TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

CAVERJECT IMPULSE

ALPROSTADIL Prostaglandin Receptor Agonists
Approved 2002-06-11
1
Indication
--
Phase 3 Trials
23
Years on Market

Details

Status
Prescription
First Approved
2002-06-11
Routes
INJECTION
Dosage Forms
INJECTABLE

Companies

Active Ingredient: ALPROSTADIL

CAVERJECT IMPULSE Approval History

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What CAVERJECT IMPULSE Treats

1 indications

CAVERJECT IMPULSE is approved for 1 conditions since its original approval in 2002. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Erectile Dysfunction
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.

CAVERJECT IMPULSE FDA Label Details

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Indications & Usage

FDA Label (PDF)

CAVERJECT IMPULSE is a prostaglandin E1 agonist indicated • For the treatment of erectile dysfunction • As an adjunct to other diagnostic tests in the diagnosis of erectile dysfunction . 1.1 Erectile Dysfunction CAVERJECT IMPULSE is indicated for the treatment of erectile dysfunction. 1.2 Diagnostic Test CAVERJECT IMPULSE is indicated as an adjunct to other diagnostic tests in the diagnosis of erectile dysfunction.

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Data Sources

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