Ireland
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Priya Life Science Compound trial record
Compound · clinical trials

Relacorilant clinical trials

Also listed in trial records as Lifyorli, CORT125134
Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 5 trials in our USA, France, Spain, Italy, Poland, Belgium, Canada, South Korea, Israel, Germany, UK, Brazil, Australia, Netherlands and Austria registers that name Relacorilant as an intervention. Synced 10 Nov 2026
5Current trials
2Recruiting now
2Lead sponsors
15Country registers
At a glance

Relacorilant is named as an intervention in 5 current clinical trials in our USA, France, Spain, Italy, Poland, Belgium, Canada, South Korea, Israel, Germany, UK, Brazil, Australia, Netherlands and Austria registers. 2 are recruiting patients now. The most common phase is Phase 2. The sponsor with the most trials is Corcept Therapeutics (4). The most-studied condition is Peritoneal Neoplasms.

Where Relacorilant is approved

All regulators →

Of the three regulators tracked here, the first to approve Relacorilant was the US, on 25 Mar 2026.

USUnited States (FDA)
25 Mar 2026
Lifyorli (copackaged)
NDA220641 on Drugs@FDA
First original NDA/BLA approval
EUEuropean Union (EMA)
No centralised EU authorisation (it may be authorised nationally)
First centralised authorisation
CACanada (Health Canada)
No new-drug Notice of Compliance since 1994
First new-drug NOC

From the regulators' own registers: FDA Drugs@FDA, the EMA medicines list and Health Canada's Notice of Compliance database. Dates are the first listed approval of a product containing only this substance; combination products and nationally authorised EU medicines are not counted.

Relacorilant patents and exclusivity

Expiry tracker →

Protections still running for marketed products containing Relacorilant, as listed by the regulators. Expired patents and exclusivities, and discontinued products, are not shown.

US FDA Orange Book Lifyorli (copackaged)
  • 10 listed patents; the last listed expires 22 Dec 2041 (US 12152028).
  • Latest patent on the drug substance itself: 24 May 2033 (US 11576907).
  • Exclusivity NCE: New chemical entity, until 25 Mar 2031.
See the Orange Book listing for NDA 220641

Reproduced from the FDA Orange Book and Purple Book (checked 8 Nov 2026) and the European Commission's Union Register of medicinal products (CC BY 4.0; the EU expiry date is calculated exactly as the Commission's register displays it). Listed patents and dates are as submitted to or published by the regulator and may not reflect litigation, invalidation, settlements, lapsed fees or later extensions. This is not legal advice or a freedom-to-operate opinion, and it does not say when a generic or biosimilar will launch.

How Relacorilant works

All drug targets →
  • Glucocorticoid receptor antagonist Antagonist
    Target: NR3C1 nuclear receptor subfamily 3 group C member 1
    ✓ In ChEMBL and the Guide to Pharmacology
Diseases it has been tested for in clinical trials, by furthest phase
  • Cushing syndromePhase 3
  • Impaired glucose tolerancePhase 3
  • Adrenal gland hyperfunctionPhase 3
  • Congenital adrenal hyperplasiaPhase 3
  • Fallopian tube cancerPhase 3
  • Hypertensive disorderPhase 3
  • Malignant epithelial tumor of ovaryPhase 3
  • Ovarian carcinomaPhase 3
  • Pancreatic ductal adenocarcinomaPhase 3
  • Primary peritoneal carcinomaPhase 3
18 diseases in all

Mechanisms and diseases from ChEMBL via the Open Targets Platform (release 26.09), ChEMBL record CHEMBL4068611, CC BY-SA 3.0. Targets checked against the IUPHAR/BPS Guide to PHARMACOLOGY (2026.3.1), ligand 13830, CC BY-SA 4.0. Trial phases are not approvals: approved uses are shown from the regulators' own records where we hold them.

Patient leaflets for Relacorilant

The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.

  • UK
    United Kingdom: Search MHRA Products
    Patient information leaflets and SmPCs for UK-licensed products.
  • US
    United States: Search DailyMed
    FDA-approved labels, including patient and medication guides.

Leaflets differ between brands and countries; always read the one that comes with your own medicine. This is regulatory information, not medical advice.

Trials by status

  • Recruiting240%
  • Not yet open120%
  • Active, closed240%

Trials by phase

  • Phase 2480%
  • Phase 3120%
01

Clinical trials of Relacorilant

5 trials
StudyPhaseStatusLead sponsorRegisters
Relacorilant in Combination With Different Treatment Regimens in Patients With Gynecological Cancers
NCT06906341 · Ovarian Cancer, Fallopian Tube Cancer, Peritoneal Neoplasms
Phase 2 Recruiting Corcept Therapeutics USA, Germany, France, Spain, Italy, Belgium, Poland, South Korea
Relacorilant With Nab-Paclitaxel and Gemcitabine in Patients With Metastatic Pancreatic Adenocarcinoma
NCT07259317 · ClinicalTrials.gov ↗ · Adenocarcinoma, Carcinoma, Pancreatic Ductal
Phase 2 Recruiting Corcept Therapeutics USA
Relacorilant and Nab-Paclitaxel in Recurrent or Metastatic Cervical Cancer
NCT07763496 · ClinicalTrials.gov ↗ · Recurrent or Metastatic Cervical Cancer
Phase 2 Not yet open ARCAGY/ GINECO GROUP France
Relacorilant in Combination With Nab-Paclitaxel in Advanced, Platinum-Resistant, High-Grade Epithelial Ovarian, Primary Peritoneal, or Fallopian-Tube Cancer
NCT05257408 · Ovarian Neoplasm, Fallopian Tube Neoplasms, Peritoneal Neoplasms
Phase 3 Active, closed Corcept Therapeutics UK, USA, France, Spain, Italy, Belgium, Poland, Canada, Brazil, South Korea, Australia, Israel
Extension Study to Evaluate the Safety of Long-Term Use of Relacorilant in Patients With Cushing Syndrome
NCT03604198 · Cushing Syndrome
Phase 2 Active, closed Corcept Therapeutics USA, Germany, Spain, Italy, Netherlands, Poland, Austria, Canada, Israel

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.

02

Conditions studied with Relacorilant

10 conditions
Peritoneal Neoplasms2Ovarian Neoplasm1Fallopian Tube Neoplasms1Adenocarcinoma1Carcinoma, Pancreatic Ductal1Ovarian Cancer1Fallopian Tube Cancer1Endometrial Cancer1Cushing Syndrome1Recurrent or Metastatic Cervical Cancer1
05

Related compounds

06

Questions about Relacorilant trials

How many clinical trials are testing Relacorilant?

5 current trials in our USA, France, Spain, Italy, Poland, Belgium, Canada, South Korea, Israel, Germany, UK, Brazil, Australia, Netherlands and Austria registers name Relacorilant (also registered as CORT125134) as a drug or biological intervention, as of the registry sync on 10 November 2026. Completed and withdrawn studies are not counted.

Are Relacorilant trials recruiting patients?

Yes. 2 of the 5 trials are recruiting: 2 with sites in USA, 1 with sites in France, 1 with sites in Spain, 1 with sites in Italy, 1 with sites in Poland, 1 with sites in Belgium, 1 with sites in South Korea and 1 with sites in Germany. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors Relacorilant clinical trials?

Corcept Therapeutics (4) and ARCAGY/ GINECO GROUP (1). The number in brackets is how many trials each organisation leads.

Where does this information come from?

Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how Relacorilant works or whether it is effective, and it is not medical advice.

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How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records — it is not written from memory, and nothing here describes how Relacorilant works or whether it is effective. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists Relacorilant (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 10 Nov 2026. How every register is built: methodology · fixes we have made: corrections log.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.