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BAY14-2222_Kogenate-FS FVIII

Bayer · Phase 2 active Biologic

BAY14-2222_Kogenate-FS FVIII is a Factor VIII replacement therapy Biologic drug developed by Bayer. It is currently in Phase 2 development for Hemophilia A.

Factor VIII replacement therapy

Factor VIII replacement therapy Used for Hemophilia A.

At a glance

Generic nameBAY14-2222_Kogenate-FS FVIII
SponsorBayer
Drug classFactor VIII replacement therapy
TargetFactor VIII
ModalityBiologic
Therapeutic areaHematology
PhasePhase 2

Mechanism of action

BAY14-2222_Kogenate-FS FVIII is a recombinant human coagulation factor VIII used to treat hemophilia A.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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Frequently asked questions about BAY14-2222_Kogenate-FS FVIII

What is BAY14-2222_Kogenate-FS FVIII?

BAY14-2222_Kogenate-FS FVIII is a Factor VIII replacement therapy drug developed by Bayer, indicated for Hemophilia A.

How does BAY14-2222_Kogenate-FS FVIII work?

Factor VIII replacement therapy

What is BAY14-2222_Kogenate-FS FVIII used for?

BAY14-2222_Kogenate-FS FVIII is indicated for Hemophilia A.

Who makes BAY14-2222_Kogenate-FS FVIII?

BAY14-2222_Kogenate-FS FVIII is developed by Bayer (see full Bayer pipeline at /company/bayer).

What drug class is BAY14-2222_Kogenate-FS FVIII in?

BAY14-2222_Kogenate-FS FVIII belongs to the Factor VIII replacement therapy class. See all Factor VIII replacement therapy drugs at /class/factor-viii-replacement-therapy.

What development phase is BAY14-2222_Kogenate-FS FVIII in?

BAY14-2222_Kogenate-FS FVIII is in Phase 2.

What are the side effects of BAY14-2222_Kogenate-FS FVIII?

Common side effects of BAY14-2222_Kogenate-FS FVIII include Headache, Nausea, Fatigue.

What does BAY14-2222_Kogenate-FS FVIII target?

BAY14-2222_Kogenate-FS FVIII targets Factor VIII and is a Factor VIII replacement therapy.

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