Astagraf XLTreatment for Organ Transplant -- Rejection Prophylaxis
NDA for Immunosuppressant FK506 Modified Release Formulation Submitted in the US
TOKYO, December 26,2005 - Astellas Pharma US, Inc. (headquarters: Deerfield, Illinois; Chairman and CEO: Makoto Nishimura), a US subsidiary of Astellas Pharma Inc. ("Astellas"; headquarters: Tokyo; President and CEO: Toichi Takenaka), has submitted to the FDA an NDA for the immunosuppressant FK506 modified release formulation (generic name: tacrolimus) with the target indication of the prevention of organ rejection in patients receiving organ transplants.
Tacrolimus is an immunosuppressant invented by Astellas. It is marketed as an agent to suppress rejection after organ transplantations under the brand name of Prograf in over 70 countries in the world.
The FK506 modified release formulation is a modified release version of Prograf that can be administered once a day. Patients' compliance is thus expected to be improved compared to twice a day with the conventional formulation. The FK506 modified release formulation is therefore expected long term graft protective effect. In addition, this formulation is expected to be at least as safe as the conventional formulation since the peak blood concentration can be controlled at lower levels. It also makes it possible to optimize the dosage based on blood concentrations.
At present, application for regulatory approval is being prepared in Europe, while Phase II trials are underway in Japan.
Posted: December 2005
- Astellas Announces FDA Approval of Astagraf XL (tacrolimus extended-release capsules) for the Prophylaxis of Organ Rejection - July 22, 2013