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NCT03442621
Relacorilant Food Effect Study in Healthy Subjects
Phase 1 trial testing Relacorilant Fasted in Healthy in 30 participants. Completed in 9 March 2018.
28 February 2018
Quick facts
| Lead sponsor | Corcept Therapeutics |
|---|---|
| Phase | Phase 1 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | crossover |
| Masking | none |
| Primary purpose | other |
| Enrollment | 30 |
| Start date | 16 January 2018 |
| Primary completion | 28 February 2018 |
| Estimated completion | 9 March 2018 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Relacorilant Fasted — full drug profile →
- Relacorilant with a high fat breakfast — full drug profile →
- Relacorilant with a moderate breakfast — full drug profile →
Conditions studied
- Healthy — all drugs for Healthy →
- Food-drug Interaction — all drugs for Food-drug Interaction →
Sponsor
Corcept Therapeutics — full company profile →
Who can join
Adults 18 to 65, any sex, with Healthy or Food-drug Interaction. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This is an open-label, randomized, single-dose, 3-period crossover, Williams' design, food-interaction (fasted and fed arms) study conducted in healthy subjects.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Overcoming Taxane Resistance: Preclinical and Phase 1 Studies of Relacorilant, a Selective Glucocorticoid Receptor Modulator, with Nab-Paclitaxel in Solid Tumors.
Munster PN, Greenstein AE, Fleming GF, Borazanci E, et al · · 2022 · cited 25× · PMID 35583817 · DOI 10.1158/1078-0432.ccr-21-4363
Verify or expand the search:
- PubMed search for NCT03442621
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Corcept Therapeutics trials
Trials by the same sponsor.
- NCT07240116 — Study Evaluating the Bioavailability of Miricorilant With Optional Food Effect Assessment in Healthy Adult Subjects · Phase 1 · completed
- NCT06829537 — Study of the Prevalence of Endogenous Hypercortisolism in Patients With Resistant Hypertension (MOMENTUM) · completed
- NCT06928779 — Effects of Hepatic Impairment on the Pharmacokinetics of Dazucorilant · Phase 1 · completed
- NCT06495944 — Impact of Itraconazole on the Pharmacokinetics and Safety of Dazucorilant in Healthy, Adult Participants · Phase 1 · completed
- NCT05772169 — Study to Determine the Prevalence of Hypercortisolism in Patients With Type 2 Diabetes and Treatment With Korlym® (Mifep · Phase 4 · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03442621 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Corcept Therapeutics
- Last refreshed: 17 May 2018
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03442621.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing