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NCT06048887
Single and Multiple-Ascending Dose Study of CRN04894 in Healthy Volunteers
Phase 1 trial testing CRN04894 Oral Solution in Healthy Volunteers in 88 participants. Completed in 11 April 2022.
11 April 2022
Quick facts
| Lead sponsor | Crinetics Pharmaceuticals Inc. |
|---|---|
| Phase | Phase 1 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | double |
| Primary purpose | treatment |
| Enrollment | 88 |
| Start date | 18 December 2020 |
| Primary completion | 11 April 2022 |
| Estimated completion | 11 April 2022 |
| Sites | 1 location across United States |
Drugs / interventions tested
- CRN04894 Oral Solution — full drug profile →
- Placebo Oral Solution
Conditions studied
- Healthy Volunteers — all drugs for Healthy Volunteers →
Sponsor
Crinetics Pharmaceuticals Inc. — full company profile →
Who can join
Adults 18 to 55, any sex, with Healthy Volunteers. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
A Phase 1, first-in-human, double-blind, randomized, placebo-controlled study to evaluate the safety of CRN04894 in healthy volunteers as well as the relationship between exposure and pharmacodynamic (PD) parameters.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Future Directions in the Management of Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.
Sarafoglou K, Auchus RJ. · · 2025 · cited 11× · PMID 39836617 · DOI 10.1210/clinem/dgae759
Verify or expand the search:
- PubMed search for NCT06048887
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
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Other Crinetics Pharmaceuticals Inc. trials
Trials by the same sponsor.
- NCT07221084 — A Study to Assess Pharmacokinetics, Safety, and Tolerability of Atumelnant in Healthy Japanese and Caucasian Participant · Phase 1 · completed
- NCT05907291 — Evaluate the Safety, Efficacy, and Pharmacokinetics of CRN04894 in Participants With Congenital Adrenal Hyperplasia (Tou · Phase 2 · completed
- NCT05361668 — Study to Evaluate the Safety, PK, and Dose Response of Paltusotine in Subjects With Carcinoid Syndrome · Phase 2 · completed
- NCT04246749 — Mass Balance and Pharmacokinetics of [14C]-CRN00808 in Healthy Volunteers · Phase 1 · completed
- NCT03936166 — A Single and Multiple-Ascending Dose Study of CRN01941 in Healthy Adult Volunteers · Phase 1 · 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 NCT06048887 (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 Crinetics Pharmaceuticals Inc.
- Last refreshed: 21 September 2023
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/NCT06048887.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing