Hemophilia A and B Recombinant Factor Replacement Therapy - US Drug Forecast and Market Analysis to 2024

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Hemophilia A and B Recombinant Factor Replacement Therapy - US
Drug Forecast and Market Analysis to 2024
Summary
Congenital Hemophilia A and B are bleeding disorders that are caused by genetic X-linked deficiencies in
the blood clotting Factors VIII and IX, respectively. Hemophilia manifests as mild, moderate, or severe
inability to form clots, depending upon the endogenous levels of circulating factor in an individual patient.
The mainstay of treatment for hemophilia is to replace the missing FVIII or FIX, produced using plasmaderived or recombinant methods. Some patients develop inhibitors to FVIII or FIX treatment and need a
bypassing agent, such as FVIIa, to resolve bleeds. Patients of hemophilia A or B often require lifelong
treatment to prevent and control bleeding episodes, and this therefore represents a lucrative sales
opportunity.
The US is the largest global hemophilia market, due to high rates of disease diagnosis combined with high
rates of primary rFVIII and rFIX prophylaxis among diagnosed severe hemophilia A and B patients. This
market growth will be driven by increasing rates of prevalent cases of hemophilia A and B, and increasing
uses of recombinant replacement factors in hemophilia A and B patients over the forecast period.
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Scope
- Overview of Hemophilia A and B including epidemiology, etiology, symptoms, diagnosis, pathology and
treatment guidelines as well as an overview on the competitive landscape.
- Detailed information on the key drugs in the US including product description, safety and efficacy profiles
as well as a SWOT analysis.
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- Sales forecast for the top drugs in the US from 2014-2024.
- Analysis of the impact of key events as well the drivers and restraints affecting the US Hemophilia A and
B market.
Reasons to buy
- Understand and capitalize by identifying products that are most likely to ensure a robust return
- Stay ahead of the competition by understanding the changing competitive landscape for Hemophilia A
and B.
- Effectively plan your M&A and partnership strategies by identifying drugs with the most promising sales
potential
- Make more informed business decisions from insightful and in-depth analysis of drug performance
- Obtain sales forecast for drugs from 2014-2024 in US.
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Table of Content
1 Table of Contents
1.1 List of Tables
1.2 List of Figures
2 Introduction
2.1 Catalyst
2.2 Related Reports
2.3 Upcoming Related Reports
3 Disease Overview
3.1 Etiology and Pathophysiology
3.1.1 Etiology
3.1.2 Pathophysiology
3.1.3 Prognosis and Quality of Life
3.2 Symptoms
3.2.1 Hemophilia A and B
3.2.2 Inhibitors
4 Disease Management
4.1 Treatment Overview
4.1.1 Hemophilia A and B Diagnosis
4.1.2 Hemophilia A and B Treatment
4.1.3 Diagnosis of Inhibitors
4.1.4 Treatment of Inhibitors
4.2 US
4.2.1 Clinical Practice
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Connect for more details:
Sam Collins
Market Reports Center
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info@marketreportscenter.com

Congenital Hemophilia A and B are bleeding disorders that are caused by genetic X-linked deficiencies in the blood clotting Factors VIII and IX, respectively. Hemophilia manifests as mild, moderate, or severe inability to form clots, depending upon the endogenous levels of circulating factor in an individual patient.