TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

VEREGEN

SINECATECHINS
Immunology Approved 2006-10-31
2
Indications
--
Phase 3 Trials
19
Years on Market

Details

Status
Prescription
First Approved
2006-10-31
Routes
TOPICAL
Dosage Forms
OINTMENT

Companies

Active Ingredient: SINECATECHINS

VEREGEN Approval History

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What VEREGEN Treats

2 indications

VEREGEN is approved for 2 conditions since its original approval in 2006. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Genital Warts
  • Perianal Warts
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.

VEREGEN FDA Label Details

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Indications & Usage

FDA Label (PDF)

Veregen is a topical ointment indicated for the treatment of external genital and perianal warts (Condylomata acuminata) in immunocompetent patients 18 years and older . Limitations of Use Safety and effectiveness of Veregen have not been established in immunosuppressed patients, in treatment of external genital and perianal warts beyond 16-weeks, or for multiple treatment courses . 1.1 Indication Veregen is indicated for the topical treatment of external genital and perianal warts (Condylomata acuminata) in immunocompetent patients 18 years and older. 1.2 Limitations of Use The safety and eff...

VEREGEN Patents & Exclusivity

Latest Patent: Oct 2026

Patents (1 active)

US7858662 Expires Oct 2, 2026
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.