米国の多発性骨髄腫市場：薬剤クラス別、疾患タイプ別、流通チャネル別、地域別、機会、予測、2018年～2032年

米国の多発性骨髄腫の市場規模は、予測期間の2025年～2032年のCAGRが5.50％となり、2024年の80億1,000万米ドルから2032年には122億9,000万米ドルに成長すると予測されています。多発性骨髄腫の罹患率の上昇と早期診断により、治療を求める患者層が拡大しています。早期承認のような規制上の優遇措置が研究開発を促進し、新規治療薬の市場参入を速めています。免疫療法、特に抗CD38モノクローナル抗体の採用が急増しており、治療の嗜好が変化しています。

例えば、米国がん協会は、2025年に米国で新たに多発性骨髄腫と診断される患者数は約3万6,110人（男性2万30人、女性1万6,080人）と予測しています。死亡者数は約1万2,030人で、男性6,540人、女性5,490人と予測されています。米国における多発性骨髄腫の生涯開発リスクは1％未満と推定され、男性では約108人に1人、女性では約133人に1人です。このタイプのがんは主に高齢者が罹患し、35歳未満で発症する症例は1％未満です。診断される人の大半は少なくとも65歳以上であり、診断時の平均年齢は69歳です。

当レポートでは、米国の多発性骨髄腫市場について調査し、市場の概要とともに、薬剤クラス別、疾患タイプ別、流通チャネル別、地域別動向、および市場に参入する企業のプロファイルなどを提供しています。

目次

第1章 プロジェクトの範囲と定義

第2章 調査手法

第3章 米国の関税の影響

第4章 エグゼクティブサマリー

第5章 米国の多発性骨髄腫市場の見通し、2018年～2032年

• 市場規模分析と予測
• 市場シェア分析と予測
  • 薬剤クラス別
    • 免疫調節剤
    • プロテアソーム阻害剤
    • 抗CD38モノクローナル抗体
    • アルキル化剤
    • その他
  • 疾患タイプ別
    • 活動性多発性骨髄腫
    • くすぶり型多発性骨髄腫
  • 流通チャネル別
    • 病院薬局
    • 小売薬局とドラッグストア
    • オンライン薬局
  • 地域別
    • 北西部
    • 南部
    • 西部
    • 中西部
  • 企業別市場シェア分析（上位5社およびその他- 金額別、2024年）
• 2024年の市場マップ分析

第6章 需要供給分析

第7章 バリューチェーン分析

第8章 ポーターのファイブフォース分析

第9章 PESTLE分析

第10章 価格分析

第11章 市場力学

• 市場の促進要因
• 市場の課題

第12章 市場動向と発展

第13章 規制枠組みとイノベーション

• 規制当局の承認
• 臨床試験

第14章 特許の情勢

第15章 ケーススタディ

第16章 競合情勢

• 市場リーダートップ5の競合マトリックス
• 参入企業トップ5のSWOT分析
• 市場の主要企業トップ10の情勢
  • Novartis AG
  • Takeda Pharmaceutical Company Limited
  • Amgen, Inc.
  • AbbVie Inc.
  • Teva Pharmaceuticals, Inc.
  • Bristol-Myers Squibb Company
  • Janssen United States Services, LLC
  • Sanofi S.A.
  • Ono Pharmaceutical Co., Ltd.
  • Genentech, Inc.

第17章 戦略的提言

第18章 調査会社について・免責事項

List of Tables

• Table 1. Competition Matrix of Top 5 Market Leaders
• Table 2. Mergers & Acquisitions/ Joint Ventures (If Applicable)
• Table 3. About Us - Regions and Countries Where We Have Executed Client Projects

List of Figures

• Figure 1. United States Multiple Myeloma Market, By Value, In USD Billion, 2018-2032F
• Figure 2. United States Multiple Myeloma Market Share (%), By Drug Class, 2018-2032F
• Figure 3. United States Multiple Myeloma Market Share (%), By Disease Type, 2018-2032F
• Figure 4. United States Multiple Myeloma Market Share (%), By Distribution Channel, 2018-2032F
• Figure 5. United States Multiple Myeloma Market Share (%), By Region, 2018-2032F
• Figure 6. By Drug Class Map-Market Size (USD Billion) & Growth Rate (%), 2024
• Figure 7. By Disease Type Map-Market Size (USD Billion) & Growth Rate (%), 2024
• Figure 8. By Distribution Channel Map-Market Size (USD Billion) & Growth Rate (%), 2024
• Figure 9. By Region Map-Market Size (USD Billion) & Growth Rate (%), 2024

United States multiple myeloma market is projected to witness a CAGR of 5.50% during the forecast period 2025-2032, growing from USD 8.01 billion in 2024 to USD 12.29 billion in 2032. Rising incidence of multiple myeloma and early diagnosis are expanding the treatment-seeking patient base. Regulatory incentives like accelerated approvals are encouraging R&D and speeding market entry of novel therapies. Surging adoption of immunotherapies, especially Anti-CD38 monoclonal antibodies, is reshaping treatment preferences.

For instance, the American Cancer Society projects that in 2025, there will be approximately 36,110 new diagnoses of multiple myeloma in the United States, comprising 20,030 men and 16,080 women. It is anticipated that around 12,030 fatalities will occur, with 6,540 in men and 5,490 in women. The lifetime risk of developing multiple myeloma in the United States is estimated to be less than 1%, translating to about 1 in 108 for men and 1 in 133 for women; however, individual risk may vary based on specific risk factors. This type of cancer predominantly affects older adults, with less than 1% of cases occurring in individuals under 35 years of age. The majority of those diagnosed are at least 65 years old, with the average age at diagnosis being 69.

Rising Incidences of Multiple Myeloma and Expanding Diagnostic Capabilities

The growing incidence of multiple myeloma in the United States is significantly fueling demand for effective therapeutic options. As one of the most common forms of blood cancer, multiple myeloma accounts for roughly 1.8% of all cancer diagnoses in the country. Early diagnosis and disease monitoring have improved owing to advancements in imaging techniques and laboratory diagnostics such as serum protein electrophoresis and free light chain assays. Moreover, awareness campaigns by organizations like the Multiple Myeloma Research Foundation have boosted early detection rates, allowing for the timely initiation of treatment. This has increased the need for targeted and combination therapies to improve patient survival. To meet rising demand, pharmaceutical companies are investing in robust drug pipelines. For instance, in April 2024, Bristol Myers Squibb announced US FDA approval for a subcutaneous version of Abecma, a CAR-T cell therapy, offering faster administration for relapsed or refractory multiple myeloma.

Robust Pipeline and Accelerated Regulatory Approvals Propel Market Growth

The United States multiple myeloma therapeutics landscape is evolving rapidly with continuous pipeline expansion and an increase in expedited drug approvals by the U.S. Food and Drug Administration (FDA). Due to the high unmet clinical need and the progressive nature of the disease, the FDA offers designations like Fast Track, Breakthrough Therapy, and Orphan Drug to promote quicker access to innovative treatments. This favorable regulatory environment has encouraged major players to develop and commercialize novel agents targeting disease-specific pathways, such as BCMA (B-cell maturation antigen). Pharmaceutical giants are also leveraging biologics, cell therapies, and bispecific antibodies to address treatment-resistant cases. In August 2023, the FDA granted accelerated approval to Johnson & Johnson's bispecific antibody Talvey (talquetamab-tgvs), a first-in-class GPRC5D-targeting therapy for relapsed or refractory multiple myeloma. This milestone illustrates how regulatory incentives are reducing development timelines, bolstering investment in R&D, and increasing the number of approved therapies on the U.S. market.

Growing Preference for Targeted Immunotherapies and Monoclonal Antibodies

Segment-specific growth in the U.S. multiple myeloma market is being significantly driven by rising adoption of targeted immunotherapies, particularly Anti-CD38 monoclonal antibodies such as daratumumab and isatuximab. These therapies have demonstrated superior efficacy over conventional treatment regimens by targeting specific antigens on myeloma cells while sparing healthy tissues. Anti-CD38 agents are increasingly used in frontline therapy settings and in combination with other classes like proteasome inhibitors and immunomodulatory drugs. The growing clinician and patient preference for these biologics is fueled by their proven survival benefits, fewer adverse events, and extended duration of response. Additionally, pharma companies are actively investing in next-generation monoclonal antibodies with enhanced tumor cell-killing properties. For example, in September 2024, the US Food and Drug Administration (FDA) granted approval for Sarclisa (isatuximab) to be used in conjunction with bortezomib, lenalidomide, and dexamethasone (VRd) as a primary treatment option for adult patients diagnosed with newly diagnosed multiple myeloma (NDMM) who are ineligible for autologous stem cell transplants (ASCT). Sarclisa represents the first anti-CD38 therapy that, when combined with the standard VRd regimen, has been shown to significantly decrease the risk of disease progression or mortality (by 40%) compared to VRd alone in patients with NDMM who are not eligible for transplants.

Future Market Scenario (2025-2032F)

The United States multiple myeloma market is poised for strong growth in the coming years due to rising disease incidence, increased awareness, and advances in diagnostic and therapeutic technologies. With a rapidly aging population and improved early detection, the patient pool is expected to expand, driving demand for targeted therapies, immunomodulators, and monoclonal antibodies. Innovations such as CAR-T cell therapies and bispecific antibodies are revolutionizing treatment approaches, offering better survival outcomes and improved quality of life. Additionally, the favorable regulatory environment, coupled with strong investments in research and development, is accelerating drug approvals. As pharmaceutical companies focus on the combination of regimens and personalized medicine, the market is expected to witness robust expansion and continuous clinical innovation.

Key Players Landscape and Outlook

The key players in the market are significantly investing in developing multiple myeloma and are utilizing strategies such as mergers, acquisitions, partnerships, and new product launches to improve their services and competitiveness. Such efforts will propel significant growth in the market, allowing large-cap industry players to increase their presence and, therefore, find new opportunities in this market.

For instance, on November 6, 2024, Nanjing Leads Biolabs Co., Ltd. announced that LBL-034, a humanized bispecific T-cell engaging antibody aimed at GPRC5D and CD3 for the treatment of multiple myeloma, has been granted Orphan Drug Designation (ODD) by the U.S. FDA.

Table of Contents

1. Project Scope and Definitions

2. Research Methodology

3. Impact of U.S. Tariffs

4. Executive Summary

5. United States Multiple Myeloma Market Outlook, 2018-2032F

• 5.1. Market Size Analysis & Forecast
  • 5.1.1. By Value
• 5.2. Market Share Analysis & Forecast
  • 5.2.1. By Drug Class
    • 5.2.1.1. Immunomodulators
    • 5.2.1.2. Proteasome Inhibitor
    • 5.2.1.3. Anti-CD38 Monoclonal Antibody
    • 5.2.1.4. Alkylating Agents
    • 5.2.1.5. Others
  • 5.2.2. By Disease Type
    • 5.2.2.1. Active Multiple Myeloma
    • 5.2.2.2. Smoldering Multiple Myeloma
  • 5.2.3. By Distribution Channel
    • 5.2.3.1. Hospital Pharmacies
    • 5.2.3.2. Retail Pharmacies and Drug Stores
    • 5.2.3.3. Online Pharmacies
  • 5.2.4. By Region
    • 5.2.4.1. Northwest
    • 5.2.4.2. South
    • 5.2.4.3. West
    • 5.2.4.4. Midwest
  • 5.2.5. By Company Market Share Analysis (Top 5 Companies and Others - By Value, 2024)
• 5.3. Market Map Analysis, 2024
  • 5.3.1. By Drug Class
  • 5.3.2. By Disease Type
  • 5.3.3. By Distribution Channel
  • 5.3.4. By Region

6. Demand Supply Analysis

7. Value Chain Analysis

8. Porter's Five Forces Analysis

9. PESTLE Analysis

10. Pricing Analysis

11. Market Dynamics

• 11.1. Market Drivers
• 11.2. Market Challenges

12. Market Trends and Developments

13. Regulatory Framework and Innovation

• 13.1. Regulatory Approvals
• 13.2. Clinical Trials

14. Patent Landscape

15. Case Studies

16. Competitive Landscape

• 16.1. Competition Matrix of Top 5 Market Leaders
• 16.2. SWOT Analysis for Top 5 Players
• 16.3. Key Players Landscape for Top 10 Market Players
  • 16.3.1. Novartis AG
    • 16.3.1.1. Company Details
    • 16.3.1.2. Key Management Personnel
    • 16.3.1.3. Products and Services
    • 16.3.1.4. Financials (As Reported)
    • 16.3.1.5. Key Market Focus and Geographical Presence
    • 16.3.1.6. Recent Developments/Collaborations/Partnerships/Mergers and Acquisitions
  • 16.3.2. Takeda Pharmaceutical Company Limited
  • 16.3.3. Amgen, Inc.
  • 16.3.4. AbbVie Inc.
  • 16.3.5. Teva Pharmaceuticals, Inc.
  • 16.3.6. Bristol-Myers Squibb Company
  • 16.3.7. Janssen United States Services, LLC
  • 16.3.8. Sanofi S.A.
  • 16.3.9. Ono Pharmaceutical Co., Ltd.
  • 16.3.10. Genentech, Inc.

Companies mentioned above DO NOT hold any order as per market share and can be changed as per information available during research work.

17. Strategic Recommendations

18. About Us and Disclaimer