Worldwide Hemophilia A and B Therapeutics in Asia-Pacific Markets Growth Driven by Increasing Treatmen to 2022

 

“The Report Hemophilia A and B Therapeutics in Asia-Pacific Markets to 2022 – Growth Driven by Increasing Treatment-Receiving Pool, Launch of Long-Acting Replacement Therapies and Non-factor Therapy provides information on pricing, market analysis, shares, forecast, and company profiles for key industry participants. – MarketResearchReports.biz”

Hemophilia is a rare disease affecting more than 400,000 people worldwide. Hemophilia A is four times as common as hemophilia B, and more than half of patients with hemophilia A have a severe form of hemophilia. Males have a much higher chance of developing hemophilia because they only receive one copy of the X chromosome from their mother.

The mainstay of treatment for hemophilia is to replace the missing factor VIII or factor IX, produced using plasma-derived or recombinant methods. Some patients develop inhibitors to factor VIII or factor IX treatment and need a bypassing agent, such as factor VIIa, 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 market opportunity.

The current marketed products landscape comprises replacement factor therapies, such as recombinant therapies and new long-acting recombinant products. The current pipeline shows strong promise, as it shows a gradual shift from short-acting recombinant factor VIII or factor IX to long-acting recombinant factor VIII, and from factor replacement therapies to non-factor therapies. Nevertheless, significant unmet need remains for products that can avoid the development of inhibitors in patients with hemophilia.

Though late-stage pipeline for treatment of hemophilia seems promising, the main market restraint is likely to be low penetration of new long-acting recombinant therapies in India and China, owing to their high expected prices.

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Scope

  • The Hemophilia A and B Asia-Pacific market will be valued at $699.1m and $112.9m respectively in 2022, growing from $444.9m and $76.3m in 2015, at compound annual growth rates of 6.7% and 5.8%.

  • How will non-factor therapies contribute to the growth?

  • What will be the impact of the new long-acting recombinant factor VIII and recombinant factor IX products in the hemophilia A and B market sales?

  • The pipeline contains a range of molecule types and molecular targets, including both those that are well established in hemophilia A and B, and novel targeted therapies.

  • Which molecular targets appear most frequently in the pipeline?

  • Will the pipeline address unmet needs such as less frequently administered therapies and risk of inhibitor development for hemophilia A and B patients?

  • What are the most promising first-in-class targets for hemophilia A and B?

  • Will the current first-in-class targets have a broader therapeutic potential across the Asia-Pacific markets?

  • Various drivers and barriers will influence the market over the forecast period.

  • What are the barriers that will limit the uptake of premium-priced recombinant factor VIII and recombinant factor IX therapies in the assessed countries?

  • Which factors are most likely to drive the market in these countries?

  • Co-development deals are the most common form of strategic alliance in hemophilia A and B, with total deal values ranging from under $10m to over $280m.

  • How do deal frequency and value compare between target families and molecule types?

  • What were the terms and conditions of key co-development deals?

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Reasons to buy

This report will allow you to –

  • Understand the current clinical and commercial landscape by considering disease pathogenesis, diagnosis, prognosis, and the treatment options available at each stage of diagnosis, including a clinical comparison of marketed therapies.

  • Visualize the composition of the hemophilia A and B market in terms of the dominant therapies for each patient subset, along with their clinical and commercial standing. Unmet needs are highlighted to allow a competitive understanding of gaps in the current market.

  • Analyze the hemophilia A and B pipeline and stratify pipeline therapies by stage of development, molecule type and molecular target. There are promising signs in the pipeline that the industry is seeking novel approaches to treating hemophilia A and B.

  • Understand the potential of late-stage therapies, with extensive profiles of products that could enter the market over the forecast period, highlighting clinical performance, potential commercial positioning, and how they will compete with other therapies.

  • Predict hemophilia A and B market growth in the five Asia-Pacific markets with epidemiological and annual cost of therapy forecasts across India, China, Australia, South Korea and Japan, as well as individual contributions of promising late-stage molecules to market growth.

  • Identify commercial opportunities in the hemophilia A and B deals landscape by analyzing trends in licensing and co-development deals.

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Table of Contents

1 Table of Contents

1 Table of Contents 5

1.1 List of Tables 8

1.2 List of Figures 9

2 Introduction 11

2.1 Disease Introduction 11

2.2 Epidemiology 12

2.3 Symptoms 12

2.4 Etiology and Pathophysiology 13

2.4.1 Hemophilia A 13

2.4.2 Hemophilia B 13

2.5 Diagnosis 14

2.6 Diagnosis of Inhibitors 14

2.7 Disease stages 15

2.8 Prognosis 15

2.9 Treatment Options 15

2.9.1 Management of Bleeding with Factor Replacement Therapy 16

2.9.2 Antifibrinolytic Medication 18

3 Marketed Products 21

3.1 Overview 21

3.2 Marketed Products – Hemophilia A 21

3.2.1 Advate (octacog alfa) – Baxalta 21

3.2.2 Adynovate (rurioctocog alfa pegol) – Baxalta 23

3.2.3 Xyntha/ReFacto AF (moroctocog alfa) – Pfizer 24

3.2.4 Kogenate FS (octacog alfa) – Bayer 25

3.2.5 Kovaltry (octacog alfa) – Bayer 26

3.2.6 Eloctate (efmoroctocog Alfa) – Biogen 28

3.2.7 Nuwiq (simoctocog alfa) – Octapharma 29

3.2.8 NovoEight (turoctocog alfa) – Novo Nordisk 30

3.2.9 GreenGene F (Beroctocog Alfa) – Green Cross 32

3.3 Marketed Products – Hemophilia B 33

3.3.1 Alprolix (Eftrenonacog alfa) – Biogen 33

3.3.2 BeneFix (nonacog alfa) – Pfizer 34

3.3.3 Rixubis (nonacog gamma) – Baxter 36

3.3.4 Idelvion (albutrepenonacog alfa) – CSL Behring 36

3.4 Marketed Products – Hemophilia A and B 38

3.4.1 Feiba NF (anti-inhibitor coagulant complex) – Baxter 38

3.4.2 Byclot (freeze-dried-activated human blood coagulation factor VII concentrate containing factor X) – Kaketsuken 39

3.5 Comparative Efficacy and Safety of Marketed Products 40

4 Pipeline Analysis 42

4.1 Overview 42

4.2 Pipeline by Stage of Development, Molecule Type, Route of Administration and Program Type 42

4.3 Pipeline by Molecular Target 44

4.4 Promising Pipeline Candidates – Hemophilia A 45

4.4.1 BAX-801 (susoctocog alfa) – Baxalta 45

4.4.2 CSL-627/NBP-601 (Lonoctocog alfa) – CSL Behring 47

4.4.3 Emicizumab (ACE-910/RG6013) – Roche 49

4.4.4 N8-GP (turoctocog Alfa Pegol) – Novo Nordisk 51

4.4.5 BAY94-9027 (damoctocog alfa pegol) – Bayer 53

4.5 Promising Pipeline Candidates -Hemophilia B 55

4.5.1 N9-GP/NN-7999 (nonacog beta pegol) – Novo Nordisk 55

4.6 Promising Pipeline Candidates -Hemophilia A and B 57

4.6.1 BAX-817 (recombinant activated factor VII BI) – Baxalta 57

4.6.2 CSL-689 (recombinant activated VII-FP) – CSL Behring 58

4.7 Comparative Efficacy and Safety of Pipeline Products 59

4.8 Product Competitiveness Framework 60

5 Clinical Trial Analysis 63

5.1 Failure Rate 63

5.1.1 Overall Failure Rate 63

5.1.2 Failure Rate by Phase and Molecule Type 64

5.1.3 Failure Rate by Phase and Molecular Target 64

5.2 Clinical Trial Duration 65

5.2.1 Clinical Trial Duration by Molecule Type 65

5.2.2 Clinical Trial Duration by Molecular Target 66

5.3 Clinical Trial Size 67

5.3.1 Patient Enrollment per Product by Molecule Type, Molecular Target and Stage of Development 67

5.3.2 Patient Enrollment per Trial by Molecule Type, Molecular Tar

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