CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 74 enrolled
Drug / intervention
Estradiol +3 moredrug
Likely dose
Estradiol 0.1 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03689543
NCT03689543Phase 2Completed

The Effects of an ER Beta Agonist (Lilly Compound LY500307) on Estradiol-withdrawal-induced Mood Symptoms in Women With Past Perimenopausal Depression

National Institute of Mental Health (NIMH)·interventional·Posted Sep 28, 2018·Updated Sep 16, 2025

In Brief

A Phase 2 clinical trial evaluating Estradiol, ER Beta Agonist, and 2 other interventions for Perimenopause-Related Depression. Completed, enrolled 74 participants across 1 site.

Detailed Summary

Background: Our previous studies have found that women who had depression during the perimenopause may have mood symptoms again if they stop estrogen therapy. Estrogen acts in the brain and other tissues by binding to estrogen receptors. There are two main types of estrogen receptors. They are estrogen receptor alpha and beta. Several studies have shown that estrogen receptor beta may play an important role in anxiety- and depressive-like behaviors in animals. Objectives: To examine a possible mechanism mediating the effects of estradiol-withdrawal on mood symptoms in asymptomatic postmenopausal women with a past perimenopausal depression. To evaluate the efficacy and safety of a selective estrogen receptor (ER) beta agonist (Lilly Compound LY500307) to prevent estradiol withdrawal-induced mood symptoms. Eligibility: Healthy, non-depressed postmenopausal women, ages 45 to 65, with a well-documented past perimenopause-related depression (within 12 years) and whose mood systems got better with estradiol Design: Participants will be screened with: Medical history Physical exam Blood tests Psychiatric interview Gynecological exam * Participants able to get pregnant must use effective barrier birth control throughout the study. * During the first 3 weeks, participants will wear an estrogen patch. It is 1x2 inches and will be replaced every 3 days. * For the next 3 weeks, participants will take 3 study capsules every morning. They will not know if they get the study drug or placebo. * Some participants will also take a progesterone-like drug for 1 week at the end of the medication phase of the study. * Participants will have 9 one-hour study visits. They will have blood samples and vital signs taken. They will answer questions about mood and behavior symptoms. * Participants will keep a daily log of these symptoms. * Participants will have 2 transvaginal ultrasounds. A probe is temporarily placed 2-3 inches into the vaginal canal and sound waves are used to create pictures of the lining of the uterus. * Participants will have a final visit 4 weeks after stopping the study drug. They will answer questions about mood and side effects.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
20192020202120222023202420252026
First PostedSep 28, 2018
Enrollment StartMay 23, 2019
Primary CompletionSep 9, 2024
TodayJul 2, 2026
Enrollment to primary: 5.3 yearsPosted 7.8 years ago

Interventions

Estradioldrug

Estradiol patch 0.1 mg transdermal every three days for three weeks

ER Beta Agonistdrug

Lilly Compound LY500307, a selective estrogen receptor (ER) beta agonist

Placeboother

Placebo orally once daily

Proveradrug

Provera 5 mg orally once a day for one week after completion of randomization