세계의 악성 복수 시장 : 시장 인사이트, 역학, 시장 예측(-2034년)
Malignant Ascites - Market Insights, Epidemiology, and Market Forecast - 2034
상품코드 : 1468472
리서치사 : DelveInsight
발행일 : 2024년 03월
페이지 정보 : 영문 113 Pages
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한글목차

악성 복수(MA)는 다양한 복부 및 복부 외부의 원발성 신 생물 별 병태입니다. 이환율의 주요 원인이며 많은 어려움과 치료 과제를 초래합니다. 악성 복수는 복강 내에 악성 세포가 존재하는 복막 암종증의 징후입니다. 악성 복수는 암별 복강 내에 액체가 비정상적으로 저장되는 것을 특징으로 하며 몇 가지 명확한 증상을 나타냅니다. 하나의 주요 지표는 뚜렷한 복부의 부종 또는 팽창이며, 종종 복부 증가로 이어집니다. 악성 복수의 병태 생리학은 다 요인입니다. 종양 혈관의 투과성이 항진하고 복막액이 강제적으로 생산 및 방출되는 것이 악성 복수 발생의 주요 요인입니다.

복강 내 액 생산의 원인은 간경변, 울혈성 심부전, 네프로제, 췌장염, 복막염, 원발성 악성 종양, 간 전이 등 다양합니다. 양성 복수와 악성 복수의 감별은 신체 진찰이나 X선 검사만으로는 불가능합니다. 양자의 감별에는 침습적 검사가 필요합니다.

2020년 주요 7개국에서 악성 복수 시장 규모는 19억 9,000만 달러에 달했습니다. 이 시장은 2034년에는 23억 4,000만 달러로 증가할 것으로 예측됩니다. 미국의 악성 복수 시장 규모는 2020년에 약 8억 달러가 되었지만, 2034년에는 11억 4,500만 달러로 확대될 것으로 예측됩니다. 2034년까지 모든 치료법 중 가장 수익이 예상되는 것은 화학요법(6억 5,000만 달러)이며, 가장 수익이 예상되지 않는 것은 이뇨제 병용 요법(2억 4,000만 달러) 입니다.

EU 4개국과 영국에서 악성 복수 시장 규모는 2020년에 약 4억 9,000만 달러가 되었지만, 2034년에는 5억 4,000만 달러로 증가할 것으로 예측됩니다. 일본의 악성 복수 시장 규모는 2020년 6억 9,000만 달러였지만, 2034년에는 6억 5,000만 달러로 감소할 것으로 예측됩니다.

본 보고서는 주요 7개국의 악성 복수 시장에 대해 조사했으며,, 시장 개요와 함께 역학, 환자 동향, 새로운 치료법, 2034년까지 시장 규모 예측, 의료의 미충족 요구 등을 제공합니다.

목차

제1장 중요한 인사이트

제2장 보고서의 소개

제3장 악성 복수의 주요 요약

제4장 악성 복수 시장 개요

제5장 주요 사건

제6장 악성 복수: 질환의 배경과 개요

제7장 역학과 환자 인구

제8장 환자 동향

제9장 가미시 끝난 약제

제10장 신흥 약제

제11장 악성 복수: 시장 분석

제12장 언멧 요구

제13장 SWOT 분석

제14장 KOL의 견해

제15장 시장 접근과 상환

제16장 부록

제17장 DELVEINSIGHT의 기능

제18장 면책사항

제19장 DELVEINSIGHT 정보

BJH
영문 목차

영문목차

Key Highlights:

DelveInsight's " Malignant ascites - Market Insights, Epidemiology, and Market Forecast - 2034" report delivers an in-depth understanding of Malignant ascites, historical and forecasted epidemiology as well as the Malignant ascites market trends in the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan.

The Malignant ascites market report provides current treatment practices, emerging drugs, Malignant ascites market share of the individual therapies, and current and forecasted Malignant ascites market size from 2020 to 2034, segmented by seven major markets. The report also covers current Malignant ascites treatment practices/algorithms and unmet medical needs to curate the best of the opportunities and assess the underlying potential of the market.

Geography Covered:

Study Period: 2020-2034

Malignant ascites Disease Understanding and Treatment Algorithm

Malignant ascites Overview

Malignant ascites (MA) is a pathological condition due to a variety of primary abdominal and extra-abdominal neoplasms. It is a primary cause of morbidity and presents many difficulties and treatment challenges. Malignant ascite is a sign of peritoneal carcinomatosis, the presence of malignant cells in the peritoneal cavity. Tumors causing carcinomatosis are more commonly secondary peritoneal surface malignancies, which include ovarian, colorectal, pancreatic, and uterine; extra-abdominal tumors originating from lymphoma, lung, and breast; and a small number of unknown primary tumors.

Malignant ascites Diagnosis

The causes of intra-abdominal fluid production are many, including cirrhosis, congestive heart failure, nephrosis, pancreatitis, peritonitis, primary malignancy, or hepatic metastases. It is not possible to distinguish benign ascites from malignant ascites by physical exam or radiographic techniques alone. Invasive testing is necessary to differentiate the two types. Abdominal paracentesis with ascitic fluid analyses can diagnose malignant causes of ascite production in most cases, but laparoscopic tissue sampling may be necessary. Recently, several molecular profiling studies aimed at examining the different contents of MA, such as soluble molecules (proteins, DNA, and RNA), extracellular vesicles (EVs), and cells, have provided new insights into the outcome of PDAC (pancreatic ductal adenocarcinoma) patients with MA.

Further details related to diagnosis will be provided in the report...

Malignant ascites Treatment

With only two approved therapies, i.e., OK-432 and KM-CART in Japan, most patients are limited to the best palliative care, which is often inadequate to address these unmet needs. Several treatment modalities can alleviate the symptoms associated with malignant ascites. Because the natural history of ascite formation is poorly understood, these measures and quality of life data are limited, and the efficacy of existing treatments is difficult to assess. Traditional modalities for managing malignant ascites include sodium-restricted diets, diuretic therapy, serial paracentesis, and peritoneovenous shunting.

Further details related to treatment will be provided in the report.....

Malignant ascites Epidemiology

The Malignant ascites epidemiology chapter in the report provides historical as well as forecasted epidemiology segmented by the total incident cases of Malignant ascites associated cancers, total patient pool of malignant ascites in the 7MM market covering the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan from 2020 to 2034.

Malignant ascites Drug Chapters

The drug chapter segment of the Malignant ascites report encloses a detailed analysis of the early-stage (Phase I/II and Phase I), mid-stage (Phase II and Phase II/III), and late-stage (Phase III) pipeline drug. The current key players for emerging drugs and their respective drug candidates include Lindis Biotech (Catumaxomab), Wuhan YZY Biopharma (M701). The drug chapter also helps understand the Malignant ascites clinical trial details, expressive pharmacological action, agreements and collaborations, approval, and patent details, and the latest news and press releases.

Emerging Drugs

Catumaxomab: Lindis Biotech

Catumaxomab is a bispecific trifunctional antibody that binds directly to the tumor cell with one of its binding sites. It activates two essential components of the immune system with the other binding sites: T cells and macrophages (scavenger cells). The antibody recognizes and binds to all EpCAM-positive tumor cells, including critical cancer stem cells and all CD3-positive T cells. The EpCAM marker is present on almost all carcinomas and is, therefore, a promising approach for targeted cancer treatment. As per company pipeline, catumaxomab is in the preregistration stage of development for the treatment of Malignant ascites.

M 701: Wuhan YZY Biopharma

M701 is a new biological Class I drug that targets both EpCAM and CD3 being developed by YBODY Biotech through its independently patented asymmetric bispecific antibody YBODY(R) platform. The drug is mainly used for the treatment of malignant ascites (MA) and malignant pleural effusion (MPE) derived from EpCAM-positive cancer.M701 dual-antibody targets the EpCAM antigen on one end. At the same time, the CD3 antibody on the other end can bridge T cells and activate T cells to kill EpCAM-positive tumor cells. Currently, M701 is in the Phase II stage of development for the treatment of malignant ascites.

Drug Class Insight

Antibody-dependent cell cytotoxicity

Antibody-Dependent Cellular Cytotoxicity (ADCC) is a crucial mechanism of the immune system involving the targeting and destruction of pathogenic cells by effector cells, particularly natural killer (NK) cells. ADCC is a process where specific antibodies bind to pathogens, marking them for destruction by NK cells through the injection of cytotoxic factors, leading to cell lysis. Antibodies recognize and bind to target cells, which are then attacked and destroyed by effector cells like NK cells. This process plays a vital role in immune responses against pathogens and cancer cells.

Malignant ascites Market Outlook

With only two approved therapies, i.e., OK-432 and KM-CART in Japan, most patients are limited to the best palliative care, which is often inadequate to address these unmet needs.. Only few key players are active in the pipeline such as Lindis Biotech and Wuhan YZY Biopharma for the treatment of Malignant ascites.

OK-432 (Picibanil) is a freeze-dried biological product that is prepared from the Su strain of Streptococcus pyogenes (group A) by treatment with benzylpenicillin and heat. OK-432 has been reported to induce various cytokines, activate immunological cells, and thus augment anticancer immunity.

KM-CART is a novel cell-free and concentrated ascites reinfusion therapy. It is modified from a conventional CART approved by the Ministry of Health, Labor and Welfare in Japan. KM-CART is easier to use and can be applied for massive malignant ascites.

Detailed market assessment will be provided in the final report.

Key Findings

Malignant ascites Drugs Uptake

This section focuses on the uptake rate of potential drugs expected to be launched in the market during 2024-2034. The landscape of Malignant ascites treatment has experienced a transformation with the uptake of novel drugs. These innovative therapies are redefining standards of care. Furthermore, the increased uptake of these transformative drugs is a testament to the unwavering dedication of physicians, oncologists and the entire healthcare community in their tireless pursuit of advancing care. This momentous shift in treatment paradigms is a testament to the power of research, collaboration, and human resilience.

Malignant ascites Pipeline Development Activities

The report provides insights into therapeutic candidates in Phase III, Phase II and Phase I. It also analyzes key players involved in developing targeted therapeutics. Companies like Lindis Biotech and Wuhan YZY Biopharma actively engage in late stage research and development efforts for Malignant ascites. The pipeline of Malignant ascites possesses few potential drugs. However, there is a positive outlook for the therapeutics market, with expectations of growth during the forecast period (2024-2034).

Pipeline Development Activities

The report covers information on collaborations, acquisitions and mergers, licensing, and patent details for Malignant ascites emerging therapy.

Market Access and Reimbursement

In the US healthcare system, both Public and Private health insurance coverage are included. Also, Medicare and Medicaid are the largest government-funded programs in the US. The major healthcare programs, including Medicare, Medicaid, the Children's Health Insurance Program (CHIP), and the state and federal health insurance marketplaces, are overseen by the Centers for Medicare & Medicaid Services (CMS). Other than these, Pharmacy Benefit Managers (PBMs), third-party organizations that provide services and educational programs to aid patients are also present.

A zero-dollar copay program is a healthcare initiative designed to eliminate out-of-pocket costs for patients when obtaining specific medical services or prescription medications. Under this program, individuals enrolled in health insurance plans or prescription drug benefit programs can access certain services or medications without having to make any direct financial contributions in the form of copayments. The program is often implemented to improve medication adherence and access to essential healthcare services, particularly for chronic conditions. Pharmaceutical manufacturers or healthcare providers may offer zero-dollar copay programs as a strategy to make necessary treatments more affordable and accessible for patients, ultimately enhancing overall health outcomes and patient satisfaction.

Detailed market access and reimbursement assessment will be provided in the final report.

Scope of the Report:

Malignant ascites Report Insights

Malignant ascites Report Key Strengths

Malignant ascites Report Assessment

FAQs

Reasons to Buy:

Table of Contents

1. KEY INSIGHTS

2. REPORT INTRODUCTION

3. EXECUTIVE SUMMARY OF MALIGNANT ASCITES

4. MALIGNANT ASCITES MARKET OVERVIEW AT A GLANCE

5. KEY EVENTS

6. MALIGNANT ASCITES: DISEASE BACKGROUND AND OVERVIEW

7. EPIDEMIOLOGY AND PATIENT POPULATION

8. PATIENT JOURNEY

9. MARKETED DRUGS

10. EMERGING DRUGS

11. MALIGNANT ASCITES: MARKET ANALYSIS

12. UNMET NEEDS

13. SWOT ANALYSIS

14. KOL VIEWS

15. MARKET ACCESS AND REIMBURSEMENT

16. APPENDIX

17. DELVEINSIGHT CAPABILITIES

18. DISCLAIMER

19. ABOUT DELVEINSIGHT

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