Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 2 Interventional Results available

Study of Relacorilant in Combination With Nab-Paclitaxel for Patients With Recurrent Platinum-Resistant Ovarian, Fallopian Tube, or Primary Peritoneal Cancer

ClinicalTrials.gov ID: NCT03776812

Public ClinicalTrials.gov record NCT03776812. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 25, 2026, 1:48 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Randomized, Open-Label, 3-arm Study of Relacorilant in Combination With Nab-Paclitaxel for Patients With Recurrent Platinum-Resistant Ovarian, Fallopian Tube, or Primary Peritoneal Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a Phase 2, open-label, randomized, 3-arm study to evaluate progression-free survival (PFS) in patients with recurrent platinum-resistant ovarian, fallopian tube, or primary peritoneal cancer treated with intermittent or continuous regimens of relacorilant in combination with nab-paclitaxel compared with patients treated with nab-paclitaxel alone.

Study identification

NCT ID
NCT03776812
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Corcept Therapeutics
Industry
Enrollment
178 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 5, 2019 (Actual)
Primary completion
Mar 16, 2021 (Actual)
Completion
Jul 12, 2023 (Actual)
Last update posted
Oct 7, 2025

2019 – 2023

United States locations

U.S. sites
12
U.S. states
9
U.S. cities
9
Facility City State ZIP Site status
Site Reference ID/Investigator #004 Birmingham Alabama 35249 —
Site Reference ID/Investigator #038 Scottsdale Arizona 85258 —
Site Reference ID/Investigator #032 Denver Colorado 80045 —
Site Reference ID/Investigator #001 Chicago Illinois 60637 —
Site Reference ID/Investigator #106 Boston Massachusetts 02215 —
Site Reference ID/Investigator #128 Boston Massachusetts 02215 —
Site Reference ID/Investigator #051 New York New York 10065 —
Site Reference ID/Investigator #169 New York New York 10065 —
Site Reference ID/Investigator #170 New York New York 10065 —
Site Reference ID/Investigator #127 Pittsburgh Pennsylvania 15213 —
Site Reference ID/Investigator #135 Charlottesville Virginia 22908 —
Site Reference ID/Investigator #121 Milwaukee Wisconsin 53226 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 12 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03776812, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 7, 2025 · Synced Oct 25, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03776812 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →