Study Evaluating the Efficacy and Safety of Three Formulations of Ultra-low Dose Estriol Vaginal Gel (0.005%, 0.002%, 0.0008% Estriol Vaginal Gel) for the Treatment of Vaginal Dryness in Postmenopausal Women With Vulvovaginal Atrophy

PHASE2CompletedINTERVENTIONAL
Enrollment

283

Participants

Timeline

Start Date

October 31, 2016

Primary Completion Date

May 31, 2018

Study Completion Date

May 31, 2018

Conditions
Vaginal Atrophy
Interventions
DRUG

Estriol

DRUG

Placebo

Trial Locations (23)

2800

For additional information regarding investigative sites for this trial, contact ITF Research Pharma S.L.U., Tatabánya

6725

For additional information regarding investigative sites for this trial, contact ITF Research Pharma S.L.U, Szeged

For additional information regarding investigative sites for this trial, contact ITF Research Pharma S.L.U., Szentes

8000

For additional information regarding investigative sites for this trial, contact ITF Research Pharma S.L.U, Székesfehérvár

27100

For additional information regarding investigative sites for this trial, contact ITF Research Pharma S.L.U., Pavia

30120

For additional information regarding investigative sites for this trial, contact ITF Research Pharma S.L.U., Murcia

39008

For additional information regarding investigative sites for this trial, contact ITF Research Pharma S.L.U., Santander

41124

For additional information regarding investigative sites for this trial, contact ITF Research Pharma S.L.U., Modena

46010

For additional information regarding investigative sites for this trial, contact ITF Research Pharma S.L.U., Valencia

53100

For additional information regarding investigative sites for this trial, contact ITF Research Pharma S.L.U., Siena

80022

For additional information regarding investigative sites for this trial, contact ITF Research Pharma S.L.U., Barcelona

88100

For additional information regarding investigative sites for this trial, contact ITF Research Pharma S.L.U., Catanzaro

95123

For additional information regarding investigative sites for this trial, contact ITF Research Pharma S.L.U., Catania

602 00

For additional information regarding investigative sites for this trial, contact ITF Research Pharma S.L.U, Brno

370 01

For additional information regarding investigative sites for this trial, contact ITF Research Pharma S.L.U., České Budějovice

779 00

For additional information regarding investigative sites for this trial, contact ITF Research Pharma S.L.U., Olomouc

Unknown

For additional information regarding investigative sites for this trial, contact ITF Research Pharma S.L.U., Olomouc

For additional information regarding investigative sites for this trial, contact ITF Research Pharma S.L.U., Prague

For additional information regarding investigative sites for this trial, contact ITF Research Pharma S.L.U., Vsetín

397 01

For additional information regarding investigative sites for this trial, contact ITF Research Pharma S.L.U., Písek

141 86

For additional information regarding investigative sites for this trial, contact ITF Research Pharma S.L.U., Huddinge

434 30

For additional information regarding investigative sites for this trial, contact ITF Research Pharma S.L.U., Kungsbacka

171 76

For additional information regarding investigative sites for this trial, contact ITF Research Pharma S.L.U., Stockholm

All Listed Sponsors
lead

ITF Research Pharma, S.L.U.

INDUSTRY

NCT02967510 - Study Evaluating the Efficacy and Safety of Three Formulations of Ultra-low Dose Estriol Vaginal Gel (0.005%, 0.002%, 0.0008% Estriol Vaginal Gel) for the Treatment of Vaginal Dryness in Postmenopausal Women With Vulvovaginal Atrophy | Biotech Hunter | Biotech Hunter