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NCT04703868
A Study to Compare the Safety, Pharmacokinetics and Pharmacodynamics of YPI 011 to Rabeprazole in Healthy Adult Subjects
Phase 1 trial testing Rabeprazole Sodium 10mg in Gastroesophageal Reflux Disease in 88 participants. Completed in 14 June 2021.
1 June 2021
Quick facts
| Lead sponsor | Yungjin Pharm. Co., Ltd. |
|---|---|
| Phase | Phase 1 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | crossover |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 88 |
| Start date | 13 January 2021 |
| Primary completion | 1 June 2021 |
| Estimated completion | 14 June 2021 |
| Sites | 1 location across South Korea |
Drugs / interventions tested
- Rabeprazole Sodium 10mg
- Rabeprazole Sodium 20mg — full drug profile →
Conditions studied
- Gastroesophageal Reflux Disease — all drugs for Gastroesophageal Reflux Disease →
Sponsor
Yungjin Pharm. Co., Ltd. — full company profile →
Who can join
Adults 19 to 55, any sex, with Gastroesophageal Reflux Disease. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
A study to compare the safety, pharmacokinetics and pharmacodynamics of YPI 011 to Rabeprazole in healthy adult subjects
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Development of a Fast Onset Proton Pump Inhibitor: Comparison of Fixed-Dose Combination of Rabeprazole and Sodium Bicarbonate (YPI-011) to the Conventional Enteric-Coated Rabeprazole.
Bae S, Kwon J, Lee MH, Yu KS, et al · · 2023 · cited 1× · PMID 36814893 · DOI 10.2147/dddt.s391716
Verify or expand the search:
- PubMed search for NCT04703868
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Yungjin Pharm. Co., Ltd. trials
Trials by the same sponsor.
- NCT03261427 — Evaluate the Pharmacokinetic Characteristics and Safety/Tolerability of YNP-1807 Compared to Lyrica® After Oral Administ · Phase 1 · completed
- NCT03056209 — Safety, Tolerability and Pharmacokinetic Study of KL1333 in Healthy Male Volunteers · Phase 1 · completed
- NCT03275025 — A Phase 2 Study to Evaluate the Safety and Efficacy of YRA-1909 in Patients With Rheumatoid Arthritis · Phase 2 · completed
- NCT02272634 — A Phase 2a Study to Assess Safety, Daily Symptoms, PK, and Biomarkers of YPL-001 in COPD Patients · Phase 2 · 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 NCT04703868 (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 Yungjin Pharm. Co., Ltd.
- Last refreshed: 24 January 2024
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/NCT04703868.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing