Efficacy, safety and pharmaco-economic assessment ofsecondary long term prophylaxis with highly purified, standardized, doubly virus inactivated FVIII/VWF concentrates in patients with severe, inherited VWDand frequent bleedings - PRO.WILL.

Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico0 sites24 target enrollmentMay 21, 2013

Overview

Phase: Phase 1
Intervention: Not specified
Conditions: Patients with severe, inherited Von Willebrand’s disease and frequent bleedings
Sponsor: Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico
Enrollment: 24
Status: Active, not recruiting
Last Updated: 9 years ago

No summary available.

Registry

who.int

Start Date

May 21, 2013

End Date

TBD

Last Updated

9 years ago

Study Type

Interventional clinical trial of medicinal product

Sex

All

Sponsor

Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico

•Patients \=6 years old
•Documented unresponsiveness to DDAVP. All the patients, excluding type 3 and type 2B, should have been exposed to a documented infusion trial with DDAVP. Responsiveness to DDAVP is defined as an increase in plasma FVIII:C and VWF:RCo levels of at least three fold over baseline and in absolute reaching at least 30 IU/dl for both values
•contraindication to DDAVP (namely type 2B VWD patients or other patients who display significant side effects to DDAVP)
•\-Frequent, spontaneous bleedings i.e. at least 5 episodes in whatever anatomical site in the last 12 months, (unless patients currently under prophylaxis with VWF/FVIII concentrates; see below) severe enough to require treatment with FVIII/VWF concentrates
•Prolonged or excess bleeding during menses will be allowed only when:
•i.No other medication can control frequent bleeds
•ii.Bleeding exceeds 10 consecutive days
•Recurrent spontaneous bleedings, severe enough to require treatment with FVIII/VWF concentrates of the following types:
•?Epistaxes (at least 5 episodes in the last 12 months)
•?Hemarthroses (at least 3 episodes at the same joint in the last 12 months)

•\-a life expectancy \< 1 year
•\-presence of alloantibodies to VWF or FVIII
•\-acquired Von Willebrand’s syndrome (AVWS)
•\-co\-morbidity with other haemorrhagic diathesis, excluded those linked to VWD as the complication of treatment (for instance thrombocytopenia in Type 2B VWD)
•\-advanced liver cirrhosis with:
•?cirrhosis related coagulation abnormalities (thrombocytopenia, defined as platelet count \< 50\.000/mm3, INR \>1,7, prolonged prothrombin time \> 4 seconds versus normal)
•?portal hypertension with history of variceal bleeding
•\-pregnancy and lactation
•\-any known need for invasive procedures or elective surgery scheduled in the following 3 months (recruitment in these cases should be postponed)
•\-proven co\-morbidity for other causes of gastrointestinal bleeding not related to the studied disease (as drug induced haemorrhagic gastropathy, upper GI tract ulcers or cancer, or operable conditions, e.g. haemorrhoids) with the exception of concomitant angiodysplasia which meets the inclusion criteria