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市場調査レポート
商品コード
1553400
老眼 - 市場の洞察、疫学、市場予測:2034年Presbyopia - Market Insight, Epidemiology, and Market Forecast - 2034 |
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カスタマイズ可能
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老眼 - 市場の洞察、疫学、市場予測:2034年 |
出版日: 2024年08月01日
発行: DelveInsight
ページ情報: 英文 88 Pages
納期: 1~3営業日
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主要7ヶ国の老眼治療の市場規模は、2023年に約170億米ドルとなりました。米国は、2023年、主要7ヶ国の中で米国が最も大きく、約80億3,900万米ドルを占め、2034年までにさらに増加すると予想されます。欧州諸国の中で、ドイツは2023年に16億6,600万米ドル近くの市場規模を持ち、最も高い市場規模を持つ一方、スペインは2023年に9億3,800万米ドルで、老眼の市場規模が最も小さくなっています。日本の老眼市場規模は2023年に26億4,200万米ドルとなり、主要7ヶ国市場全体の16%を占めました。
老眼は、近見視力の漸進的な低下を特徴とする一般的な加齢に関連した疾患であり、通常40歳以降に顕著になり、40~60歳の間に進行します。このような近見視力の低下は、自然な加齢過程によるもので、水晶体内のタンパク質の加齢変化により目のレンズの弾力性が失われ、レンズが厚くなり、硬くなり、柔軟性がなくなります。これらの変化は、水晶体が光線を適切に屈折させる能力を損ない、目の焦点を合わせる能力を低下させます。老眼は、初期老眼、機能性老眼、絶対老眼、早期老眼、夜間老眼など、いくつかのタイプに分類することができます。老眼の主な危険因子は加齢ですが、外傷、全身疾患、心血管系疾患、薬剤の副作用などの要因により、老眼の症状が早期に現れることもあります。初期症状としては、長時間近くを見る作業が困難になったり、眼精疲労が生じたりすることが多く、薄暗い場所では悪化することがあります。その他の一般的な症状としては、様々な距離でのピント調節の遅れ、眼不快感、頭痛、眼精疲労、目を細めること、近くでの作業による疲労や眠気、作業距離の増加、読書時の明るい光の必要性、複視などがあります。これらのメカニズムと症状を理解することは、老眼の効果的な管理と治療にとって非常に重要です。
老眼の診断には、眼科医による網膜、筋肉の完全性、屈折、細隙灯評価、視野、視力の評価を含む包括的な眼科検査が必要です。検眼鏡を使って網膜、視床、脈絡膜を検査します。筋肉の完全性は、患者が動くものを追う能力を観察することで評価します。屈折検査では、角膜と水晶体を通して光の波がどの程度曲がるかを調べ、正しいレンズ処方を特定します。細隙灯検査では前眼部の構造を拡大して観察し、視野検査では周辺視野を測定し、視力検査ではさまざまな距離の明瞭度を評価します。一時的に光の感受性を高める瞳孔拡張点眼薬を使用することもあります。これらの評価により、正確な診断と眼球の健康全般が保証されます。
老眼の治療には、患者の職業や職業上のニーズに合わせた様々な選択肢があり、近くのものに焦点を合わせる目の能力の低下を補うことを目的としています。光学的な矯正は、矯正眼鏡(メガネレンズ)やコンタクトレンズによって達成することができ、より永続的な解決策を求める人には、屈折矯正手術や水晶体移植が実行可能な選択肢となります。屈折矯正手術には、伝導性角膜形成術、レーシック、ラセック、光屈折矯正術などがあり、技術の進歩により、より安全で効果的になってきています。加えて、現在の臨床管理では、非ステロイド性抗炎症薬(NSAIDs)、副交感神経作動薬、ミオティック剤、および他の緩和剤の適応外使用が行われることがあります。これらの治療でよく使用される薬剤には、ピロカルピン、カルバコール、アセクリジン、ブリモニジン、ネパフェナックなどがあります。それぞれの治療オプションは、患者の特定のニーズと状態に基づいて検討され、老眼を管理するための包括的なアプローチを提供します。
当レポートでは、主要7ヶ国における老眼市場について調査し、市場の概要とともに、疫学、患者動向、新たな治療法、2034年までの市場規模予測、および医療のアンメットニーズなどを提供しています。
DelveInsight's "Presbyopia- Market Insights, Epidemiology, and Market Forecast - 2034" report delivers an in-depth understanding of presbyopia, historical and forecasted epidemiology as well as the presbyopia market trends in the United States, EU4, and the UK (Germany, France, Italy, Spain) and the United Kingdom, and Japan.
The presbyopia market report provides current treatment practices, emerging drugs, market share of individual therapies, and current and forecasted 7MM presbyopia market size from 2020 to 2034. The Report also covers current presbyopia treatment practices, market drivers, market barriers, SWOT analysis, reimbursement and market access, and unmet medical needs to curate the best of the opportunities and assess the underlying potential of the market.
Study Period: 2020-2034
Presbyopia Overview
Presbyopia is a common age-related condition characterized by a gradual loss of near-focusing ability, typically becoming noticeable after age 40 and progressing between the ages of 40 and 60. This decline in near vision results from the natural aging process, where the lenses of the eyes lose elasticity due to age-related changes in the proteins within the lens, causing it to thicken, harden, and become less flexible. These changes impair the lens's ability to refract light rays properly, diminishing the eye's focusing capacity. Presbyopia can be categorized into several types, including incipient, functional, absolute, premature, and nocturnal presbyopia. While aging is the primary risk factor for presbyopia, the condition can also manifest prematurely due to factors such as trauma, systemic diseases, cardiovascular conditions, or drug side effects. Early symptoms often include difficulty with prolonged close-up tasks and eye strain, which may worsen in dim light. Other common symptoms encompass delays in focusing at various distances, ocular discomfort, headaches, asthenopia, squinting, fatigue or drowsiness from near work, increased working distance, a need for brighter light when reading, and diplopia. Understanding these mechanisms and symptoms is crucial for the effective management and treatment of presbyopia.
Presbyopia Diagnosis
Diagnosing presbyopia involves a comprehensive eye examination by an ophthalmologist, including assessments of the retina, muscle integrity, refraction, slit-lamp evaluation, visual field, and visual acuity. An ophthalmoscope is used to examine the retina, optic disk, and choroid. Muscle integrity is assessed by observing the patient's ability to follow a moving object. Refractive tests determine how well light waves bend through the cornea and lens to identify the correct lens prescription. A slit-lamp exam provides a magnified view of the eye's anterior structures, while visual field tests measure peripheral vision, and visual acuity tests assess clarity at various distances. Pupil-dilating eye drops may be used, temporarily increasing light sensitivity. These evaluations ensure accurate diagnosis and overall ocular health.
Further details related to diagnosis are provided in the report...
Presbyopia Treatment
Treatment of presbyopia involves various options tailored to the patient's vocational and avocational needs, aiming to compensate for the eye's reduced ability to focus on nearby objects. Optical correction can be achieved through corrective eyeglasses (spectacle lenses) or contact lenses, and for those seeking more permanent solutions, refractive surgery or lens implants are viable options. Refractive surgical procedures include techniques such as Conductive Keratoplasty, LASIK, LASEK, and Photorefractive Keratectomy, which have become safer and more effective with advancements in technology. Additionally, current clinical management may involve off-label use of nonsteroidal anti-inflammatory drugs (NSAIDs), parasympathetic agonists, miotic agents, and other tempering agents. Commonly used agents in these treatments include Pilocarpine, Carbachol, Aceclidine, Brimonidine, and Nepafenac. Each treatment option is considered based on the specific needs and conditions of the patient, providing a comprehensive approach to managing presbyopia.
Presbyopia affects a significant segment of the aging population, yet existing treatments often fall short in terms of cost and accessibility. Advanced surgical options are prohibitively expensive and typically not covered by insurance, creating a barrier for many individuals. There is an urgent demand for affordable, non-invasive solutions that cater to diverse socioeconomic backgrounds.
While topical agents like pilocarpine drops, including the pioneering VUITY, represent a step forward, they have not fully met expectations. The daily cost of approximately USD 3 for a 30-day supply, coupled with a lack of insurance coverage, renders them impractical for many. Real-world feedback and AbbVie's reduction in marketing efforts underscore the need for more effective treatments with fewer applications and longer-lasting effects. Addressing these gaps is crucial for enhancing the quality of life for those affected by presbyopia.
Further details related to treatment are provided in the report...
As the market is derived using a patient-based model, the Presbyopia epidemiology chapter in the report provides historical as well as forecasted epidemiology segmented by, Total Prevalent Cases of Presbyopia, Total Diagnosed Prevalent Cases of Presbyopia, Age-specific Diagnosed Prevalent Cases of Presbyopia, Gender-specific Diagnosed Prevalent Cases of Presbyopia, and Severity-specific Diagnosed Prevalent Cases of Presbyopia, in the 7MM covering, the United States, EU4 countries (Germany, France, Italy, and Spain), United Kingdom, and Japan from 2020 to 2034.
The drug chapter segment of the Presbyopia report encloses a detailed analysis of Presbyopia off-label drugs and late-stage (Phase-III and Phase-II) pipeline drugs. It also helps to understand the Presbyopia 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.
Marketed Drugs
VUITY (pilocarpine HCI ophthalmic solution) 1.25%: Allergan/AbbVie
VUITY (pilocarpine HCI ophthalmic solution) 1.25%, developed by Allergan, is a novel treatment for presbyopia approved by the US FDA In October 2021. This prescription eye drop works by contracting the pupil to enhance near and intermediate vision without significantly affecting distance vision. By leveraging the miotic properties of pilocarpine, VUITY improves focus for close-up tasks, offering a non-invasive alternative to reading glasses. Its approval marks a significant advancement in presbyopia management, providing patients with a convenient and effective option to alleviate the condition's symptoms.
Approved but not launched yet:
QLOSI (pilocarpine hydrochloride ophthalmic solution) 0.4%: Orasis Pharmaceuticals
QLOSI (pilocarpine hydrochloride ophthalmic solution) 0.4%, developed by Orasis Pharmaceuticals, is a novel treatment for presbyopia that was approved by the US FDA in October 2023. This formulation aims to improve near vision by using pilocarpine, a cholinergic muscarinic agonist, to enhance the eye's accommodative ability. The market launch of QLOSI is anticipated in the second half of 2024, offering a new option for patients seeking a non-surgical approach to managing age-related vision decline.
Emerging Drugs
Brimochol PF (VT-1011): Visus Therapeutics
Brimochol PF (VT-1011), which is being developed by Visus Therapeutics, is a novel treatment for presbyopia. This investigational eye drop formulation combines brimonidine, a selective alpha-2 adrenergic agonist, with carbachol, a muscarinic agonist, to improve near vision by enhancing the eye's accommodative response. Currently, Brimochol PF is in the late stages of clinical development, having completed Phase III trials, which have demonstrated its efficacy and safety profile. The product is expected to have its New Drug Application (NDA) filed in the second half of 2024, aiming to offer a new therapeutic option for managing presbyopia.
LNZ100 - 1.75% Aceclidine: LENZ Therapeutics, Inc.
LNZ100 - 1.75% Aceclidine, developed by LENZ Therapeutics, Inc., is a promising treatment for presbyopia. This formulation utilizes Aceclidine, a parasympathomimetic agent, to improve near vision by enhancing the eye's accommodative response. Currently, LNZ100 is in advanced clinical stages, with the company planning to submit an NDA to the FDA in mid-2024. The projected market launch for LNZ100 is targeted for the second half of 2025, positioning it as a key therapeutic option for managing presbyopia.
The market for presbyopia treatments encompasses a diverse range of options, catering to various patient preferences and needs. Non-invasive solutions, such as reading glasses, bifocals, and progressive lenses, offer clear vision at different distances, making them popular among those seeking convenience. Contact lenses, including multifocal and monovision types, further enhance flexibility and field of vision compared to traditional eyewear.
Pharmacological treatments have emerged as promising options. Eye drops like pilocarpine hydrochloride temporarily enhance near vision by constricting the pupil, thus improving depth of field. Among the notable advancements, FDA-approved treatments such as VUITY and QLOSI represent significant progress.
Despite these advancements, the market for presbyopia treatments is still evolving. The current FDA-approved therapies are limited, highlighting a significant gap in available treatment options. This gap presents opportunities for further innovation and development in the field, as there remains a substantial demand for new, effective solutions to address the diverse needs of individuals with presbyopia.
In the upcoming treatment landscape, there are a plethora of companies investigating agents for use in presbyopia which includes Visus Therapeutics and others. There are many more pharma companies which are conducting clinical trials for therapies for presbyopia.
This section focuses on the uptake rate of potential drugs expected to launch in the market during 2020-2034. For example, LNZ100 (Aceclidine) in the US is expected to be launched by 2025 with a peak share of 2%. Aceclidine is anticipated to take 7 years to peak with a medium uptake.
Further detailed analysis of emerging therapies drug uptake in the report...
Presbyopia Pipeline Development Activities
The report provides insights into different therapeutic candidates in Phase III, Phase II, and Phase I. It also analyzes key players involved in developing targeted therapeutics.
Pipeline Development Activities
The report covers information on collaborations, acquisitions and mergers, licensing, and patent details for Presbyopia 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 the secondary research. Industry Experts were contacted for insights on Presbyopia evolving treatment landscape, patient reliance on conventional therapies, patient therapy switching acceptability, and drug uptake along with challenges related to accessibility, including KOL from The Midwest Center for Sight, Des Plaines; University of California, San Francisco; Department of Ophthalmology, Universitatsmedizin, Mannheim; Department of Ophthalmology, University Hospital Morvan; Studi Medici Renna, Melendugno Lecce, Italy; Universidad Miguel Hernandez, Spain; Department of Ophthalmology, Kyorin University School of Medicine, Tokyo; 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 understand and validate current and emerging therapies, treatment patterns, or Presbyopia 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 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 analyzes 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
The high cost of therapies for the treatment is a major factor restraining the growth of the global drug market. Because of the high cost, the economic burden is increasing, leading the patient to escape from proper treatment.
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
The presbyopia Epidemiology and Market Insight report for the 7MM covers the forecast period from 2024 to 2034, providing a projection of market dynamics and trends during this timeframe.
The presbyopia market is quite robust. The major layers are Visus Therapeutics, LENZ Therapeutics, Inc., Glaukos Corporation, and others which are currently developing drugs for the treatment of presbyopia.
The market size is estimated through data analysis, statistical modeling, and expert opinions. It may consider factors such as incident cases, treatment costs, revenue generated, and market trends.
The increase in diagnosed prevalent cases of presbyopia and the launch of emerging therapies are attributed to be the key drivers for increasing the presbyopia market.
Introducing new therapies, advancements in diagnostic techniques, and innovations in treatment approaches can significantly impact the presbyopia treatment market. Market forecast reports may provide analysis and predictions regarding the potential impact of these developments.
The market forecast report may include information on the competitive landscape, profiling key market players, their product offerings, partnerships, and strategies, and helping stakeholders understand the competitive dynamics of the presbyopia market.
3.1.. Market Share (%) Distribution of Presbyopia by Therapies in 2020
3.2.. Market Share (%) Distribution of Presbyopia by Therapies in 2034
7.1.. Introduction
7.3.. Difference between Presbyopia and Hyperopia
7.4.. Risk Factors and Causes of Presbyopia
7.5.. Pathophysiology of Presbyopia
7.6.. Complications of Presbyopia
7.7.. Diagnosis of Presbyopia
7.7.1.. Patient History
7.7.2.. Ocular Examination
7.7.3.. Supplemental Testing
7.7.4.. Eye health evaluation
7.7.5.. Recommended eye examination frequency for pediatric patients and adults
7.7.. Early Detection and Prevention of Presbyopia
7.8.. Current Treatment Practices: Presbyopia
7.8.1.. Treatment Algorithm of Presbyopia
7.8.2.. Optical Correction with Spectacle Lenses
7.8.3.. Optical Correction with Contact Lenses
7.8.4.. Surgical options
7.8.5.. Corneal inlay
7.8.6.. Lens implants
7.8.7.. Treatment Algorithm
7.8.1.. Management Strategies for Correction of Presbyopia- American Optometric Association
7.8.2.. NICE guidance for corneal inlay implantation for correction of presbyopia
7.8.3.. Management guidelines by the American Academy of Ophthalmology
7.8.4.. Analysis of Guidelines
8.1.. Key Findings
8.3.. Assumptions and Rationale: 7MM
8.4.. Total Diagnosed Prevalent Cases of Presbyopia in the 7MM
To be continued in the report