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시장보고서
상품코드
2052035
Pridopidine : 판매 예측 및 시장 규모(2034년)Pridopidine Sales Forecast, and Market Size Analysis - 2034 |
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DelveInsight
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.
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.
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.
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.
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.
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.
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.
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:
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
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.
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
Pridopidine Competitive Intelligence
Pridopidine Regulatory & Commercial Milestones
Pridopidine Clinical Differentiation
Pridopidine Market Report Highlights