CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 152 enrolled
Drug / intervention
Over-encapsulated 10 mg amlodipine besylate tablet +3 moredrug
Likely dose
Over-encapsulated 10 mg amlodipine besylate tabletfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02172040
NCT02172040Phase 3Completed

A Prospective Randomized Placebo Controlled Study to Evaluate the Effect of Celecoxib on the Efficacy and Safety of Amlodipine in Subjects With Hypertension Requiring Antihypertensive Therapy

Kitov Pharmaceuticals, Ltd.·interventional·Posted Jun 24, 2014·Updated Oct 10, 2018

In Brief

A Phase 3 clinical trial evaluating Over-encapsulated 10 mg amlodipine besylate tablet, Matched placebo capsule for over-encapsulated celecoxib capsule, and 2 other interventions for Hypertension. Completed, enrolled 152 participants across 10 sites.

Detailed Summary

The purpose of this study was to evaluate the effect of celecoxib on the efficacy and safety of amlodipine besylate in subjects with newly diagnosed hypertension requiring antihypertensive therapy. This study was conducted to support a future marketing application for KIT-302. Kitov Pharma Ltd. (Kitov) is developing KIT-302, an oral fixed combination drug product (FCDP) consisting of the calcium channel blocker amlodipine besylate and the nonsteroidal anti-inflammatory drug (NSAID) celecoxib, as a "convenience reformulation" FCDP to facilitate and improve patient compliance with the once a day (qd) administration of its individual components, amlodipine and celecoxib. The formulation of KIT-302 consists of amlodipine besylate and celecoxib co-formulated in a single immediate release tablet. However, for this study, two separate capsules were utilized: one containing a commercial celecoxib capsule (Celebrex®) or matched placebo capsule and one containing a commercial amlodipine besylate tablet (Norvasc®) or matched placebo tablet. The study hypothesis was that treatment with the amlodipine besylate containing capsule plus the celecoxib containing capsule would reduce blood pressure (BP) in subjects with hypertension with an efficacy that is not substantially inferior to the effect of amlodipine besylate alone (i.e., the amlodipine containing capsule plus the matched placebo for the celecoxib capsule). The United States (US) Food and Drug Administration (FDA) recently approved KIT-302, under the brand name Consensi® (amlodipine and celecoxib) tablets \[New Drug Application (NDA) 210045\] for the following indication: "patients for whom treatment with amlodipine for hypertension and celecoxib for osteoarthritis are appropriate. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions."

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHypertension
CountriesUnited Kingdom
Collaborators--

Timeline

Phase 3CompletedFinished
201520162017201820192020202120222023202420252026
First PostedJun 24, 2014
Enrollment StartJun 26, 2014
Primary CompletionNov 19, 2015
TodayJul 2, 2026
Enrollment to primary: 1.4 yearsPosted 12.0 years ago

Interventions

Over-encapsulated 10 mg amlodipine besylate tabletdrug

Over-encapsulated 10 mg amlodipine besylate tablet once a day for two weeks

Matched placebo capsule for over-encapsulated celecoxib capsuledrug

Matched placebo capsule for over-encapsulated celecoxib capsule once a day for two weeks

Over-encapsulated 200 mg celecoxib capsuledrug

Over-encapsulated 200 mg celecoxib capsule once a day for two weeks

Matched placebo capsule for over-encapsulated amlodipine besylate tabletdrug

Matched placebo capsule for over-encapsulated amlodipine besylate tablet once a day for two weeks