prophylaxis of Bleeding (DBCOND0020314)

Identifiers

Synonyms
Prophylaxis of bleeding episodes

Associated Data

Indicated Drugs and Targets
DrugDescriptionTargets
Albutrepenonacog alfa
A recombinant Factor IX fused to recombinant human albumin used to treat hemophilia B.
Antihemophilic factor (recombinant), PEGylated
For the management of hemophilia A (congenital factor VIII deficiency) [FDA label], . This medication is a human antihemophilic factor indicated in adolescent and adult patients (12 years and older)...
Antihemophilic factor, human recombinant
A form of recombinant coagulation Factor VIII used to treat hemophilia A, von Willebrand disease, and Factor XIII deficiency.
Catridecacog
A recombinant FXIII subunitā€A molecule evaluated for clotting factor replacement therapy in congenital FXIII deficiency.
Coagulation Factor IX (Recombinant)
A form of recombinant human coagulation Factor IX used to treat hemophilia B.
Coagulation factor X human
A coagulation factor used to treat Factor X deficiency to control bleeding.
No drug targets
Desmopressin
A synthetic analog of vasopressin used to reduce renal excretion of water in central diabetes insipidus and nocturia.
Efanesoctocog alfa
A recombinant DNA-derived, Factor VIII concentrate indicated for routine prophylaxis, on-demand treatment and control of bleeding episodes, and perioperative management of bleeding in patients with hemophilia A.
Efmoroctocog alfa
A recombinant Factor VIII used to treat and prevent bleeding in hemophilia A.
Factor IX Complex (Human)
A Factor IX complex used to prevent and treat bleeding episodes in hemophilia B or vitamin K antagonist therapy.
No drug targets
Lonoctocog alfa
A recombinant Factor VIII used to treat hemophilia A to control bleeding.
Turoctocog alfa
An antihemorrhagic agent used for the treatment and prophylaxis of bleeding in patients of all ages with haemophilia A (congenital factor VIII deficiency).
Von Willebrand factor human
A blood clotting factor used to manage bleeding episodes in von Willebrand disease and hemophilia A.
Clinical Trials
IdentifierTitleDrug(s)PurposePhaseStatus
NCT05036278
Prophylaxis Regimen for Hemophilia A Patientstreatment4active_not_recruiting
NCT05147662
A Study to Learn How Safe the Study Treatment BAY94-9027 is and How it Affects the Body in Previously Treated Children Aged 7 to Less Than 12 Years With Severe Hemophilia A, a Genetic Bleeding Disorder That is Caused by the Lack of a Protein Called Clotting Factor 8 (FVIII) in the Bloodtreatment3active_not_recruiting
NCT06222697
A Study to Learn More About the Safety of Damoctocog-alfa-pegol When Used in Routine Medical Care in Korean Participants With Hemophilia ANot AvailableNot Availablerecruiting
NCT05643560
An Observational Study Called JOIHA to Learn More About How Well the Treatment With Jivi Works to Prevent Problems With Joints in Adults With Hemophilia ANot AvailableNot Availablerecruiting