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NCT06906341 · ClinicalTrials.gov registry record · Phase 2

Relacorilant in Combination With Different Treatment Regimens in Patients With Gynecological Cancers

A Phase 2 study of Ovarian Cancer and Endometrial Cancer, sponsored by Corcept Therapeutics.

Recruiting
Registry status
Phase 2
Development phase
270
Enrollment target
20
Study locations

NCT06906341 is a Phase 2 study of Ovarian Cancer and Endometrial Cancer that is actively recruiting participants, run by Corcept Therapeutics. The registered enrollment target is 270 participants, below the 728-participant average among 322 other Ovarian Cancer trials with a reported enrollment target (63% lower). The trial reports 20 study locations across 11 states.

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The verdict

NCT06906341, a Phase 2 study of Ovarian Cancer and Endometrial Cancer, is actively recruiting participants, sponsored by Corcept Therapeutics.

RECRUITING
Registry status
Phase 2
Development phase
270 participants
Enrollment target
20
Study locations

Study Summary

This is a Phase 2, open-label, global, multi-arm study to evaluate efficacy and safety of relacorilant in combination with other treatments in patients with gynecological cancers.

Interventions

  • DRUG Relacorilant 150 mg once daily (QD)
  • DRUG Nab-paclitaxel 80 mg/m^2
  • DRUG Bevacizumab 10 mg/kg

Study Locations (20)

Other

  • 328 - Aalst
  • 326 - Charleroi
  • 325 - Hasselt
  • 108 - Leuven
  • 306 - Lille
  • 307 - Nancy

California

  • 150 - Palo Alto
  • 014 - San Francisco

Florida

  • 544 - Fort Myers
  • 543 - West Palm Beach

Missouri

  • 334 - Kansas City
  • 521 - St Louis

Virginia

  • 522 - Fairfax
  • 300 - Norfolk

Minnesota

  • 518 - Minneapolis

New Mexico

  • 292 - Albuquerque

Ohio

  • 304 - Centerville

Trial Details

FieldValue
Enrollment Target 270 participants
Start Date 2025-04-11
Est. Completion 2026-12
Phase Phase 2

Sponsor

Corcept Therapeutics

54 total trials

What the Registry Record Tells You About NCT06906341

The ClinicalTrials.gov registry entry for NCT06906341 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 270 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 728-participant average among 322 other Ovarian Cancer trials with a reported enrollment target (63% lower). The listed sponsor is Corcept Therapeutics, which has 54 total studies on file at ClinicalTrials.gov.

The record links to 4 conditions, with Ovarian Cancer appearing as the primary indexed condition, and to 3 interventions - of which Relacorilant 150 mg once daily (QD) is the first listed.

NCT06906341 reports 20 study locations spanning 11 distinct geographic areas - top geographies include Other, California, Florida.

Frequently Asked Questions

What is clinical trial NCT06906341 about?

NCT06906341 is a clinical study titled "Relacorilant in Combination With Different Treatment Regimens in Patients With Gynecological Cancers". This is a Phase 2, open-label, global, multi-arm study to evaluate efficacy and safety of relacorilant in combination with other treatments in patients with gynecological cancers.

What is the current status of trial NCT06906341?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 270 participants. The study started on 2025-04-11. Estimated completion is 2026-12.

What conditions does trial NCT06906341 study?

This clinical trial studies the following conditions: Ovarian Cancer, Endometrial Cancer, Fallopian Tube Cancer, Peritoneal Neoplasms.

What interventions are being tested in trial NCT06906341?

The interventions under investigation include: Relacorilant 150 mg once daily (QD) (DRUG), Nab-paclitaxel 80 mg/m^2 (DRUG), Bevacizumab 10 mg/kg (DRUG).

Who is sponsoring clinical trial NCT06906341?

This trial is sponsored by Corcept Therapeutics, which has 54 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06906341 being conducted?

This trial has 20 study locations across California, Florida, Minnesota, Missouri, New Mexico. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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