시장보고서
상품코드
2052035

Pridopidine : 판매 예측 및 시장 규모(2034년)

Pridopidine Sales Forecast, and Market Size Analysis - 2034

발행일: | 리서치사: 구분자 DelveInsight | 페이지 정보: 영문 30 Pages | 배송안내 : 2-10일 (영업일 기준)

    
    
    




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한글목차
영문목차

Pridopidine의 성장을 이끄는 주요 요인들

1. 헌팅턴병의 질병 변형 효과를 시사하는 임상적 증거

  • Nature Medicine 저널에 게재된 PROOF-HD 임상 3상 시험 결과에 따르면 프리도피딘은 항도파민제(ADM)를 복용하지 않는 헌팅턴병(HD) 환자의 사전 정의된 하위 그룹에서 임상적 진행을 지연시키고, 기능, 인지, 운동, 인지 및 운동 능력을 유지시키는 것으로 나타났습니다. 능력을 유지하는 것으로 나타났습니다.
  • 이 데이터는 헌팅턴병의 여러 영역에서 임상적으로 의미 있는 질병 진행 지연을 보여주면서 우수한 안전성 프로파일을 유지한 최초의 임상 3상 연구 결과입니다.

2. 근위축성 측삭경화증(ALS) 환자를 대상으로 한 임상 3상 시험 프로그램 확장

FDA는 ALS를 대상으로 한 임상 3상 시험(PREVAiLS)의 시작을 승인했습니다. 본 임상시험은 전 세계 약 500명의 환자를 등록하여 2026년 초에 시작될 예정입니다.

PREVAiLS 임상 2상 HEALEY ALS Platform 임상에서 도출된 유망한 하위 그룹 신호, 즉 초기 급속 진행형 ALS에서 질병 진행 지연, 호흡 기능, 구마비 및 언어 기능 개선, 생존 기간 연장을 확인하는 것을 목표로 하고 있습니다.

3. 전략적 상업적 제휴

Prilenia는 유럽 및 특정 국제 시장에서 프리도피딘의 상업화 및 공동 개발을 위해 Ferrer와 제휴 및 라이선스 계약을 체결했습니다. 계약 총액은 선급금, 마일스톤, 로열티를 포함해 약 5억 유로(약 5억 5,000만 달러)에 달합니다.

4. 광범위하고 확립된 안전 데이터베이스

프리도피딘의 임상 개발 프로그램에는 약 1,600명 이상이 참여했으며, 최대 약 7년간의 안전성 데이터가 축적되어 있습니다. 위약 대조 시험과 장기 투여에서 우수한 내약성 프로파일을 보였습니다.

5. 규제 우대조치 및 희귀질환 치료제 지정

프리도피딘은 헌팅턴병(HD) 및 ALS에 대해 미국과 EU에서 희귀의약품으로 지정되어 있으며, 헌팅턴병(HD)에 대해는 FDA로부터 패스트트랙 지정을 받았습니다.

희귀의약품 지정은 시장 독점권 및 개발 인센티브로 이어질 수 있으며, 패스트트랙 지정은 규제 당국과의 빈번한 대화와 데이터가 승인을 지원하는 경우 우선 심사 가능성을 촉진합니다.

Pridopidine의 최근 동향

2025년 10월, Prilenia Therapeutics B.V.와 Ferrer는 HSG HD 임상연구 컨퍼런스에서 Pridopidine의 임상 진행 지연 및 추가 데이터를 개괄하는 5건의 포스터 발표를 발표할 예정이라고 밝혔습니다.

이 보고서는 미국, EU4(독일, 프랑스, 이탈리아, 스페인, 이탈리아, 스페인, 영국, 일본 등 주요 7개국(미국, EU4, 독일, 프랑스, 이탈리아, 스페인, 영국, 일본)의 프리도피딘(Pridopidine) 시장 동향을 조사하여 근위축성 측삭경화증(ALS), 파킨슨병 등 잠재적 적응증에 대한 포괄적인 인사이트를 제공합니다.

이 보고서는 2020년 2034년까지 프리도피딘의 기존 사용 현황, 잠재적 적응증 진입 전망, 시장 성과에 대한 상세한 분석과 함께 프리도피딘의 잠재적 적응증에 대한 상세한 설명을 제공합니다. 프리도피딘(Pridopidine)의 매출 예측, 작용기전(MoA), 용량 및 투여방법, 규제 마일스톤을 포함한 연구개발(R&D), 기타 활동, 미래 시장 평가, SWOT 분석, 애널리스트 견해, 경쟁 상황, 각 적응증별 기타 신흥 치료제 개요, 시장을 시장을 촉진하는 요인에 대해서도 분석하고 있습니다.

자주 묻는 질문

  • Pridopidine이 헌팅턴병 환자에게 미치는 효과는 무엇인가요?
  • 근위축성 측삭경화증(ALS) 관련 임상 시험의 주요 내용은 무엇인가요?
  • Pridopidine의 상업적 제휴 현황은 어떤가요?
  • 프리도피딘의 안전성 데이터는 어떻게 되나요?
  • 프리도피딘의 규제 우대조치는 무엇인가요?
  • Pridopidine의 시장 동향에 대한 보고서는 어떤 내용을 포함하고 있나요?

목차

제1장 리포트 개요

제2장 Pridopidine 개요 : 근위축성측색경화증(ALS) 및 파킨슨병 등의 잠재적 적응증

제3장 Pridopidine : 경쟁 구도(출시 치료제)

제4장 Pridopidine : 경쟁 구도(후기 개발 단계 신규 치료제)

제5장 Pridopidine : 시장 평가

제6장 Pridopidine : SWOT 분석

제7장 애널리스트의 견해

제8장 부록

제9장 DelveInsight의 서비스 내용

제10장 면책사항

제11장 DelveInsight 소개

제12장 리포트 구입 옵션

KSA

Key Factors Driving Pridopidine Growth

1. Clinical Evidence Suggesting Disease-Modifying Effects in Huntington's Disease

  • Results from the Phase III PROOF-HD trial - published in Nature Medicine - showed that pridopidine slowed clinical progression and maintained function, cognition, and motor performance in a predefined subgroup of HD patients who were not taking antidopaminergic medicines (ADMs).
  • These data represent the first Phase III evidence of clinically meaningful slowing of disease progression across multiple domains in HD with a favorable safety profile.

2. Expansion Into Pivotal Phase III Programs in ALS

The US FDA has cleared the start of a pivotal Phase III trial (PREVAiLS) for ALS, enrolling ~500 patients globally, planned to begin in early 2026.

PREVAiLS is designed to confirm encouraging subgroup signals from the Phase II HEALEY ALS Platform trial showing slowing of disease progression, improvement in respiratory function, bulbar and speech measures, and a survival benefit in early, rapidly progressive ALS.

3. Strategic Commercial Partnerships

Prilenia signed a collaboration and license agreement with Ferrer for the commercialization and co-development of pridopidine in Europe and select international markets, with a total deal value of ~€500 million (~US$550 million) including upfront, milestone, and royalty payments.

4. Broad and Established Safety Database

Pridopidine's clinical development program has involved more than ~1,600 people with safety data extending up to ~7 years, showing a favorable tolerability profile in placebo-controlled studies and long-term exposures.

5. Regulatory Incentives and Orphan Designations

Pridopidine holds Orphan Drug designation in both the US and the EU for HD and ALS, and Fast Track designation by the FDA for HD.

Orphan status can lead to market exclusivity and development incentives, while Fast Track facilitates frequent interactions with regulators and potential priority review if data support approval.

Pridopidine Recent Developments

In October 2025, Prilenia Therapeutics B.V. and Ferrer announced the presentation of five posters outlining slowing of clinical progression and additional pridopidine data at the 2025 HSG HD Clinical Research Congress.

"Pridopidine Sales Forecast, and Market Size Analysis - 2034" report provides comprehensive insights of Pridopidine for potential indication like Amyotrophic lateral sclerosis and Parkinson's disease in the 7MM. A detailed picture of Pridopidine's existing usage in anticipated entry and performance in potential indications in the 7MM, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan for the study period 2020 -2034 is provided in this report along with a detailed description of the Pridopidine for potential indications. The Pridopidine market report provides insights about Pridopidine's sales forecast, mechanism of action (MoA), dosage and administration, as well as research and development including regulatory milestones, along with other developmental activities. Further, it also consists of historical and current Pridopidine performance, future market assessments inclusive of the Pridopidine market forecast analysis for potential indications in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in respective indications. It also provides analysis of Pridopidine sales forecasts, along with factors driving its market.

Pridopidine Drug Summary

Pridopidine is an investigational, orally bioavailable small-molecule agonist of the sigma-1 receptor (S1R) developed by Prilenia Therapeutics, primarily targeting Huntington's disease (HD) and amyotrophic lateral sclerosis (ALS) by modulating cellular stress responses at the mitochondria-associated endoplasmic reticulum membrane. It selectively activates S1R to enhance mitochondrial function, reduce endoplasmic reticulum stress, promote protein clearance, upregulate neurotrophic factors like BDNF, restore synaptic plasticity, and inhibit neuroinflammation, with secondary state-dependent effects on dopamine D2 receptors that normalize cortico-striatal signaling without inducing psychosis. In Phase III trials (e.g., PROOF-HD for early manifest HD), it showed safety and trends in motor/cognitive benefits in subgroups despite missing primary endpoints, alongside promising ALS data; administered at 45 mg BID, common side effects include mild gastrointestinal issues and fatigue. The report provides Pridopidine's sales, growth barriers and drivers, post usage and approvals in multiple indications.

Scope of the Pridopidine Market Report

The report provides insights into:

  • A comprehensive product overview including the Pridopidine MoA, description, dosage and administration, research and development activities in potential indication like Amyotrophic lateral sclerosis and Parkinson's disease.
  • Elaborated details on Pridopidine regulatory milestones and other development activities have been provided in Pridopidine market report.
  • The report also highlights Pridopidine's cost estimates and regional variations, reported and estimated sales performance, research and development activities in potential indications across the United States, Europe, and Japan.
  • The Pridopidine market report also covers the patents information, generic entry and impact on cost cut.
  • The Pridopidine market report contains current and forecasted Pridopidine sales for potential indications till 2034.
  • Comprehensive coverage of the late-stage emerging therapies for respective indications.
  • The Pridopidine market report also features the SWOT analysis with analyst views for Pridopidine in potential indications.

Methodology:

The Pridopidine market report is built using data and information sourced primarily from internal databases, primary and secondary research and in-house analysis by DelveInsight's team of industry experts. Information and data from the secondary sources have been obtained from various printable and nonprintable sources like search engines, news websites, global regulatory authorities websites, trade journals, white papers, magazines, books, trade associations, industry associations, industry portals and access to available databases.

Pridopidine Analytical Perspective by DelveInsight

  • In-depth Pridopidine Market Assessment

This Pridopidine sales market forecast report provides a detailed market assessment of Pridopidine for potential indication like Amyotrophic lateral sclerosis and Parkinson's disease in the seven major markets, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan. This segment of the report provides current and forecasted Pridopidine sales data uptil 2034.

  • Pridopidine Clinical Assessment

The Pridopidine market report provides the clinical trials information of Pridopidine for potential indications covering trial interventions, trial conditions, trial status, start and completion dates.

Pridopidine Competitive Landscape

The report provides Insights on competitors and marketed products within the domain, along with a summary of emerging products and their respective launch dates, posing significant competition in the market.

Pridopidine Market Potential & Revenue Forecast

  • Projected market size for the Pridopidine and its key indications
  • Estimated Pridopidine sales potential (Pridopidine peak sales forecasts)
  • Pridopidine Pricing strategies and reimbursement landscape

Pridopidine Competitive Intelligence

  • Number of competing drugs in development (pipeline analysis)
  • Pridopidine Market positioning compared to existing treatments
  • Pridopidine Strengths & weaknesses relative to competitors

Pridopidine Regulatory & Commercial Milestones

  • Pridopidine Key regulatory approvals & expected launch timelines
  • Commercial partnerships, licensing deals, and M&A activity

Pridopidine Clinical Differentiation

  • Pridopidine Efficacy & safety advantages over existing drugs
  • Pridopidine Unique selling points

Pridopidine Market Report Highlights

  • In the coming years, the Pridopidine market scenario is set to change due to strong adoption, increased prescriptions and broader uptake in multiple immunological indications; which would expand the size of the market.
  • The Pridopidine companies are developing therapies that focus on novel approaches to treat/improve the disease condition, assess challenges, and seek opportunities that could influence Pridopidine's dominance.
  • Other emerging products for Amyotrophic lateral sclerosis and Parkinson's disease are expected to give tough market competition to Pridopidine and launch of late-stage emerging therapies in the near future will significantly impact the market.
  • A detailed description of regulatory milestones, and developmental activities, provide the current development scenario of Pridopidine in potential indications.
  • Analyse Pridopidine cost, pricing trends and market positioning to support strategic decision-making in the immunology landscape.
  • Our in-depth analysis of the forecasted Pridopidine sales data uptil 2034 will support the clients in decision-making process regarding their therapeutic portfolio by identifying the overall scenario of Pridopidine in potential indications.

Key Questions:

  • What is the class of therapy, route of administration and mechanism of action of Pridopidine? How strong is Pridopidine's clinical and commercial performance?
  • What is Pridopidine's clinical trial status in each individual indications such as Amyotrophic lateral sclerosis and Parkinson's disease and study completion date?
  • What are the key collaborations, mergers and acquisitions, licensing and other activities related to the Pridopidine Manufacturers?
  • What are the key designations that have been granted to Pridopidine for potential indications? How are they going to impact Pridopidine's penetration in various geographies?
  • What is the current and forecasted Pridopidine market scenario for potential indications? What are the key assumptions behind the forecast?
  • What are the current and forecasted sales of Pridopidine in the seven major countries, including the United States, Europe (Germany, France, Italy, Spain) and the United Kingdom, and Japan?
  • What are the other emerging products available and how are these giving competition to Pridopidine for potential indications?
  • Which are the late-stage emerging therapies under development for the treatment of potential indications?
  • How cost-effective is Pridopidine? What is the duration of therapy and what are the geographical variations in cost per patient?

Table of Contents

1. Report Introduction

2. Pridopidine Overview in potential indication like Amyotrophic lateral sclerosis and Parkinson's disease

  • 2.1. Product Detail
  • 2.2. Pridopidine Clinical Development
    • 2.2.1. Pridopidine Clinical studies
    • 2.2.2. Pridopidine Clinical trials information
    • 2.2.3. Safety and efficacy
  • 2.3. Other Developmental Activities
  • 2.4. Product Profile

3. Pridopidine Competitive Landscape (Marketed Therapies)

4. Competitive Landscape (Late-stage Emerging Pridopidine Therapies)

5. Pridopidine Market Assessment

  • 5.1. Pridopidine Market Outlook in potential indications
  • 5.2. 7MM Analysis
    • 5.2.1. Pridopidine Market Size in the 7MM for potential indications
  • 5.3. Country-wise Market Analysis
    • 5.3.1. Pridopidine Market Size in the United States for potential indications
    • 5.3.2. Pridopidine Market Size in Germany for potential indications
    • 5.3.3. Pridopidine Market Size in France for potential indications
    • 5.3.4. Pridopidine Market Size in Italy for potential indications
    • 5.3.5. Pridopidine Market Size in Spain for potential indications
    • 5.3.6. Pridopidine Market Size in the United Kingdom for potential indications
    • 5.3.7. Pridopidine Market Size in Japan for potential indications

6. Pridopidine SWOT Analysis

7. Analysts' Views

8. Appendix

  • 8.1. Bibliography
  • 8.2. Report Methodology

9. DelveInsight Capabilities

10. Disclaimer

11. About DelveInsight

12. Report Purchase Options

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