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시장보고서
상품코드
1553386
멘케스병 : 시장 인사이트, 역학 및 시장 예측(-2034년)Menkes Disease- Market Insights, Epidemiology, and Market Forecast- 2034 |
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주요 7개국에서 멘케스병의 총 시장 규모는 2023년 약 790만 달러에 달했습니다. 이 시장은 예측 기간(2024-2034년) 동안 확대될 것으로 예상됩니다. 주요 7개국 시장 규모는 질병에 대한 인식 증가, 진단법 개선, 멘케스병에 대한 새로운 표적 치료제의 출시로 인해 일정한 CAGR로 증가할 것으로 예상됩니다.
2023년 주요 7개국 중 미국이 약 7억 달러로 가장 큰 시장 규모를 차지하고 2034년까지 더욱 확대될 것으로 예상되며, EU 4개국과 영국 중 프랑스가 2023년 27%로 가장 큰 시장 점유율을 차지할 것으로 예상되며, 스페인은 2023년 12%로 가장 낮은 점유율을 차지할 것으로 예상됩니다. 로 최하위를 차지할 것으로 예상됩니다.
멘케스병은 X-연쇄적으로 유전되는 치명적인 소아 신경퇴행성 질환입니다. 구리의 전신 수송을 담당하는 ATP7A 유전자의 돌연변이로 인해 발생하는 X-연쇄 열성 유전 질환입니다. 멩크스 환자의 삶의 질(QoL)은 중증도, 증상 및 결과 증가를 통해 빠르게 악화됩니다. 신생아는 경련 발작, 근긴장 저하, 혈관 비틀림 및 기타 여러 장기의 결함을 보입니다. 또한, 멘케스 환자의 사망률은 매우 높습니다. 신생아가 이런 치명적인 상황에 처한 것을 보는 것은 부모와 가족에게 매우 고통스러운 일입니다. 가족에 대한 종합적인 경제적, 정신적 지원이 절실히 요구됩니다. 현재 진행 중인 상황과 가족 내 발병 가능성에 대해 가족에게 상담을 제공해야 합니다.
진단은 멘케스병에서 가장 어려운 과제입니다. 생화학적 평가와 같은 검사는 환자의 혈청 구리 및 셀룰로플라즈민 농도를 추정하는 데 유용한 수단입니다. 그러나 출생 시 구리 농도가 정상 수치와 겹치는 경우가 있어 오진을 유발할 수 있습니다. 다른 진단 방법으로는 신경 영상 검사, 뇌파 검사 등이 있지만, 이는 의심스러운 증상이 나타난 후에 시행합니다. 유전자 기반 검사 등 높은 정밀도와 정확도를 가진 진단 기술이 요구되고 있습니다.
현재 약물치료가 가능한 멘케스병 환자는 현재 승인된 치료제가 없습니다. 새로운 파이프라인에서 탐색되고 있는 약물은 거의 없는 실정입니다. 그러나 치료 패러다임의 공백 및 유병률 증가를 고려할 때, 새로운 파이프라인에는 충분한 후보물질이 없습니다. 이 미충족 수요를 채우기 위해서는 많은 정확하고 표적화된 치료제가 필요합니다.
이 보고서는 주요 7개국 멘케스병 시장을 조사했으며, 시장 개요와 함께 역학, 환자 동향, 새로운 치료법, 2034년까지 시장 규모 예측, 의료 미충족 수요 등을 제공합니다.
Key Highlights:
DelveInsight's "Menkes Disease- Market Insights, Epidemiology and Market Forecast- 2034" report delivers an in-depth understanding of the Menkes Disease, historical and forecasted epidemiology as well as the Menkes Disease market trends in the United States, EU4 (Germany, Spain, Italy, and France) and the United Kingdom, and Japan.
The Menkes Disease market report provides current treatment practices, emerging drugs, market share of individual therapies, and current and forecasted 7MM Menkes Disease market size from 2020 to 2034. The report also covers current Menkes Disease treatment practices/algorithms and unmet medical needs to curate the best of the opportunities and assesses the underlying potential of the market.
Study Period: 2020-2034
Menkes Disease Overview
Menkes disease is a lethal infantile neurodegenerative disorder with X-linked inheritance. It is an inherited X-linked recessive disorder caused by mutations in the ATP7A gene that is responsible for the transport of copper throughout the body. The quality of life (QoL) of Menkes patients deteriorates rapidly through growing severity, symptoms, and outcomes. The newborn may experience seizures, low muscle tone, twisted blood vessels, and many other defects in organs. Also, the mortality rate of patients with Menkes is very high. Seeing their newborn child in such a deadly situation is very painful for parents and families as well. Overall financial and emotional support to families is highly needed. Counseling the family about the ongoing situation and the possibility of occurrence of disease in the family should be done.
Menkes Disease Diagnosis
The diagnosis is the most formidable challenge in Menkes. Test such as biochemical evaluation is a useful tool to estimate the serum copper and ceruloplasmin levels in the patient, which are generally found lower in affected cases. But the levels of copper at birth may overlap with normal, resulting in misdiagnosis. Other most available diagnosis techniques are Neuroimaging, EEG, and others, which are performed after suspected symptoms appear. Diagnosis techniques with high accuracy and precision, such as gene-based tests, are the need of the hour.
Menkes Disease Treatment
The patients eligible for pharmacological treatment have no approved agents to treat Menkes disease in the present scenario. Few drugs are being explored in the emerging pipeline. However, looking over the abandoned space in the treatment paradigm and increasing prevalence, the emerging pipeline does not have sufficient candidates. Many accurate and targeted treatments are required to fill this unmet gap.
As the market is derived using the patient-based model, the Menkes Disease epidemiology chapter in the report provides historical as well as forecasted epidemiology segmented by, Diagnosed Prevalent Cases of Menkes Disease, in the 7MM covering the United States, EU4 countries (Germany, France, Italy, and Spain) and the United Kingdom, and Japan from 2020 to 2034.
Further details related to country-based variations are provided in the report
The drug chapter segment of the Menkes Disease report encloses a detailed analysis of Menkes Disease marketed drugs and late-stage (Phase-III and Phase-II) pipeline drugs. It also helps to understand the Menkes Disease clinical trial details, expressive pharmacological action, agreements and collaborations, approval and patent details, advantages and disadvantages of each included drug, and the latest news and press releases.
Emerging Drugs
CUTX-101: Cyprium Therapeutics/Sentynl Therapeutics
CUTX-101 is under investigation for the treatment of Menkes disease and related disorders. It has not yet been established as safe and effective for any such treatment by the US FDA or any other regulatory authorities. However, it is available through an Expanded Access Protocol to obtain further safety and efficacy data that may be used to support the approval of the product and subsequent wider accessibility to Menkes disease patients. The drug received designations from the FDA like Breakthrough Therapy, Fast Track, Rare Pediatric Disease and Orphan Drug Designations. Additionally, the European Medicines Agency granted Orphan Drug Designation for CUTX-101. In December 2023, Cyprium completed the transfer of its proprietary rights and assigned its FDA documents pertaining to CUTX-101 Copper Histidinate product candidate for the treatment of Menkes disease, to Sentynl Therapeutics, Inc. A rolling NDA submission to the FDA for CUTX-101 is underway and expected to be completed by Sentynl in 2024.
Drug Class Insights
The current treatment for Menkes disease involves copper supplementation, usually administered through injections or oral medication. This aims to address the copper deficiency characteristic of the condition. Early intervention is critical for optimal outcomes, as treatment effectiveness diminishes with disease progression. While copper therapy can alleviate some symptoms and improve quality of life, it does not fully reverse the neurological damage already incurred. Supportive therapies, such as physical and occupational therapy, may also be employed to manage symptoms and enhance overall well-being.
Disorders of copper homeostasis are currently recognized across the life span. Their recognition and links to human disease have spanned several decades, beginning with the recognition of a degenerative disorder in the offspring of sheep grazing in copper-deficient pastures, through to the description of infants suffering from a progressive neurodegenerative disorder characterized by epileptic seizures, developmental regression, failure to thrive, and an unusual hair quality (giving the condition its distinctive label of kinky hair disease).
Menkes disease development is unpredictable and rapid and often requires medical assistance. Unfortunately, the prognosis of these patients is poor; unless there is access to copper histidine or other copper replacement therapy, survival generally does not exceed 3.5 years. Currently the management of Menkes disease is based on standard of care including off-label copper supplements (copper histidine or copper chloride), antiepileptic drugs, L-threo-dihydroxyphenylserine, and others.
The advancement in therapeutic approaches open the market for new emerging therapies. New therapeutic approaches for Menkes disease are under development CUTX-101, and others.
Until now, CUTX-101 seems to be the most promising candidate in the clinical pipeline of Menkes disease. The market is expected to react positively to CUTX-101, aiding it in solidifying its position as a leading therapy for this indication, as no other therapy has been able to pave its way to approval yet. We believe the expected approval of emerging therapy and awareness regarding early screening of the disease will allow the market to rise at a significant rate.
This section focuses on the rate of uptake of the potential drugs expected to get launched in the market during the study period 2020-2034. For example, for CUTX-101 (Copper Histidinate), we expect the drug uptake to be medium-fast with a probability-adjusted peak share of around 80%, and years to the peak is expected to be 5 years from the year of launch in the US.
Further detailed analysis of emerging therapies drug uptake in the report....
Menkes Disease Pipeline Development Activities
The report provides insights into different therapeutic candidates in Phase III, Phase II, and Phase I stage. It also analyzes key players involved in developing targeted therapeutics.
Pipeline Development Activities
The report covers detailed information on collaborations, acquisitions and mergers, licensing, and patent details for Menkes Disease emerging therapies.
KOL- Views
To keep up with current market trends, we take KOLs and SMEs' opinions working in the domain through primary research to fill the data gaps and validate our secondary research. Industry Experts contacted for insights on Menkes Disease evolving treatment landscape, patient reliance on conventional therapies, patient's therapy switching acceptability, and drug uptake along with challenges related to accessibility, include The Ohio State University College of Medicine, Columbus, Ohio, United States; University of Iowa, Iowa City, Iowa, the US; University Clinic of Marburg, Marburg, Germany; Department of Immunology, Institut Pasteur, France; Department of Pediatrics, Teikyo University School of Medicine, Tokyo, Japan, and others.
Delveinsight's analysts connected with 50+ KOLs to gather insights, however, interviews were conducted with 15+ KOLs in the 7MM. Their opinion helps to understand and validate current and emerging therapies and treatment patterns or Menkes Disease market trends. This will support the clients in potential upcoming novel treatments by identifying the overall scenario of the market and the unmet needs.
Qualitative Analysis
We perform Qualitative and market Intelligence analysis using various approaches, such as SWOT analysis, and Conjoint Analysis. In the SWOT analysis, strengths, weaknesses, opportunities, and threats in terms of disease diagnosis, patient awareness, patient burden, competitive landscape, cost-effectiveness, and geographical accessibility of therapies are provided. These pointers are based on the Analyst's discretion and assessment of the patient burden, cost analysis, and existing and evolving treatment landscape.
Conjoint Analysis is done to analyze multiple approved and emerging therapies based on relevant attributes such as safety, efficacy, frequency of administration, route of administration, and order of entry. Scoring is given based on these parameters to analyze the effectiveness of therapy.
Further, the therapies' safety is evaluated wherein the acceptability, tolerability, and adverse events are majorly observed, and it sets a clear understanding of the side effects posed by the drug in the trials. In addition, the scoring is also based on the route of administration, order of entry and designation, probability of success, and the addressable patient pool for each therapy. According to these parameters, the final weightage score and the ranking of the emerging therapies are decided.
Market Access and Reimbursement
Reimbursement is a crucial point for any drug after its approval. Many drugs or therapies are not properly recognized by the reimbursement body and may fail to get reimbursed or their reimbursement process gets delayed.
The report further provides detailed insights on the country-wise accessibility and reimbursement scenarios, cost-effectiveness scenario of approved therapies, programs making accessibility easier and out-of-pocket costs more affordable, insights on patients insured under federal or state government prescription drug programs, etc.
Market Insights:
Epidemiology Insights:
Current Treatment Scenario, Marketed Drugs, and Emerging Therapies:
Detailed list will be provided in the report.......