CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 1,116 enrolled
Drug / intervention
Etripamil NSdrug
Likely dose
Etripamil NS 70 mgfrom 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/NCT04072835
NCT04072835Phase 3Completed

The NODE-303 Study: Multi-Centre, Multi-National,Open Label, Safety Study of Etripamil Nasal Spray for Patients With Paroxysmal Supraventricular Tachycardia.

Milestone Pharmaceuticals Inc.·interventional·Posted Aug 28, 2019·Updated May 23, 2024

In Brief

A Phase 3 clinical trial evaluating Etripamil NS for Paroxysmal Supraventricular Tachycardia. Completed, enrolled 1,116 participants across 124 sites in 5 countries.

Detailed Summary

NODE-303 was a multi-center, open label study to evaluate the safety of etripamil NS in participants with Paroxysmal Supraventricular Tachycardia (PSVT). Participants were provided with an ambulatory Cardiac Monitoring System (CMS) to help document PSVT episodes. The CMS was self-applied by the participant, when they felt the onset of PSVT symptoms. Participants self-administered etripamil NS if vagal maneuver was ineffective. After an episode of PSVT where study drug was administered, the participant returned to the investigative site and had the option to continue in NODE-303 and manage up to three subsequent episodes of PSVT with etripamil NS for a maximum of four episodes.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesArgentina, Brazil, Canada, Colombia, United States
CollaboratorsIQVIA Biotech

Timeline

Phase 3CompletedFinished
2020202120222023202420252026
First PostedAug 28, 2019
Enrollment StartSep 23, 2019
Primary CompletionJan 26, 2023
TodayJul 2, 2026
Enrollment to primary: 3.3 yearsPosted 6.8 years ago

Interventions

Etripamil NSdrug

Participants were provided with an ambulatory Cardiac Monitoring System (CMS) to help document PSVT episodes. The CMS was self-applied by the participant, when PSVT symptoms begin. Participants self-administered etripamil NS if vagal maneuver was ineffective. After implementation of protocol amendment 2.1, participants had the option to administer a second dose of etripamil 70 mg 10 minutes after the first dose, if symptoms persisted. After an episode of PSVT where drug was administered, the participant returned to the investigative site for a study visit and was given the option to continue in NODE-303 and manage up to three subsequent episodes of PSVT with etripamil NS for a maximum of four episodes.