drugset / Trial / NCT03588299

Study to Test the Safety and How Well Patients With Severe Hemophilia A Respond to Treatment With BAY 2599023 (DTX 201), a Drug Therapy That Delivers a Healthy Version of the Defective Factor VIII Gene Into the Nucleus of Liver Cells Using an Altered, Non-infectious Virus (AAV) as a "Shuttle"

NCT03588299 ↗

Phase 1/2 Active not recruiting 11 enrolled Bayer Ultragenix pharmaceutical · collab
NaSingle-groupOpen-labelTreatment

Summary

In this study researchers want to gather more information about safety and effectiveness of BAY 2599023 (DTX201), a drug therapy that delivers the human factor VIII gene into the human body by use of a viral vector to treat the disease. By replacing the defective gene with a healthy copy the human body may produce clotting factor on its own. Hemophilia A is a bleeding disorder in which the human body does not have enough clotting factor VIII, a protein that controls bleeding. Researcher want to find the optimal dose of BAY 2599023 (DTX201) so that the body may produce enough clotting factor on its own.

Timeline

Start
2018-11-07
Primary completion
2026-09-15
Completion
2026-09-15

Drugs

EvaluationDrugModalityDoseRoute
Subject BAY2599023 Gene therapy (AAV / viral vector) — Intravenous

Indications