TheraRadar
Data updated: May 26, 2026

Vonvendi (von willebrand factor (recombinant))

Approved 2015-12-07
Jump to: Indications Approvals Trials Competitors Safety Patents
1
Indication
--
Phase 3 Trials
10
Years on Market

Details

Status
Prescription
First Approved
2015-12-07
Patent Cliff
2029

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Routes
Intravenous
Dosage Forms
For Injection

Companies

Takeda
Active Ingredient: von Willebrand factor (Recombinant) , von Willebrand factor (Recombinant)

Vonvendi Approval History

2016
2017
2018
2019
2020
2021
2022
2023
2024
2025
2026
Original
New Indication
New Form
Label Update
1 FDA actions from 2015 to 2015
Dec 2015 ORIGINAL
Update · CBER biologic (Purple Book)

What Vonvendi Treats

1 FDA approvals

Originally approved for its first indication in 2015 .

  • Other (1)
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Clinical Trial Registry

2 trials
Trial Sponsor ID Phase Status Title
NCT07129343 TAK-577-3002 Ph 3 recruiting A Study of Recombinant Von Willebrand Factor (rVWF) in Chinese Participants With Von Willebrand Disease (vWD)
NCT02973087 results posted 071301 2016-001478-14 Ph 3 completed rVWF IN PROPHYLAXIS
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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

ClinicalTrials.gov ↗ Pro

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.

Vonvendi FDA Label Details

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Data Sources

FDA Approval: BLA125577 → Trials: ClinicalTrials.gov →

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