mi
from 43215
Philadelphia, PA
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated: 12/31/1969
Drexel University
414
mi
from 43215
Philadelphia, PA
Click here to add this to my saved trials
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated:  12/31/1969
502
mi
from 43215
Memphis, TN
An Active-Controlled, Dose-Finding Study of SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
A Phase 2, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled, Dose-Finding Study to Compare the Safety and Efficacy of Oral SCY-078 vs. Oral Fluconazole in Subjects With Acute Vulvovaginal Candidiasis
Status: Enrolling
Updated: 12/31/1969
WR-Medical Research Center of Memphis, LLC
502
mi
from 43215
Memphis, TN
Click here to add this to my saved trials
Prospective Cohort Study of HIV and Zika in Infants and Pregnancy
Prospective Cohort Study of HIV and Zika in Infants and Pregnancy
Status: Enrolling
Updated:  12/31/1969
996
mi
from 43215
Miami, FL
Prospective Cohort Study of HIV and Zika in Infants and Pregnancy
Prospective Cohort Study of HIV and Zika in Infants and Pregnancy
Status: Enrolling
Updated: 12/31/1969
University of Miami Pediatric/Prenatal HIV/AIDS
996
mi
from 43215
Miami, FL
Click here to add this to my saved trials
Prospective Cohort Study of HIV and Zika in Infants and Pregnancy
Prospective Cohort Study of HIV and Zika in Infants and Pregnancy
Status: Enrolling
Updated:  12/31/1969
4843
mi
from 43215
Belo Horizonte,
Prospective Cohort Study of HIV and Zika in Infants and Pregnancy
Prospective Cohort Study of HIV and Zika in Infants and Pregnancy
Status: Enrolling
Updated: 12/31/1969
SOM Federal University Minas Gerais Brazil NICHD CRS
4843
mi
from 43215
Belo Horizonte,
Click here to add this to my saved trials