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NCT03847506: REVERT-K
Evaluate Efficacy and Safety of Ezetimibe/Rosuvastatin and Candesartan Cilexetil/Amlodipine Besylate Combination Tablets
Phase 4 trial testing Ezetimibe/Rosuvastatin in Hypertension, Hyperlipidemia in 127 participants. Completed in 2 December 2020.
2 December 2020
Quick facts
| Lead sponsor | HK inno.N Corporation |
|---|---|
| Phase | Phase 4 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | quadruple |
| Primary purpose | treatment |
| Enrollment | 127 |
| Start date | 5 July 2018 |
| Primary completion | 2 December 2020 |
| Estimated completion | 2 December 2020 |
| Sites | 1 location across South Korea |
Drugs / interventions tested
- Ezetimibe/Rosuvastatin — full drug profile →
- Candesartan cilexetil/Amlodipine besylate — full drug profile →
- Candesartan cilexetil (CILEXETIL) — full drug profile →
Conditions studied
- Hypertension, Hyperlipidemia — all drugs for Hypertension, Hyperlipidemia →
Sponsor
HK inno.N Corporation — full company profile →
Who can join
Adults 19 to 74, any sex, with Hypertension, Hyperlipidemia. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
To evaluate the efficacy and the safety of concomitant use of Ezetimibe/Rosuvastatin combination tablets and Candesartan cilexetil/Amlodipine besylate combination tablets compared to each combination tablet alone in patients with essential hypertension (HTN) and hyperlipidemia.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT03847506
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of Ezetimibe/Rosuvastatin
Trials testing the same drug.
- NCT05889143 — A Study to Evaluate the Efficacy and Safety of CREZET Tablet · active not recruiting
- NCT04158076 — Evaluating the Efficacy and Safety of Co-administrated Rosuvastatin/Ezetimibe and Telmisartan/Amlodipine · Phase 3 · completed
- NCT03872232 — Evaluating the Efficacy and Safety of Co-administrated Rosuvastatin/Ezetimibe and Telmisartan · Phase 3 · completed
- NCT03532854 — Evaluating a Pharmacokinetic Drug Interaction Between LGEV1801 and LGEV1802 · Phase 1 · completed
Other HK inno.N Corporation trials
Trials by the same sponsor.
- NCT07277712 — A Study to Evaluate the Pharmacokinetics and Food-effect of IN-M00002 Tablet in Healthy Adult Volunteers · Phase 1 · not yet recruiting
- NCT07192263 — Study to Evaluate the Efficacy and Safety of IN-B00009 Injection in Adults With Obesity or Overweight Without Diabetes M · Phase 3 · not yet recruiting
- NCT06736912 — This Study Aims to Evaluate the Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Properties and Food Effect of · Phase 1 · not yet recruiting
- NCT06725355 — To Compare the Pharmacokinetics and Safety After a Single Dose Administration of IN-G00002 and IN-R00002 in Healthy Adul · Phase 1 · active not recruiting
- NCT06332638 — PK, PD and Safety of Tegoprazan 12.5 mg After Oral Administration in Healthy Subjects · Phase 1 · unknown
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 NCT03847506 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by HK inno.N Corporation
- Last refreshed: 10 May 2022
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/NCT03847506.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing