Lifeline for severe bleeding disorder: drug access extended

NCT ID NCT06173024

First seen Jun 26, 2026 · Last updated Jun 26, 2026

Summary

This program provides continued compassionate access to recombinant von Willebrand factor (rVWF) for children and adults with severe von Willebrand disease who completed a prior study and are benefiting from treatment. Participants must have no comparable alternative therapy available. The goal is to prevent bleeding complications while no other options exist.

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance

recombinant von Willebrand factor (rVWF, TAK-577)

What this could lead to

If successful, this program ensures continued bleeding control for people with severe von Willebrand disease who have no other treatment options.

What could go wrong

This is an access program, not a new trial, so it does not test effectiveness or safety. Only a small number of eligible patients from one prior study can participate.

Disclaimer Read more

This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Conditions

The condition(s) this trial relates to.

hereditary von Willebrand disease von Willebrand disease (hereditary or acquired)

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••