Coagulation Factor Deficiency Market - US to Have the Lion's Share Among the 7MM's

The market for coagulation factor deficiency treatments is experiencing robust growth, driven by advancements in biotechnology and the increasing prevalence of bleeding disorders. Innovations in therapeutic options and improved patient access to healthcare contribute to the expanding coagulation factor deficiency market landscape.

LAS VEGAS, July 10, 2024 /PRNewswire/ -- DelveInsight's Coagulation Factor Deficiency Market Insights report includes a comprehensive understanding of current treatment practices, coagulation factor deficiency emerging drugs, market share of individual therapies, and current and forecasted market size from 2020 to 2034, segmented into 7MM [the United States, the EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan].

Key Takeaways from the Coagulation Factor Deficiency Market Report

According to DelveInsight's analysis, the market size for coagulation factor deficiency was found to be USD 13.5 billion in the 7MM in 2023.
The total 7MM prevalent cases of coagulation factor deficiency in 2023 were 105K out of which the highest prevalent cases were estimated in the United States.
Leading coagulation factor deficiency companies such as Novo Nordisk, Spark Therapeutics, Sanofi (Genzyme), Alnylam Pharmaceuticals, Pfizer, Biotest AG, Centessa Pharmaceuticals (Apcintex), Staidson Biopharma Inc., Ultragenyx Pharmaceutical, Bayer, and others are developing novel coagulation factor deficiency drugs that can be available in the coagulation factor deficiency market in the coming years.
The promising coagulation factor deficiency therapies in the pipeline include Concizumab (NN7415), RG6357 (SPK-8011), Fitusiran (ALN-AT3, SAR-439774), Marstacimab (PF-06741086), NNC0365-3769 A (MIM8), BT524, SERPINPC, STSP-0601, BAY2599023 (DTX201 AAV FVIII), and others.
In March 2024, ReciBioPharm signed a collaboration agreement with GeneVentiv Therapeutics, a preclinical gene therapy company, to advance the development of an adeno-associated virus (AAV)-based universal gene therapy for hemophilia, and reportedly the first to treat hemophilia patients with inhibitors.
In June 2023, the FDA accepted the company's BLA for fidanacogene elaparvovec for the treatment of adults with hemophilia B. In parallel, the European marketing authorization application (MAA) for fidanacogene elaparvovec has also been accepted and is under review by the European Medicines Agency (EMA).
In May 2023, Novo Nordisk notified the National Hemophilia Foundation that they had received a Complete Response Letter (CRL) from the US Food and Drug Administration (FDA) for their investigational, subcutaneous therapy concizumab. While Novo Nordisk had anticipated potential FDA approval of the therapy in the Spring of 2023, the additional information outlined in the CRL will stretch that timeline.

Discover which therapies are expected to grab the major coagulation factor deficiency market share @ Coagulation Factor Deficiency Market Report

Coagulation Factor Deficiency Overview

Coagulation factor deficiency diseases, also referred to as bleeding or clotting disorders, encompass a range of inherited or acquired conditions marked by the absence or malfunction of specific proteins essential for blood clotting. These proteins, known as coagulation factors, are vital for stopping bleeding by forming clots to close injured blood vessels.

There are several coagulation factors, labeled from I to XIII, that function in a complex and coordinated way to achieve hemostasis. Deficiencies in any of these factors can cause abnormal bleeding, varying in severity from mild to severe, depending on the specific factor affected and the extent of the deficiency.

Blood disorders are typically diagnosed by examining a range of symptoms and conducting various blood tests, which differ depending on the specific factor involved. Coagulation factor I deficiency is generally identified through a series of blood tests that measure the amount of fibrinogen in the blood. However, a low fibrinogen level can sometimes indicate liver or kidney disorders. For coagulation factor II, diagnosis is usually made using prothrombin time (PT) and partially activated thromboplastin time (aPTT) tests. Deficiency levels can range from 2% to 50% of normal, with patients at or near 50% usually experiencing normal or no bleeding issues.

Coagulation Factor Deficiency Epidemiology Segmentation

The coagulation factor deficiency epidemiology section provides insights into the historical and current coagulation factor deficiency patient pool and forecasted trends for the 7MM. It helps recognize the causes of current and forecasted patient trends by exploring numerous studies and views of key opinion leaders.

The coagulation factor deficiency market report proffers epidemiological analysis for the study period 2020–2034 in the 7MM segmented into:

Total Coagulation Factor Deficiency Diagnosed Prevalent Cases
Factor-Specific Coagulation Factor Deficiency Prevalent Cases

Coagulation Factor Deficiency Treatment Market

The treatment of coagulation factor deficiency typically involves replacing the missing factor in the blood, supplemented by additional therapies when bleeding persists. There are several treatments available for managing coagulation factor deficiencies. For moderate conditions like mucosal tract hemorrhage or heavy menstruation, physicians often prescribe antifibrinolytic drugs and hormones. Discovered after 1950, therapies such as Aminocaproic acid (EACA) and tranexamic acid (TA) help stabilize clots in areas like the mouth, bladder, and uterus. These adjunctive therapies are also beneficial for dental surgeries but are less effective for internal bleeding. These medications can be administered orally or by injection.

ESPEROCT (Turoctocog alfa pegol, also known as N8-GP) is an extended half-life glycopegylated factor VIII molecule used for routine prophylaxis to reduce the frequency of bleeding episodes, on-demand treatment and control of bleeding episodes, and perioperative management of bleeding.

This product has been evaluated in five prospective, multi-center clinical trials involving previously treated patients with severe hemophilia A and no history of inhibitors. The results of these trials have shown that the overall safety profile of ESPEROCT is comparable to other long-acting FVIII products, with no safety concerns identified after more than 5 years of clinical exposure.

JIVI (antihemophilic factor [recombinant] PEGylated-aucl), developed by Bayer, is designed for previously treated adults and adolescents (12 years and older) with hemophilia A (congenital Factor VIII deficiency). It is used for:

On-demand treatment and control of bleeding episodes
Perioperative management of bleeding
Routine prophylaxis to reduce the frequency of bleeding episodes.

JIVI functions by replacing the deficient or absent factor VIII (FVIII) in patients with hemophilia A. It is also known as Damoctocog alfa pegol.

To know more about coagulation factor deficiency treatment guidelines, visit @ Coagulation Factor Deficiency Management

Coagulation Factor Deficiency Pipeline Therapies and Key Companies

Concizumab (NN7415): Novo Nordisk
RG6357 (SPK-8011): Roche (Spark Therapeutics)
Fitusiran (ALN-AT3, SAR-439774): Sanofi (Genzyme)/Alnylam Pharmaceuticals
Marstacimab (PF-06741086): Pfizer
NNC0365-3769 A (MIM8): Novo Nordisk A/S
BT524: Biotest AG
SERPINPC: Centessa Pharmaceuticals (Apcintex)
STSP-0601: Staidson Biopharma Inc.
BAY2599023 (DTX201 AAV FVIII): Bayer/Ultragenyx Pharmaceutical

Discover more about coagulation factor deficiency drugs in development @ Coagulation Factor Deficiency Clinical Trials

Coagulation Factor Deficiency Market Dynamics

The coagulation factor deficiency market dynamics are expected to change in the coming years. The coagulation factor deficiency market is primarily driven by several key factors. The increasing prevalence of hemophilia and other bleeding disorders is a significant driver, as these conditions require ongoing management and treatment with coagulation factor concentrates. Advances in biotechnology have led to the development of novel therapies, such as recombinant and plasma-derived coagulation factors, which offer improved safety and efficacy profiles, further stimulating market growth.

Additionally, rising awareness about bleeding disorders and the importance of early diagnosis and treatment has led to increased demand for coagulation factor products. Government initiatives and support for rare disease treatment, along with favorable reimbursement policies, are also contributing to market expansion. Moreover, ongoing research and development activities aimed at discovering new treatments and improving existing ones are expected to create lucrative opportunities in the market.

Furthermore, potential therapies are being investigated for the treatment of coagulation factor deficiency, and it is safe to predict that the treatment space will significantly impact the coagulation factor deficiency market during the forecast period. Moreover, the anticipated introduction of emerging therapies with improved efficacy and a further improvement in the diagnosis rate are expected to drive the growth of the coagulation factor deficiency market in the 7MM.

However several factors may impede the growth of the coagulation factor deficiency market. One of the primary challenges is the high cost of treatment, particularly with recombinant and plasma-derived therapies, which limits accessibility for many patients. Additionally, there is a lack of awareness and diagnosis in many regions, particularly in low-income and rural areas, which leads to underdiagnosis and undertreatment of these conditions.

Regulatory hurdles also pose a significant barrier, as the approval process for new therapies is often lengthy and stringent, delaying the availability of potentially life-saving treatments. Furthermore, the coagulation factor deficiency market is constrained by limited research and development funding, which impedes the discovery of innovative therapies. Lastly, the logistical challenges associated with the storage and distribution of these specialized products, which often require cold chain logistics, add another layer of complexity to coagulation factor deficiency market penetration and access.

Coagulation Factor Deficiency Market Report Metrics	Details
Study Period	2020–2034
Coverage	7MM [the United States, the EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan].
Coagulation Factor Deficiency Market Size	USD 13.5 Billion
Key Coagulation Factor Deficiency Companies	Novo Nordisk, Spark Therapeutics, Sanofi, Alnylam Pharmaceuticals, Pfizer, Biotest AG, Centessa Pharmaceuticals (Apcintex), Staidson Biopharma Inc., Ultragenyx Pharmaceutical, Bayer, and others
Key Pipeline Coagulation Factor Deficiency Therapies	Concizumab (NN7415), RG6357 (SPK-8011), Fitusiran (ALN-AT3, SAR-439774), Marstacimab (PF-06741086), NNC0365-3769 A (MIM8), BT524, SERPINPC, STSP-0601, BAY2599023 (DTX201 AAV FVIII), and others

Scope of the Coagulation Factor Deficiency Market Report

Therapeutic Assessment: Coagulation Factor Deficiency current marketed and emerging therapies
Coagulation Factor Deficiency Market Dynamics: Key Market Forecast Assumptions of Emerging Coagulation Factor Deficiency Drugs and Market Outlook
Competitive Intelligence Analysis: SWOT analysis and Market entry strategies
Unmet Needs, KOL's views, Analyst's views, Coagulation Factor Deficiency Market Access and Reimbursement

Download the report to understand which factors are driving coagulation factor deficiency market trends @ Coagulation Factor Deficiency Market Trends

Table of Contents

1	KEY INSIGHTS
2	REPORT INTRODUCTION
3	COAGULATION FACTOR DEFICIENCY MARKET OVERVIEW AT A GLANCE
3.1	MARKET SHARE (%) DISTRIBUTION OF COAGULATION FACTOR DEFICIENCY IN 2020
3.2	MARKET SHARE (%) DISTRIBUTION OF COAGULATION FACTOR DEFICIENCY IN 2034
4	EXECUTIVE SUMMARY OF COAGULATION FACTOR DEFICIENCY
5	KEY EVENTS
6	EPIDEMIOLOGY AND MARKET METHODOLOGY
7	COAGULATION FACTOR DEFICIENCY DISEASE – OVERVIEW
7.1	INTRODUCTION
7.2	PROCESS OF CLOTTING
7.3	TYPE OF CLOTTING FACTORS AND THEIR FUNCTIONS
7.4	MECHANISM
7.5	TYPE OF COAGULATION FACTOR DEFICIENCY
7.5.1	Coagulation Factor I Deficiency (Fibrinogen)
7.5.1.1	Afibrinogenemia
7.5.1.2	Hypofibrinogenemia
7.5.1.3	Dysfibrinogeneima
7.5.1.4	Hypodysfibrinogenemia
7.5.2	Coagulation Factor II Deficiency (Prothrombin)
7.5.3	Coagulation Factor V Deficiency
7.5.4	Coagulation Factor VII Deficiency
7.5.5	Coagulation Factor VIII Deficiency (Hemophilia A)
7.5.6	Coagulation Factor IX Deficiency (Hemophilia B)
7.5.7	Coagulation Factor X Deficiency
7.5.8	Coagulation Factor XI Deficiency (Hemophilia C)
7.5.9	Coagulation Factor XII Deficiency
7.5.10	Coagulation Factor XIII Deficiency
7.5.11	Von Willebrand Disease
7.6	SYMPTOMS ASSOCIATED WITH DEFICIENCY OF COAGULATION FACTORS
7.7	CAUSES OF COAGULATION FACTOR DEFICIENCY DISEASE
7.7.1	Inherited (Genetic) Causes:
7.7.2	Acquired Causes:
7.8	TESTING
7.9	DIAGNOSIS
7.9.1	Diagnosis of Hemophilia A
7.9.1.1	Establishing the Diagnosis
7.9.1.2	Molecular Genetic Testing
7.9.1.3	Screening Tests
7.9.1.4	Clotting Factor Tests
7.9.1.5	Inhibitor Testing
7.9.2	Diagnosis of Hemophilia B
7.9.3	Diagnosis of Von Willebrand disease
7.1	TREATMENT AND MANAGEMENT
7.10.1	Treatment
7.10.1.1	Non replacement therapies
7.10.1.2	Replacement therapies
7.10.2	Management
7.10.2.1	Healthy lifestyle
7.10.2.2	Dental care
7.10.2.3	Vaccinations
7.10.2.4	Disease management in the case of females
8	EPIDEMIOLOGY AND PATIENT POPULATION
8.1	ASSUMPTIONS AND RATIONALE: 7MM
8.2	KEY FINDINGS
8.3	Total Diagnosed Prevalence of Coagulation Factor Deficiency in the 7mm
8.4	Factor-Specific Prevalence of Coagulation Factor Deficiency in the 7mm
8.5	THE UNITED STATES
8.5.1	Total Diagnosed Prevalence of Coagulation Factor Deficiency in the United States
8.5.2	Factor-specific Prevalence of Coagulation Factor Deficiency in the United States
8.6	EU4 AND THE UK
8.6.1	Total Diagnosed Prevalence of Coagulation Factor Deficiency in the EU4 and the UK
8.6.2	Factor-specific Prevalence of Coagulation Factor Deficiency in the EU4 and the UK
8.7	JAPAN
8.7.1	Total Diagnosed Prevalence of Coagulation Factor Deficiency in the Japan
8.7.2	Factor-specific Prevalence of Coagulation Factor Deficiency in the Japan
9	PATIENT JOURNEY
10	MARKETED THERAPIES
10.1	KEY CROSS
10.2	ESPEROCT (N8-GP; TUROCTOCOG ALFA PEGOL): NOVO NORDISK
10.2.1	Product Description
10.2.2	Regulatory Milestones
10.2.3	Other Developmental Activities
10.2.4	RecentClinical Development
10.2.4.1	Clinical Trials Information
10.2.5	Safety and efficacy
10.2.5.1	Summary of Pivotal Trials
10.2.6	Product Profile
10.3	JIVI (FORMERLY BAY94-9027): BAYER
10.3.1	Product Description
10.3.2	Regulatory Milestones
10.3.3	Other Developmental Activities
10.3.4	Recent Clinical Development
10.3.4.1	Clinical Trials Information
10.3.5	Safety and efficacy
10.3.5.1	Summary of Pivotal Trials
10.3.6	Product Profile
10.4	WILATE: OCTAPHARMA
10.4.1	Product Description
10.4.2	Regulatory Milestones
10.4.3	Recent Clinical Development
10.4.3.1	Clinical Trials Information
10.4.4	Safety and Efficacy
10.4.4.1	Summary of Pivotal Trials
10.4.5	Product Profile
10.5	ADYNOVATE (ADYNOVI; BAX 855): TAKEDA
10.5.1	Product Description
10.5.2	Regulatory Milestones
10.5.3	Other Developmental Activities
10.5.4	Recnt Clinical Development
10.5.4.1	Clinical Trials Information
10.5.5	Safety and efficacy
10.5.5.1	Summary of Pivotal Trials
10.5.6	Product Profile
10.6	ELOCTATE [ELOCTA (EFMOROCTOCOG ALFA)]: SANOFI/SOBI
10.6.1	Product Description
10.6.2	Regulatory Milestones
10.6.3	Other Developmental Activities
10.6.4	Safety and efficacy
10.6.4.1	Summary of Pivotal Trials
10.6.5	Product Profile
10.7	AFSTYLA (LONOCTOCOG ALFA): CSL BEHRING
10.7.1	Product Description
10.7.2	Regulatory Milestones
10.7.3	Other Developmental Activities
10.7.4	Safety and efficacy
10.7.4.1	Summary of Pivotal Trials
10.7.5	Product Profile
10.8	NUWIQ (SIMOCTOCOG ALFA): OCTAPHARMA
10.8.1	Product Description
10.8.2	Regulatory Milestone
10.8.3	Other Developmental Activities
10.8.4	Safety and Efficacy
1.1.1.1	Summary of Pivotal Clinical trial
10.8.5	Product Profile
10.9	KOVALTRY (BAY 81-8973): BAYER
10.9.1	Product Description
10.9.2	Regulatory Milestone
10.9.3	Other Developmental Activity
10.9.4	Safety and Efficacy
10.9.4.1	Summary of Pivotal Clinical Trial
10.9.5	Product Profile
10.10	OBIZUR: TAKEDA
10.10.1	Product Description
10.10.2	Regulatory Milestones
10.10.3	Other Developmental Activities
10.10.4	Recent Clinical Development
10.10.4.1	Clinical trials information
10.10.5	Safety and Efficacy
10.10.5.1	Summary of Pivotal Trials
10.10.6	Product Profile
10.11	KOGENATE FS (OCTOCOG ALFA): BAYER
10.11.1	Product Description
10.11.2	Regulatory Milestones
10.11.3	Other Developmental Activities
10.11.4	Safety and Efficacy
10.11.4.1	Summary of Pivotal Trials
10.11.5	Product Profile
10.12	XYNTHA (REFACTO AF): PFIZER
10.12.1	Product Description
10.12.2	Regulatory Milestones
10.12.3	Other Developmental Activities
10.12.4	Safety and Efficacy
10.12.4.1	Summary of Pivotal Trials
10.12.5	Product Profile
10.13	FEIBA: TAKEDA
10.13.1	Product Description
10.13.2	Regulatory Milestones
10.13.3	Other Developmental Activities
10.13.4	Recent Clinical Developmen
10.13.4.1	Clinical trials information
10.13.5	Safety and Efficacy
10.13.5.1	Summary of Pivotal Trials
10.13.6	Product Profile
10.14	HEMLIBRA (EMICIZUMAB-KXWH): CHUGAI/ GENENTECH/ROCHE
10.14.1	Product Description
10.14.2	Regulatory Milestones
10.14.3	Other Developmental Activities
10.15	SEVENFACT [COAGULATION FACTOR VIIA (RECOMBINANT)-JNCW]: HEMA BIOLOGICS/LFB PHARMACEUTICALS
10.15.1	Product Description
10.15.2	Regulatory Milestones
10.15.3	Other Developmental Activities
10.15.4	Recent Clinical Development
10.15.4.1	Clinical trials information
10.15.5	Safety and Efficacy
10.15.5.1	Summary of Pivotal Trial
10.15.6	Product Profile
10.16	HEMGENIX (ETRANACOGENE DEZAPARVOVEC): CSL BEHRING/UNIQURE
10.16.1	Product Description
10.16.2	Regulatory Approval
10.16.3	Other Development Activities
10.16.4	Recent Clinical Development
10.16.5	Safety and Efficacy
10.16.6	Product Profile
10.17	REBINYN (NONACOG BETA PEGOL): NOVO NORDISK
10.17.1	Product Description
10.17.2	Regulatory Milestones
10.17.3	Other Developmental Activities
10.17.4	Recent Clinical Development
10.17.4.1	Clinical Trials Information
10.17.5	Safety and Efficacy
10.17.5.1	Summary of Pivotal Trials
10.17.6	Product Profile
10.18	IDELVION: CSL BEHRING
10.18.1	Product Description
10.18.2	Regulatory Milestones
10.18.3	Other Developmental Activities
10.18.4	Safety and efficacy
10.18.4.1	Summary of Pivotal Trial
10.18.5	Product Profile
10.19	ALPROLIX: SANOFI /BIOVERATIV THERAPEUTICS/SOBI
10.19.1	Product Description
10.19.2	Regulatory Milestones
10.19.3	Other Developmental Activities
10.19.4	Safety and Efficacy
10.19.4.1	Summary of Pivotal Trial
10.19.5	Product Profile
10.2	IXINITY (TRENONACOG ALFA): MEDEXUS PHARMACEUTICALS/APTEVO THERAPEUTICS
10.20.1	Product Description
10.20.2	Regulatory Milestones
10.20.3	Other Developmental Activities
10.20.4	Safety and Efficacy
10.20.4.1	Summary of Pivotal Trials
10.20.5	Product Profile
10.21	RIXUBIS: TAKEDA (SHIRE/BAXTER)
10.21.1	Product Description
10.21.2	Regulatory Milestones
10.21.3	Other Developmental Activities
10.21.4	Safety and Efficacy
10.21.4.1	Summary of Pivotal Trial
10.21.5	Product Profile
10.22	VONVENDI: SHIRE
10.22.1	Product Description
10.22.2	Mechanism of Action
10.22.3	Regulatory Milestones
10.22.4	Advantages and Disadvantages
10.22.5	Recent Clinical Development
10.22.5.1	Clinical Trials Information
10.22.6	Safety and Efficacy
10.22.7	Product Profile
10.23	HUMATE-P/HAEMATE P: CSL BEHRING
10.23.1	Product Description
10.23.2	Mechanism of Action
10.23.3	Regulatory Milestones
10.23.4	Advantages and Disadvantages
10.23.5	Safety and Efficacy
10.23.6	Product Profile
10.24	ALPHANATE: GRIFOLS BIOLOGICAL INC.
10.24.1	Product Description
10.24.2	Mechanism of Action
10.24.3	Regulatory Milestones
10.24.4	Advantages and Disadvantages
10.24.5	Safety and Efficacy
10.24.6	Product Profile
10.25	COAGADEX: BIO PRODUCTS LABORATORY
10.25.1	Product Description
10.25.2	Regulatory Milestones
10.25.3	Other Developmental Activities
10.25.4	Pivotal Clinical Trial
10.25.4.1	Summary of Pivotal Clinical Trials
10.25.5	Safety and Efficacy
10.25.6	Product Profile
10.26	ANDEXXA: ALEXION ASTRAZENECA RARE DISEASE
10.26.1	Product Description
10.26.2	Regulatory Milestones
10.26.3	Other Developmental Activities
10.26.4	Pivotal Clinical Trial
1.1.1.2	Summary of Pivotal Clinical Trials
10.26.5	Safety and Efficacy
10.26.6	Product Profile
10.27	KCENTRA: CSL BEHRING
10.27.1	Product Description
10.27.2	Regulatory Milestones
10.27.3	Other Developmental Activities
10.27.4	Ongoing Current Clinical Pipeline Activity
10.27.5	Pivotal Clinical Trial
10.27.5.1	Summary of Pivotal Clinical Trials
10.27.6	Safety and Efficacy
10.27.7	Product Profile
10.28	TRETTEN® (CATRIDECACOG): NOVONORDISK
10.28.1	Product Description
10.28.2	Regulatory Milestones
10.28.3	Pivotal Clinical Trial
10.28.4	Safety and Efficacy
10.28.5	Product Profile
10.29	OCTAPLEX: OCTAPHARMA
10.29.1	Product Description
10.29.2	Regulatory Milestones
10.29.3	Other Developmental Activities
10.29.4	Recent Clinical Development
10.29.5	Pivotal Clinical Trial
10.29.6	Safety and Efficacy
10.29.7	Product Profile
10.3	RIASTAP: CSL BEHRING
10.30.1	Product Description
10.30.2	Regulatory Milestones
10.30.3	Other Developmental Activities
10.30.4	Pivotal Clinical Trial
10.30.5	Safety and Efficacy
10.30.6	Product Profile
10.31	ROCTAVIAN (VALOCTOCOGENE ROXAPARVOVEC): BIOMARIN PHARMACEUTICAL
10.31.1	Product Description
10.31.2	Regulatory Milestone
10.31.3	Other developmental activities
10.31.4	Recent clinical developmental activities
10.31.5	Safety and efficacy
10.31.6	Product Profile
10.32	ALTUVIIIO (EFANESOCTOCOG ALFA) (RFVIIIFC-VWF-XTEN): SANOFI
10.32.1	Product Description
10.32.2	Regulatory Milestone
10.32.3	Other developmental activity
10.32.4	Recent Clinical development
10.32.4.1	Clinical trial information
10.32.5	Safety and efficacy
10.32.6	Product Profile
11	EMERGING DRUGS
11.1	KEY CROSS
11.2	CONCIZUMAB (NN7415): NOVO NORDISK
11.2.1	Product description
11.2.2	Other developmental activities
11.2.3	Clinical development Activities
11.2.3.1	Clinical trial information
11.2.4	Safety and efficacy
11.3	FIDANACOGENE ELAPARVOVEC: PFIZER/SPARK THERAPEUTICS
11.3.1	Product Description
11.3.2	Other Developmental Activities
11.3.3	Clinical Developmental Activities
11.3.3.1	Clinical Trials Information
11.3.4	Safety and Efficacy
11.4	RG6357 (SPK-8011): ROCHE (SPARK THERAPEUTICS)
11.4.1	Product description
11.4.2	Other developmental activity
11.4.3	Clinical development Activities
11.4.3.1	Clinical trial information
11.4.4	Safety and efficacy
11.5	FITUSIRAN (ALN-AT3, SAR-439774): SANOFI (GENZYME)/ALNYLAM PHARMACEUTICALS
11.5.1	Product description
11.5.2	Other developmental activity
11.5.3	Clinical development Activities
11.5.3.1	Clinical trial information
11.5.4	Safety and efficacy
11.6	MARSTACIMAB (PF-06741086): PFIZER
11.6.1	Product description
11.6.2	Other developmental activities
11.6.3	Clinical development Activities
11.6.3.1	Clinical trial information
11.6.4	Safety and efficacy
11.7	GIROCTOCOGENE FITELPARVOVEC (SB-525 OR PF-07055480): PFIZER/SANGAMO THERAPEUTICS
11.7.1	Product description
11.7.2	Other developmental activity
11.7.3	Clinical development Actvities
11.7.3.1	Clinical trial information
11.7.4	Safety and efficacy
11.8	NNC0365-3769 A (MIM8): NOVO NORDISK A/S
11.8.1	Product description
11.8.2	Other developmental activity
11.8.3	Clinical development Activities
11.8.3.1	Clinical trial information
11.8.4	Safety and efficacy
11.9	BT524: BIOTEST AG
11.9.1	Product Description
11.9.2	Other Developmental Activities
11.9.3	Clinical Development Activities
11.9.3.1	Clinical Trials Information
11.9.4	Safety and Efficacy
11.10	SERPINPC: CENTESSA PHARMACEUTICALS (APCINTEX)
11.10.1	Product description
11.10.2	Other developmental activities
11.10.3	Clinical development Activities
11.10.3.1	Clinical trial information
11.10.4	Safety and efficacy
11.11	STSP-0601: STAIDSON BIOPHARMA INC.
11.11.1	Product Description
11.11.2	Clinical Development Activities
11.11.2.1	Clinical Trials Information
11.11.3	Safety and Efficacy
11.12	MARZEPTACOG ALFA: GC BIOPHARMA
11.12.1	Product Description
11.12.2	Other Developmental Activities
11.12.3	Clinical Development Activities
11.12.3.1	Clinical Trials Information
11.12.4	Safety and Efficacy
11.13	AB023: ARONORA, INC.
11.13.1	Product Description
11.13.2	Other Developmental Activities
11.13.3	Clinical Development Activities
11.13.3.1	Clinical Trials Information
11.13.4	Safety and Efficacy
11.14	BAY2599023 (DTX201 AAV FVIII): BAYER/ULTRAGENYX PHARMACEUTICAL
11.14.1	Product description
11.14.2	Other developmental activity
11.14.3	Clinical development Activities
11.14.3.1	Clinical trial information
11.14.4	Safety and efficacy
11.15	OPK88005 (FACTOR VIIA-CTP): OPKO HEALTH, INC.
11.15.1	Product Description
11.15.2	Other Developmental Activities
11.15.3	Clinical Development Activities
11.15.3.1	Clinical Trials Information
11.15.4	Safety and Efficacy
12	COAGULATION FACTOR DEFICIENCY: SEVEN MAJOR MARKET ANALYSIS
12.1	KEY FINDINGS
12.2	MARKET OUTLOOK
12.3	KEY MARKET FORECAST ASSUMPTIONS
12.4	TOTAL MARKET SIZE OF COAGULATION FACTOR DEFICIENCY IN THE 7MM
12.5	UNITED STATES MARKET SIZE
12.5.1	Total Market Size of Coagulation Factor Deficiency in the United States
12.6	EU4 AND THE UK MARKET SIZE
12.6.1	Total Market Size of Coagulation Factor Deficiency in the EU4 and the UK
12.7	JAPAN
12.7.1	Total Market Size of Coagulation Factor Deficiency in Japan
13	MARKET ACCESS AND REIMBURSEMENT
13.1	HEMOPHILIA A
13.1.1	The US
13.1.1.1	Current Therapies
13.1.2	HAS Assessment for Some Other Therapies
13.1.3	HTA Assessment of Hemlibra by NHS and IQWiG
13.1.4	IQWIG Assessment for Some Other Therapies
13.1.5	Future Therapies: Gene Therapy
13.2	HEMOPHILIA B
13.2.1	Access and Reimbursement Overview for Current and Future Therapies
13.2.2	NICE Assessment
13.2.3	IQWIG Assessment
13.2.4	HAS Assessment
13.3	CLOTTING FACTORS
13.3.1	The US
13.3.1.1	CMS
13.3.2	UK (NHS)
13.3.3	EU (HTA Assessment)
13.3.3.1	IQWIG
13.3.3.2	AIFA
13.3.4	Japan
14	UNMET NEEDS
15	SWOT ANALYSIS
16	KOL VIEWS
17	APPENDIX
17.1	BIBLIOGRAPHY
17.2	REPORT METHODOLOGY
18	DELVEINSIGHT CAPABILITIES
19	DISCLAIMER
20	ABOUT DELVEINSIGHT

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