시장보고서
상품코드
1865194

스테로이드 불응성 급성 이식편대 숙주병(SR-aGvHD) : 시장 인사이트, 역학, 예측(2034년)

Steroid Refractory Acute Graft-Versus-Host Disease (SR-aGvHD) - Market Insights, Epidemiology, and Market Forecast - 2034

발행일: | 리서치사: DelveInsight | 페이지 정보: 영문 200 Pages | 배송안내 : 2-10일 (영업일 기준)

    
    
    




■ 보고서에 따라 최신 정보로 업데이트하여 보내드립니다. 배송일정은 문의해 주시기 바랍니다.

주요 하이라이트 :

  • 스테로이드 불응성 급성 이식편대 숙주병(SR-aGVHD)은 이식 후 생존율에 대한 주요 장벽이며, 동종 조혈 줄기 세포 이식(HCT) 후 가장 심각한 합병증 중 하나로 자리 잡고 있습니다. 스테로이드 불응성 사례에서는 지속적인 치료 옵션이 제한되어 있으며 예후도 불량합니다.
  • 특히 고령자층과 고위험 혈액 악성 종양 환자에서 동종 HCT 수술의 세계적인 증가에 따라 SR-aGVHD 환자 수는 계속 확대되고 있으며, 보다 효과적이고 표적화된 치료법의 확립이 시급해지고 있습니다.
  • 2024년에는 미국에서만 약 3만 건의 동종이식이 실시되어, 이식편대 숙주병(GvHD)의 임상적 영향의 크기와 강력한 세컨드라인 치료제의 필요성을 부각했습니다.
  • 2019년에 FDA 승인을 받은 Ruxolitinib은 성인 및 소아 환자층에서 SR-aGVHD 치료의 기초가 되고 있으며, JAK-STAT 신호전달 경로가 중요한 치료 표적임을 입증합니다.
  • 최근 승인된 RYONCIL(레메스템셀-L)은 염증을 조절하고 조직 재생을 촉진하도록 설계된 최초의 승인된 간엽계 줄기세포 치료법으로서, 특히 소아의 SR-aGVHD 치료에 있어서 큰 진전을 나타내고 있습니다.
  • SR-aGVHD의 치료 파이프라인은 neihulizumab(ALTB-168), RLS-0071 등의 신규 면역조절제에 의해 확대를 계속하고 있습니다. 이들은 주요 염증 경로를 표적으로 하면서 이식편대 백혈병 효과를 유지함으로써 치료 효과의 향상을 목표로 하고 있습니다.
  • 전반적으로, SR-aGVHD의 치료 환경은 면역학의 진보, 지원 규제 프레임 워크, 이식의 장기적인 성공을 향상시키기위한 정밀의료 및 세포 기반 요법의 추구에 견인되어 의미있는 혁신을 이루고 있습니다.

본 보고서에서는 스테로이드 불응성 급성 이식편대 숙주병(SR-aGvHD) 를 상세하게 조사하여 동종이식의 총 건수, 급성 GvHD의 유병 사례 총계, 중증도별 급성 GvHD 발생 사례, 장기별 급성 GvHD 발생 사례, SR-aGVHD의 총발생 사례, SR-aGVHD의 치료 사례 등의 과거 및 향후 역학 데이터를 제시하고 있습니다. 또한 진단 프로세스, 처방 패턴, 의사의 견해, 시장 접근, 치료 옵션, 시장 전망 동향을 미국, EU 4개국(독일, 프랑스, 이탈리아, 스페인), 영국, 일본의 주요 7개국 시장에 걸쳐 2020-2034년 기간으로 분석했습니다. 또한 기존의 치료실태와 미충족 수요를 종합적으로 평가하여 시장의 잠재력과 새로운 사업 기회를 명확히 하고 있습니다.

자주 묻는 질문

  • 스테로이드 불응성 급성 이식편대 숙주병(SR-aGVHD)의 치료 환경은 어떻게 변화하고 있나요?
  • 2024년 미국에서 동종이식은 얼마나 실시될 예정인가요?
  • Ruxolitinib의 역할은 무엇인가요?
  • RYONCIL(레메스템셀-L)의 특징은 무엇인가요?
  • SR-aGVHD의 치료 파이프라인에는 어떤 신규 면역조절제가 포함되어 있나요?

목차

제1장 중요한 인사이트

제2장 보고서 개요

제3장 시장 개요

  • 치료법별 시장 점유율 실적
  • 치료법별 시장 점유율 예측

제4장 역학·시장 조사 방법

제5장 주요 요약

제6장 주요 사건

제7장 질병의 배경과 개요

  • 각종 유형
  • 원인
  • 병태생리학
  • 증상
  • 리스크 요인
  • 진단
    • 진단 알고리즘
    • 진단 가이드라인
  • 치료 및 관리
    • 치료 알고리즘
    • 치료 가이드라인

제8장 역학과 환자 인구

  • 주요 조사 결과
  • 전제조건과 근거
  • 주요 7개국 동종 이식의 총 건수
  • 주요 7개국 SR-aGvHD의 유병 사례 총계
  • 미국
  • EU 4개국 및 영국
  • 일본
    • 동종이식의 총 건수
    • 급성 GvHD의 유병 사례 총계
    • 중증도별 급성 GvHD 발생 사례
    • 장기별 급성 GvHD 발생 사례
    • SR-aGvHD의 유병 사례 총계
    • SR-aGvHD의 치료 사례

제9장 진료 프로세스

제10장 시판 치료제

  • 경쟁 구도
  • JAKAFI(ruxolitinib) : Incyte
    • 제품 설명
    • 규제 관련 주요 일정
    • 기타 개발 활동
    • 임상 시험 정보
    • 안전성 및 유효성
  • RYONCIL(remestemcel-L-rknd) : Mesoblast

제11장 신흥 치료제

  • 경쟁 구도
  • RLS-0071(pegtarazimod) : ReAlta Life Sciences
    • 제품 설명
    • 기타 개발 활동
    • 임상 시험 정보
    • 안전성 및 유효성
    • 애널리스트의 견해
  • ALTB-168(Neihulizumab) : AltruBio

제12장 SR-aGvHD : 7개국 시장 분석

  • 주요 조사 결과
  • 주요 시장 예측의 전제조건
  • 시장 전망
  • 속성 분석
  • 주요 7개국 SR-aGvHD의 전체 시장 규모
  • 주요 7개국 스테로이드 불응성 급성 이식편대 숙주병(SR-aGvHD) 시장 규모 : 치료법별
  • 시장 규모 : 미국
  • 시장 규모 : EU 4개국 및 영국
  • 시장 규모 : 일본

제13장 KOL의 견해

제14장 미충족 수요(Unmet Needs)

제15장 SWOT 분석

제16장 SR-aGvHD : 시장 접근 및 상환

제17장 부록

제18장 DelveInsight의 서비스 내용

제19장 면책사항

제20장 DelveInsight 정보

KTH 25.11.24

Key Highlights:

  • Steroid-refractory acute graft-versus-host disease (SR-aGVHD) remains a major barrier to post-transplant survival, representing one of the most severe complications following allogeneic hematopoietic cell transplantation (HCT), with limited durable treatment options and poor prognosis in steroid-resistant cases.
  • The global rise in allogeneic HCT procedures, particularly among aging populations and patients with high-risk hematologic malignancies, is expanding the SR-aGVHD patient pool and reinforcing the urgency for more effective, targeted interventions.
  • In 2024, the United States alone recorded approximately 30,000 allogeneic transplant procedures, underscoring the scale of clinical exposure to graft-versus-host disease and the growing need for robust second-line therapies.
  • Ruxolitinib, approved by the FDA in 2019, remains the cornerstone of SR-aGVHD treatment for both adult and pediatric populations, validating the JAK-STAT signaling pathway as a critical therapeutic target.
  • The recent approval of RYONCIL (remestemcel-L) marks a significant advancement, particularly for pediatric SR-aGVHD, as the first approved mesenchymal stem cell therapy designed to modulate inflammation and support tissue regeneration.
  • The pipeline for SR-aGVHD is expanding with novel immune-regulatory agents such as neihulizumab (ALTB-168), RLS-0071, and others, which aim to offer improved efficacy by targeting key inflammatory pathways while preserving graft-versus-leukemia effects.
  • Overall, the SR-aGVHD treatment landscape is undergoing meaningful innovation, driven by advances in immunology, supportive regulatory frameworks, and the pursuit of precision and cell-based therapies to enhance long-term transplant success.

DelveInsight's comprehensive report titled "Steroid Refractory Acute Graft-Versus-Host Disease - Market Insights, Epidemiology, and Market Forecast - 2034" offers a detailed analysis of SR-aGvHD. The report presents historical and projected epidemiological data covering Total Allogenic Transplant Cases, Total Acute GvHD Cases, Acute GvHD cases by grading, Acute GvHD cases by organ involvement, Total Cases of SR-aGvHD, and Total Treated Cases of SR-aGvHD. In addition to epidemiology, the market report encompasses various aspects related to the patient population. These aspects include the diagnosis process, prescription patterns, physician perspectives, market accessibility, treatment options, and prospective developments in the market across seven major markets: the United States, EU4 (Germany, France, Italy, and Spain), the United Kingdom, and Japan, spanning from 2020 to 2034.

The report analyzes the existing treatment practices and unmet medical requirements in SR-aGvHD. It evaluates the market potential and identifies potential business prospects for enhancing therapies or interventions. This valuable information enables stakeholders to make well-informed decisions regarding product development and strategic planning for the market.

Steroid Refractory Acute Graft-Versus-Host Disease Overview

Acute graft-versus-host disease (aGVHD) is a common complication of allogeneic hematopoietic stem cell transplantation (alloHCT) and is a major cause of morbidity and mortality. Systemic steroid therapy is the first-line treatment for aGVHD, although about half of patients will become refractory to treatment. As the number of patients undergoing alloHCT increases, developing safe and effective treatments for aGVHD will become increasingly important, especially for those whose disease becomes refractory to systemic steroid therapy

Steroid Refractory Acute Graft-Versus-Host Disease Diagnosis and Treatment Algorithm

aGVHD is diagnosed clinically after laboratory analysis, imaging, and/or endoscopic examination to exclude potential differential diagnoses. Biopsy may help confirm the diagnosis but lacks sensitivity and specificity. Following diagnosis, aGVHD severity is graded from mild (grade I) to very severe (grade IV). The recommended first-line treatment for aGVHD is systemic steroid therapy; however, many patients become refractory to steroid therapy. SR-aGVHD can be defined as a clear progression after 3-5 days of treatment or no response after 5-7 days of treatment. SR-aGVHD is associated with a high mortality risk.

Ruxolitinib, an oral Janus kinase (JAK) 1/2 inhibitor, has become a cornerstone treatment for SR-AGVHD. It modulates immune cell development, proliferation, and activation to inhibit cytokine signaling and promote T regulatory cells. The FDA approved ruxolitinib for SR-AGVHD in 2019 based on results of the REACH-1 trial, followed by the EMA in 2022, significantly altering the treatment paradigm and establishing its role as the standard second-line treatment. Mesenchymal stem cells (MSCs) are stem cells with a capacity for pluripotent differentiation. They can be obtained from bone marrow, adipose tissue, or umbilical cord and infused intravenously, usually without adverse event. Supportive care remains essential throughout treatment, including antimicrobial prophylaxis, nutritional support, skin care, and management of fluid and electrolyte imbalances. Regular reassessment at Days 7, 14, and 28 is recommended to monitor therapeutic response and guide escalation.

Steroid Refractory Acute Graft-Versus-Host Disease Epidemiology

The epidemiology section of the SR-aGVHD market report offers information on the patient populations, including historical and projected trends for each of the seven major markets. Examining key opinion leader views from physicians or clinical experts can assist in identifying the reasons behind historical and projected trends. The diagnosed patient pool, their trends, and the underlying assumptions are all included in this section of the report.

This section also presents the data with relevant tables and graphs, offering a clear and concise view of the epidem of SR-aGVHD. Additionally, the report discloses the assumptions made during the analysis, ensuring data interpretation and presentation transparency. This epidemiological data is valuable for understanding the disease burden and its impact on the patient population across various regions.

  • In 2024, the United States accounted for ~30,000 total allogenic transplant cases.
  • In 2024, Germany accounted for ~1000 acute GVHD cases.
  • Among Acute GvHD cases by grading, Grade B[II] aGvHD accounts for the highest number of cases.

Steroid Refractory Acute Graft-Versus-Host Disease Market Outlook

The SR-aGVHD therapeutics market is further expected to increase by the major drivers, such as the rising population, technological advancements, and upcoming therapies in the forecast period (2025-2034).

With ongoing research and continued dedication, the future holds hope for even more effective treatments and, ultimately, a cure for this challenging condition. According to DelveInsight, the SR-aGVHD in the 7MM is expected to change significantly during the forecast period 2025-2034.

Steroid Refractory Acute Graft-Versus-Host Disease Drug Chapters

Marketed Steroid Refractory Acute Graft-Versus-Host Disease Drugs

JAKAFI (ruxolitinib): Incyte

JAKAFI is a first-in-class JAK1/JAK2 inhibitor approved by the US FDA for treatment of steroid-refractory acute GVHD in adult and pediatric patients 12 years and older. In May 2024, Incyte Corporation announced that the US Food and Drug Administration approved JAKAFI for the treatment of steroid-refractory acute GVHD in adult and pediatric patients 12 years and older. The approval was based on data from REACH1, an open-label, single-arm, multicenter study of JAKAFI in combination with corticosteroids in patients with steroid-refractory grade II-IV acute GVHD. It was the first therapy to be approved for this indication.

RYONCIL (remestemcel-L-rknd): Mesoblast

RYONCIL is the first and only FDA-approved, allogeneic, off-the-shelf, bone marrow-derived mesenchymal stromal cell therapy indicated for the treatment of pediatric patients aged 2 months and older, including adolescents and teenagers, with SR-aGvHD. It got FDA approval for SR-aGvHD in December 2024.

Emerging Steroid Refractory Acute Graft-Versus-Host Disease Drugs

The SR-aGVHD market is expected to evolve gradually, driven by the limited number of emerging therapies currently in development. Key players such as RLS-0071, ALTB-168, and others, showing commitment to addressing this unmet need, with ongoing efforts to advance novel treatment options for this complex condition.

RLS-0071 (pegtarazimod): ReAlta Life Sciences

RLS-0071 is an investigational peptide therapy developed by ReAlta Life Sciences that leverages a novel dual mechanism of action to rebalance complement activation and neutrophil-driven inflammation specifically through inhibiting myeloperoxidase, neutrophil extracellular traps (NETs), and complement components. The US FDA has granted it both Orphan Drug and Fast Track designations for SR-aGVHD. The Company is currently conducting a Phase II, open label clinical trial of RLS-0071 in hospitalized patients with SR-aGvHD.

ALTB-168 (Neihulizumab): AltruBio

Neihulizumab is an immune checkpoint regulator that targets PSGL-1. It is designed to trigger the depletion of chronically activated T cells. The US FDA has granted it both Orphan Drug and Fast Track designations for SR-aGVHD. Currently, it has completed Phase I trial, and ReAlta is enrolling a Phase II, open-label clinical trial of RLS-0071 in patients with SR-aGVHD

Steroid Refractory Acute Graft-Versus-Host Disease Market Segmentation

DelveInsight's 'Steroid Refractory Acute Graft-Versus-Host Disease - Market Insights, Epidemiology, and Market Forecast - 2034' report provides a detailed outlook of the current and future SR-aGVHD market, segmented within countries, by therapies, and by classes. Further, the market of each region is then segmented by each therapy to provide a detailed view of the current and future market share of all therapies.

Steroid Refractory Acute Graft-Versus-Host Disease Market Size by Countries

The SR-aGVHD market size is assessed separately for various countries, including the United States, EU4 (Germany, France, Italy, and Spain), the UK, and Japan. In 2024, the United States held a significant share of the overall 7MM (Seven Major Markets) SR-aGVHD market. This dominance is projected to persist, especially with the potential early introduction of new products.

Steroid Refractory Acute Graft-Versus-Host Disease Market Size by Therapies

SR-aGVHD Market Size by Therapies is categorized into current and emerging markets for the study period 2020-2034.

Steroid Refractory Acute Graft-Versus-Host Disease Drugs Uptake

This section focuses on the sales uptake of potential SR-aGVHD drugs that have recently been launched or are anticipated to be launched in the SR-aGVHD market between 2020 and 2034. It estimates the market penetration of SR-aGVHD drugs for a given country, examining their impact within and across classes and segments. It also touches upon the financial and regulatory decisions contributing to the probability of success (PoS) of the drugs in the SR-aGVHD.

The emerging SR-aGVHD therapies are analyzed based on various attributes such as safety and efficacy in randomized clinical trials, order of entry and other market dynamics, and the unmet need they fulfill in the SR-aGVHD market.

Steroid Refractory Acute Graft-Versus-Host Disease Market Access and Reimbursement

DelveInsight's 'Steroid Refractory Acute Graft-Versus-Host Disease - Market Insights, Epidemiology, and Market Forecast - 2034' report provides a descriptive overview of the market access and reimbursement scenario of SR-aGVHD.

This section includes a detailed analysis of the country-wise healthcare system for each therapy, enlightening the market access, reimbursement policies, and health technology assessments.

KOL Views

To keep up with current SR-aGVHD market trends and fill gaps in secondary findings, we interview KOLs and SMEs' working in the SR-aGVHD domain. Their opinion helps understand and validate current and emerging therapies and treatment patterns or SR-aGVHD market trends. This will support the clients in potential upcoming novel treatments by identifying the overall scenario of the market and the SR-aGvHD unmet needs.

Steroid Refractory Acute Graft-Versus-Host Disease: KOL Insights

DelveInsight's analysts connected with 50+ KOLs to gather insights; however, interviews were conducted with 15+ KOLs in the 7MM. These KOLs were from organizations, institutes, and hospitals, such as Mercer University, US, University Hospital Tubingen, Germany, University of Barcelona, Barcelona, Spain, ellvitge-Idibell University Hospital, Barcelona, Spain, University of Leeds, Leeds, UK, and University of Occupational and Environmental Health, Japan, among others.

"The norm is basically that you start them on steroids, and if they're progressing within 3 to 4 days, you'd call them refractory. If they don't get better and don't get worse, they're not responding well. Those who progress need to move quickly to something else because they're not going to do well."

"With ruxolitinib, the median time to response is pretty good, so you're hopefully going to see a response within 7 to 14 days. It's not always that early, but the median time is right around there. No matter what, I'm already trying to think about what I am going to be using next to help me try to get this patient's graft-versus-host disease under control."

Competitive Intelligence Analysis

We conduct a Competitive and Market Intelligence analysis of the SR-aGVHD Market, utilizing various Competitive Intelligence tools such as SWOT analysis and Market entry strategies. The inclusion of these analyses is contingent upon data availability, ensuring a comprehensive and well-informed assessment of the market landscape and competitive dynamics.

Steroid Refractory Acute Graft-Versus-Host Disease Pipeline Development Activities

The report offers an analysis of therapeutic candidates in Phase II and III stages and examines companies involved in developing targeted therapeutics for SR-aGVHD. It provides valuable insights into the advancements and progress of potential treatments in clinical development for this condition.

Pipeline Development Activities

The report covers information on collaborations, acquisition and merger, licensing, patent details, and other information for emerging SR-aGVHD therapies.

Steroid Refractory Acute Graft-Versus-Host Disease Report Insights

  • SR-aGVHD Patient Population
  • Therapeutic Approaches
  • SR-aGVHD Pipeline Analysis
  • SR-aGVHD Market Size and Trends
  • SR-aGVHD Market Opportunities
  • Impact of Upcoming Therapies

Steroid Refractory Acute Graft-Versus-Host Disease Report Key Strengths

  • 10 Years Forecast
  • The 7MM Coverage
  • SR-aGVHD Epidemiology Segmentation
  • Key Cross Competition
  • Highly Analyzed SR-aGVHD Market
  • SR-aGVHD Drugs Uptake

Steroid Refractory Acute Graft-Versus-Host Disease Report Assessment

  • SR-aGVHD Current Treatment Practices
  • Unmet Needs
  • SR-aGVHD Pipeline Product Profiles
  • SR-aGVHD Market Attractiveness

Key Questions:

  • How common is steroid refractory acute graft-versus-host disease?
  • What are the key findings of steroid refractory acute graft-versus-host disease epidemiology across the 7MM, and which country will have the highest number of patients during the study period (2020-2034)?
  • What are the currently available treatments for steroid refractory acute graft-versus-host disease?
  • What are the disease risk, burden, and unmet needs of steroid refractory acute graft-versus-host disease?
  • At what CAGR is the steroid refractory acute graft-versus-host disease market and its epidemiology is expected to grow in the 7MM during the forecast period (2025-2034)?
  • How would the unmet needs impact the steroid refractory acute graft-versus-host disease market dynamics and subsequently influence the analysis of the related trends?
  • What would be the forecasted patient pool of steroid refractory acute graft-versus-host disease in the 7MM covering the United States, EU4 (Germany, France, Italy, and Spain), the UK, and Japan?
  • Among EU4 and the UK, which country will have the highest number of patients during the forecast period (2025-2034)?
  • How many companies are currently developing therapies for the treatment of steroid refractory acute graft-versus-host disease?

Reasons to buy:

  • The report will help in developing business strategies by understanding the latest trends and changing treatment dynamics driving the steroid refractory acute graft-versus-host disease Market.
  • Insights on patient burden, evolution in diagnosis, and factors contributing to the change in the epidemiology of the disease during the forecast years.
  • To understand the existing market opportunity in varying geographies and the growth potential over the coming years.
  • Distribution of historical and current patient share based on real-world prescription data along with reported sales of current treatment in the US, EU4 (Germany, France, Italy, and Spain), the United Kingdom, and Japan.
  • Identification of strong upcoming players in the market will help in devising strategies that will help in getting ahead of competitors.
  • Detailed analysis and ranking of class-wise potential current and emerging therapies under the conjoint analysis section to provide visibility around leading classes.
  • Highlights of Access and Reimbursement policies of approved therapies, barriers to accessibility of off-label expensive therapies, and patient assistance programs.
  • To understand the perspective of Key Opinion Leaders around the accessibility, acceptability, and compliance-related challenges of existing treatment to overcome barriers in the future.
  • Detailed insights on the unmet needs of the existing market so that the upcoming players can strengthen their development and launch strategy.

Frequently Asked Questions:

1. What are the treatment goals for steroid refractory acute graft-versus-host disease?

The primary treatment goals for SR-aGVHD are to rapidly control inflammation, prevent further tissue damage, and improve overall survival while minimizing the risk of treatment-related toxicity. Given the high morbidity and mortality associated with SR-aGVHD, particularly in cases involving the gastrointestinal tract, therapies aim to suppress the pathogenic immune response without causing broad immunosuppression that could predispose patients to life-threatening infections. An ideal treatment should selectively modulate or eliminate activated T cells driving the disease, promote tissue repair, and allow tapering of corticosteroids.

2. What are the challenges in managing steroid refractory acute graft-versus-host disease?

Managing SR-aGVHD presents several critical challenges. First, the condition is associated with high mortality especially in patients with severe gastrointestinal involvement yet therapeutic options remain limited and variably effective. The lack of reliable biomarkers to predict steroid resistance or guide treatment decisions early in the disease course complicates timely intervention. Additionally, many second-line therapies, such as JAK inhibitors or experimental agents, can lead to profound immunosuppression, increasing the risk of opportunistic infections, sepsis, and impaired immune reconstitution. Another challenge is the heterogeneity in clinical presentation and organ involvement, which requires tailored treatment strategies rather than a one-size-fits-all approach.

3. What are the key factors driving the growth of the steroid refractory acute graft-versus-host disease?

The growth of the SR-aGVHD treatment landscape is driven by the rising number of allogeneic stem cell transplants, high unmet clinical need, and poor outcomes with corticosteroids. Regulatory incentives and the success of targeted therapies like ruxolitinib have spurred investment and innovation. Advances in immunology, biomarker development, and supportive care have further enabled earlier diagnosis and expanded treatment opportunities, accelerating market expansion.

4. How will the steroid refractory acute graft-versus-host disease Market and Epidemiology Forecast Report benefit the clients?

The SR-aGVHD Market and Epidemiology Forecast Report offers clients critical insights to inform strategic decision-making. By providing detailed, region-specific epidemiological data, the report helps clients quantify the patient population, identify high-burden segments, and assess market potential. It also tracks current and emerging therapies, competitive dynamics, and unmet needs-enabling clients to evaluate opportunities for differentiation, investment, or partnership. Furthermore, the report outlines regulatory trends, pricing considerations, and forecasted market growth, supporting evidence-based planning for clinical development, commercialization, and resource allocation.

Table of Contents

1. Key Insights

2. Report Introduction

3. Market Overview at a Glance

  • 3.1. Market Share (%) Distribution by Therapies in 2024
  • 3.2. Market Share (%) Distribution by Therapies in 2034

4. Epidemiology and Market Methodology

5. Executive Summary

6. Key Events

7. Disease Background and Overview

  • 7.1. Introduction
  • 7.2. Types
  • 7.3. Causes
  • 7.4. Pathophysiology
  • 7.5. Symptoms
  • 7.6. Risk Factor
  • 7.7. Diagnosis
    • 7.7.1. Diagnostic Algorithm
    • 7.7.2. Diagnostic Guidelines
  • 7.8. Treatment and Management
    • 7.8.1. Treatment Algorithm
    • 7.8.2. Treatment Guidelines

8. Epidemiology and Patient Population

  • 8.1. Key Findings
  • 8.2. Assumptions and Rationale: The 7MM
  • 8.3. Total Allogenic Transplant Cases in the 7MM
  • 8.4. Total Cases of SR-aGvHD in the 7MM
  • 8.5. The US
    • 8.5.1. Total Allogenic Transplant Cases
    • 8.5.2. Total Acute GvHD Cases
    • 8.5.3. Acute GvHD cases by Grading
    • 8.5.4. Acute GvHD cases by organ involvement
    • 8.5.5. Total Cases of SR-aGvHD
    • 8.5.6. Treated Cases of SR-aGvHD
  • 8.6. EU4 and the UK
    • 8.6.1. Total Allogenic Transplant Cases
    • 8.6.2. Total Acute GvHD Cases
    • 8.6.3. Acute GvHD cases by Grading
    • 8.6.4. Acute GvHD cases by organ involvement
    • 8.6.5. Total Cases of SR-aGvHD
    • 8.6.6. Treated Cases of SR-aGvHD
  • 8.7. Japan
    • 8.7.1. Total Allogenic Transplant Cases
    • 8.7.2. Total Acute GvHD Cases
    • 8.7.3. Acute GvHD cases by Grading
    • 8.7.4. Acute GvHD cases by organ involvement
    • 8.7.5. Total Cases of SR-aGvHD
    • 8.7.6. Treated Cases of SR-aGvHD

9. Patient Journey

10. Marketed Therapies

  • 10.1. Key Cross Competition
  • 10.2. JAKAFI (ruxolitinib): Incyte
    • 10.2.1. Drug Description
    • 10.2.2. Regulatory Milestones
    • 10.2.3. Other Development Activities
    • 10.2.4. Clinical Trials Information
    • 10.2.5. Safety and Efficacy
  • 10.3. RYONCIL (remestemcel-L-rknd): Mesoblast
    • 10.3.1. Drug Description
    • 10.3.2. Regulatory Milestones
    • 10.3.3. Other Development Activities
    • 10.3.4. Clinical Trials Information
    • 10.3.5. Safety and Efficacy

11. Emerging Therapies

  • 11.1. Key Cross Competition
  • 11.2. RLS-0071 (pegtarazimod): ReAlta Life Sciences
    • 11.2.1. Drug Description
    • 11.2.2. Other Development Activities
    • 11.2.3. Clinical Trials Information
    • 11.2.4. Safety and Efficacy
    • 11.2.5. Analysts' Views
  • 11.3. ALTB-168 (Neihulizumab): AltruBio
    • 11.3.1. Drug Description
    • 11.3.2. Other Development Activities
    • 11.3.3. Clinical Trials Information
    • 11.3.4. Safety and Efficacy
    • 11.3.5. Analysts' Views

12. SR-aGVHD: Seven Major Market Analysis

  • 12.1. Key Findings
  • 12.2. Key Market Forecast Assumptions
    • 12.2.1. Cost Assumptions and Rebates
    • 12.2.2. Pricing Trends
    • 12.2.3. Analogue Assessment
    • 12.2.4. Launch Year and Therapy Uptake
  • 12.3. Market Outlook
  • 12.4. Attribute Analysis
  • 12.5. Total Market Size of SR-aGVHD in the 7MM
  • 12.6. Market Size of SR-aGVHD by Therapies in the 7MM
  • 12.7. The US Market Size
    • 12.7.1. Total Market Size of SR-aGVHD
    • 12.7.2. Market Size of SR-aGVHD by Therapies
  • 12.8. Market Size of SR-aGVHD in the EU4 and the UK
    • 12.8.1. Total Market Size of SR-aGVHD
    • 12.8.2. Market Size of SR-aGVHD by Therapies
  • 12.9. Japan Market Size
    • 12.9.1. Total Market Size of SR-aGVHD
    • 12.9.2. Market Size of SR-aGVHD by Therapies

13. Key Opinion Leaders' Views

14. Unmet Needs

15. SWOT Analysis

16. SR-aGVHD Market Access and Reimbursement

  • 16.1. United States
    • 16.1.1. Centre for Medicare and Medicaid Services (CMS)
  • 16.2. EU4 and the UK
    • 16.2.1. Germany
    • 16.2.2. France
    • 16.2.3. Italy
    • 16.2.4. Spain
    • 16.2.5. United Kingdom
  • 16.3. Japan
    • 16.3.1. MHLW

17. Appendix

  • 17.1. Bibliography
  • 17.2. Abbreviations and Acronyms
  • 17.3. Report Methodology

18. DelveInsight Capabilities

19. Disclaimer

20. About DelveInsight

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