TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

RAPIBLYK

LANDIOLOL HYDROCHLORIDE
Cardiovascular Approved 2024-11-22
2
Indications
--
Phase 3 Trials
1
Years on Market

Details

Status
Prescription
First Approved
2024-11-22
Routes
INTRAVENOUS
Dosage Forms
POWDER

Companies

Active Ingredient: LANDIOLOL HYDROCHLORIDE

RAPIBLYK Approval History

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What RAPIBLYK Treats

3 indications

RAPIBLYK is approved for 3 conditions since its original approval in 2024. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Supraventricular Tachycardia
  • Atrial Fibrillation
  • Atrial Flutter
Source: FDA Label

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Active Pipeline

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Ongoing clinical trials by development phase

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

RAPIBLYK FDA Label Details

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Indications & Usage

FDA Label (PDF)

RAPIBLYK is indicated for the short-term reduction of ventricular rate in adults with supraventricular tachycardia including atrial fibrillation and atrial flutter. RAPIBLYK is a beta adrenergic blocker indicated for the short-term reduction of ventricular rate in adults with supraventricular tachycardia including atrial fibrillation and atrial flutter.

RAPIBLYK Patents & Exclusivity

Latest Patent: Apr 2034
Exclusivity: Nov 2029

Patents (1 active)

US10722516 Expires Apr 25, 2034

Exclusivity

NCE Until Nov 2029
Source: FDA Orange Book

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.