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NCT03847506: REVERT-K

Evaluate Efficacy and Safety of Ezetimibe/Rosuvastatin and Candesartan Cilexetil/Amlodipine Besylate Combination Tablets

Completed Phase 4 Last updated 10 May 2022
What this trial tests

Phase 4 trial testing Ezetimibe/Rosuvastatin in Hypertension, Hyperlipidemia in 127 participants. Completed in 2 December 2020.

Timeline
5 July 2018
Primary endpoint
2 December 2020
2 December 2020

Quick facts

Lead sponsorHK inno.N Corporation
PhasePhase 4
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment127
Start date5 July 2018
Primary completion2 December 2020
Estimated completion2 December 2020
Sites1 location across South Korea

Drugs / interventions tested

Conditions studied

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.

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Other trials of Ezetimibe/Rosuvastatin

Trials testing the same drug.

Other HK inno.N Corporation trials

Trials by the same sponsor.

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Data sources for this page

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