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市場調查報告書
商品編碼
1787906
全球結節性癢疹治療市場分析及預測(至2032年):依治療類型、給藥途徑、診斷方法、結節性癢疹類型、通路及地區分類Prurigo Nodularis Treatment Market Forecasts to 2032 - Global Analysis By Treatment Type, Route of Administration, Diagnosis Method, Type of Nodular Prurigo, Distribution Channel and By Geography |
根據 Stratistics MRC 的數據,全球結節性癢疹治療市場預計在 2025 年將達到 22 億美元,到 2032 年將達到 34 億美元,預測期內的複合年成長率為 6.3%。結節性癢疹的治療著重於緩解劇烈搔癢、縮小結節性病變和改善生活品質。治療通常包括局部治療(例如皮質類固醇和止癢膏)、全身生物製藥(例如度普利尤單抗))和照光治療。皮膚科醫生根據嚴重程度和潛在疾病制定治療計劃。對患者進行避免抓撓和維持正確護膚的教育至關重要。定期後續觀察有助於後續觀察並調整治療方法,以長期控制症狀並促進皮膚癒合。
結節性癢疹的盛行率和診斷率不斷上升
結節性癢疹的盛行率不斷上升,尤其是在患有慢性皮膚病和全身性疾病的人群中,是該疾病的主要成長動力。醫療保健提供者和患者意識的提高,使得診斷能夠更早、更準確。皮膚科診療和治療方法工具的普及也進一步推動了這一趨勢。隨著疾病負擔的加重,對有效治療方法的需求也隨之成長,尤其是那些針對潛在免疫機製而非僅僅治療症狀的治療。
最先進治療價格高昂,新興市場獲得治療的機會有限
儘管生物製藥和標靶治療取得了令人鼓舞的進展,但這些治療方法高成本仍然是一個重大障礙。在開發中地區,有限的報銷框架和不均衡的醫療基礎設施限制了患者獲得治療的機會。此外,醫生培訓和對新治療方法認知的差距也阻礙了新療法的推廣。總而言之,這些挑戰減緩了市場滲透,並限制了創新解決方案的普及。
增加對生物目標和小分子療法的研發投入
製藥公司正致力於開發能夠打破搔癢-抓癢循環並調節免疫反應的生物製藥和小分子藥物。突破性療法認定等監管支持正在加速臨床試驗和核准。產學研之間的策略合作也正在拓展治療藥物研發線。這些努力有望帶來更安全、更有效的治療方法,並拓寬市場基礎。
新療法的限制性報銷政策
儘管像杜匹魯單抗和奈莫利珠單抗這樣的生物製藥表現出了強大的療效,但它們的推廣應用卻受到嚴格的報銷政策的限制,尤其是在北美和西歐以外的地區。由於成本高且長期數據有限,付款方仍持謹慎態度。這種經濟不確定性可能會阻礙生物製劑的廣泛應用並減緩創新。如果醫保覆蓋範圍不擴大,許多患者可能會繼續依賴療效較差的傳統療法。
疫情對結節性癢疹治療市場產生了雙重影響。一方面,供應鏈中斷和皮膚科就診人數減少暫時減緩了治療的普及。另一方面,人們對慢性病的認知提高以及遠距皮膚科的普及促進了遠距會診和護理的連續性。這場危機也加速了數位醫療的普及,使疾病監測和病患參與度得到改善,最終促進了市場的復甦和成長。
預計系統性治療領域將成為預測期內最大的領域
預計系統性治療領域將在預測期內佔據最大市場佔有率,這得益於其在重症和難治性病例中的卓越療效。這些治療方法優於局部用藥,因為它們透過針對發炎途徑提供長期緩解。核准生技藥品的日益普及以及正在進行的新型藥物臨床試驗正在推動該市場的發展。
預計預測期內慢性結節性癢疹的複合年成長率最高。
慢性結節性癢疹預計將在預測期內達到最高成長率。慢性結節性癢疹的特徵是持續性搔癢和抗治療性的結節,需要先進的治療方法。此疾病的致殘性促使患者尋求長期治療方案,從而推動了對生物製藥和免疫調節劑的需求。診斷和認知的提高進一步推動了市場成長。
由於皮膚病患病率上升、醫療基礎設施不斷擴展以及生物製藥可近性的不斷提高,預計亞太地區將在預測期內佔據最大的市場佔有率。中國、印度和日本等國家正在推動皮膚病學現代化,並加大對臨床研究的投資,以提高治療效果。政府為促進皮膚健康和早期診斷的措施也為該地區的主導地位做出了貢獻。
在預測期內,北美預計將呈現最高的複合年成長率,這得益於其先進的醫療基礎設施和生物療法的早期應用。美國在臨床研究方面處於領先地位,目前正在進行大量針對IL-31和IL-4/13抑制劑等新型藥物的臨床試驗,從而重塑治療格局。加拿大雖然在報銷政策方面略顯保守,但正在透過公共衛生計畫和Dupixent等生物製藥的監管核准來擴大其可及性。該地區對慢性病管理和數位皮膚病學平台的關注正在推動市場成長。
According to Stratistics MRC, the Global Prurigo Nodularis Treatment Market is accounted for $2.2 billion in 2025 and is expected to reach $3.4 billion by 2032 growing at a CAGR of 6.3% during the forecast period. Prurigo Nodularis treatment focuses on alleviating intense itching, reducing nodular lesions, and improving quality of life. Management typically involves topical therapies such as corticosteroids and anti-itch creams, systemic medications like immunomodulators or biologics (e.g., dupilumab), and phototherapy. Dermatologists tailor treatment plans based on severity and underlying conditions. Patient education on avoiding scratching and maintaining proper skin care is essential. Regular follow-ups help monitor progress and adjust therapies, aiming for long-term symptom control and skin healing.
Rising prevalence and increased diagnosis rates of prurigo nodularis
The increasing incidence of prurigo nodularis, particularly among individuals with chronic dermatological and systemic conditions, is a major growth driver. Enhanced awareness among healthcare providers and patients has led to earlier and more accurate diagnoses. This trend is further supported by improved access to dermatology consultations and diagnostic tools. As the disease burden grows, so does the demand for effective therapies, especially those targeting the underlying immunological mechanisms rather than just symptomatic relief.
High cost of advanced therapies and limited access in emerging markets
Despite promising developments in biologics and targeted treatments, the high cost of these therapies remains a significant barrier. In developing regions, limited reimbursement frameworks and uneven healthcare infrastructure restrict patient access. Additionally, gaps in physician training and awareness about newer treatment modalities further hinder adoption. These challenges collectively slow market penetration and limit the reach of innovative solutions.
Increasing investment in R&D for targeted biological and small molecule therapies
Pharmaceutical companies are intensifying their focus on developing biologics and small molecule drugs that disrupt the itch-scratch cycle and modulate immune responses. Regulatory support, such as breakthrough therapy designations, is accelerating clinical trials and approvals. Strategic collaborations between industry and academia are also expanding the therapeutic pipeline. These efforts are expected to yield safer, more effective treatments and broaden the market's scope.
Limited reimbursement policies for novel therapies
While biologics like dupilumab and nemolizumab show strong efficacy, their adoption is constrained by restrictive reimbursement policies, especially outside North America and Western Europe. Payers remain cautious due to high costs and limited long-term data. This financial uncertainty discourages widespread use and may slow innovation. Without broader insurance coverage, many patients may continue relying on less effective conventional treatments.
The pandemic had a dual impact on the prurigo nodularis treatment market. On one hand, supply chain disruptions and reduced dermatology visits temporarily slowed treatment uptake. On the other, heightened awareness of chronic conditions and the expansion of teledermatology encouraged remote consultations and continuity of care. The crisis also accelerated digital health adoption, enabling better disease monitoring and patient engagement, which ultimately supported market recovery and growth
The systemic treatments segment is expected to be the largest during the forecast period
The systemic treatments segment is expected to account for the largest market share during the forecast period due to their superior efficacy in managing severe and refractory cases. These treatments offer long-term relief by targeting inflammatory pathways, making them preferable over topical agents. The growing availability of approved biologics and ongoing clinical trials for novel agents are reinforcing this markets leadership boosting its presence.
The chronic nodular prurigo segment is expected to have the highest CAGR during the forecast period
Over the forecast period, the chronic nodular prurigo segment is predicted to witness the highest growth rate. Chronic nodular prurigo, characterized by persistent, treatment-resistant itch and nodules, demands advanced therapeutic approaches. The debilitating nature of the condition drives patients to seek long-term solutions, boosting demand for biologics and immune modulators. Increased diagnosis and awareness are further fueling the growth of the market.
During the forecast period, the Asia Pacific region is expected to hold the largest market share attributed to rising dermatological disease prevalence, expanding healthcare infrastructure, and growing access to biologic therapies. Countries like China, India, and Japan are investing in dermatology modernization and clinical research, enhancing treatment availability. Government initiatives promoting skin health and early diagnosis are also contributing to regional dominance.
Over the forecast period, the North America region is anticipated to exhibit the highest CAGR driven by its advanced healthcare infrastructure and early adoption of biologic therapies. The United States leads in clinical research, with a high volume of ongoing trials for novel agents such as IL-31 and IL-4/13 inhibitors, which are reshaping the therapeutic landscape. Canada, while slightly more conservative in reimbursement policies, is expanding access through public health initiatives and regulatory approvals for biologics like Dupixent. The region's emphasis on chronic disease management and digital dermatology platforms is accelerating market growth.
Key players in the market
Some of the key players in Prurigo Nodularis Treatment Market include AbbVie Inc, Amgen Inc, AstraZeneca, Bayer AG, Dermavant Sciences, Eli Lilly and Company, Galderma, GlaxoSmithKline plc, Incyte Corporation, Johnson & Johnson Services, Inc, Leo Pharma, Merck & Co., Inc, Novartis AG, Pfizer Inc, Regeneron Pharmaceuticals, Inc, Sanofi, Takeda Pharmaceutical Company Limited, Teva Pharmaceutical Industries Ltd, and UCB S.A.
In June 2025, AbbVie revealed its intention to acquire Capstan Therapeutics to bolster its immunology portfolio, marking another strategic move into next-generation therapies. The deal reflects AbbVie's ongoing commitment to expanding its presence in autoimmune and inflammatory diseases.
In May 2025, Regeneron agreed to acquire genetic testing company 23andMe following its bankruptcy filing, securing its personal genome service and health-research assets. The deal set to close in Q3 2025 retains all staff and establishes an independent privacy ombudsman to oversee consumer data protections
In April 2025, Regeneron announced a long-term partnership worth over $3 billion with Fujifilm Diosynth Biotechnologies to nearly double its biologics production capacity at Holly Springs, NC, and expand manufacturing footprint nationwide.
Note: Tables for North America, Europe, APAC, South America, and Middle East & Africa Regions are also represented in the same manner as above.