TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

CYTOVENE

GANCICLOVIR SODIUM
Approved 1989-06-23
7
Indications
--
Phase 3 Trials
3
Priority Reviews
36
Years on Market

Details

Status
Discontinued
First Approved
1989-06-23
Routes
INJECTION, ORAL
Dosage Forms
INJECTABLE, CAPSULE

Companies

Active Ingredient: GANCICLOVIR SODIUM

CYTOVENE Approval History

Loading approval history...

What CYTOVENE Treats

7 FDA approvals

Originally approved for its first indication in 1989 . Covers 7 distinct patient populations.

  • Other (7)
🔬

Active Pipeline

Pro

Ongoing clinical trials by development phase

Loading...

Key Completed Trials

Pro

Completed studies with published results, ranked by significance

Loading...
📊

Trial Timeline

Full development history with FDA approval milestones

Loading...
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.

CYTOVENE FDA Label Details

Pro

Want competitive intelligence?

See who's developing similar drugs and track their progress

View Pipeline Dashboard

Data Sources

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