TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

VALRUBICIN

VALRUBICIN
Oncology Approved 2019-04-19
1
Indication
--
Phase 3 Trials
6
Years on Market

Details

Status
Prescription
First Approved
2019-04-19
Routes
INTRAVESICAL
Dosage Forms
SOLUTION

Companies

Active Ingredient: VALRUBICIN

VALRUBICIN Approval History

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What VALRUBICIN Treats

1 indications

VALRUBICIN is approved for 1 conditions since its original approval in 2019. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Carcinoma In Situ of the Urinary Bladder
Source: FDA Label

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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.

VALRUBICIN FDA Label Details

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Indications & Usage

Valrubicin intravesical solution is an anthracycline topoisomerase inhibitor indicated for intravesical therapy of BCG-refractory carcinoma in situ (CIS) of the urinary bladder in patients for whom immediate cystectomy would be associated with unacceptable morbidity or mortality. • Valrubicin intravesical solution is an anthracycline topoisomerase inhibitor indicated for intravesical therapy of BCG-refractory carcinoma in situ (CIS) of the urinary bladder in patients for whom immediate cystectomy would be associated with unacceptable morbidity or mortality.

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Data Sources

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