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市場調査レポート
商品コード
1316237
潰瘍性大腸炎(UC)治療の世界市場-2023年~2030年Global Ulcerative Colitis Treatment Market - 2023-2030 |
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カスタマイズ可能
適宜更新あり
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潰瘍性大腸炎(UC)治療の世界市場-2023年~2030年 |
出版日: 2023年07月27日
発行: DataM Intelligence
ページ情報: 英文 195 Pages
納期: 即日から翌営業日
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潰瘍性大腸炎(UC)治療の世界市場は、2022年に69億米ドルに達し、2030年には111億米ドルに達し、有利な成長が予測されています。世界の潰瘍性大腸炎(UC)治療市場は、予測期間中(2023~2030年)に6.3%のCAGRを示すと予測されます。
潰瘍性大腸炎(UC)を含む炎症性腸疾患の増加、研究活動の活発化、製品承認数の増加、合併・買収・共同研究・製品導入などの市場開発などが、予測期間における潰瘍性大腸炎(UC)治療の世界市場の成長を促進すると予想される主な要因です。
潰瘍性大腸炎(UC)の治療薬として承認された製品の増加は、予測期間における潰瘍性大腸炎(UC)治療市場の成長を後押しすると予想されます。例えば、2022年3月、製薬会社AbbVieは、1種類以上の腫瘍壊死因子(TNF)遮断薬で効果不十分または不耐容の中等度から極度の活動性の潰瘍性大腸炎(UC)の成人の治療薬として、RINVOQ(upadacitinib)の米国食品医薬品局(FDA)認可を取得しました。
同様に、2021年11月、欧州委員会はJyseleca(filgotinib)について、成人患者における活動性潰瘍性大腸炎(UC)の治療に対する効能・効果の追加を承認しました。
研究活動の活発化は、世界市場に有望な成長機会をもたらしています。例えば、2021年3月、米国の製薬会社Eli Lilly and Companyはカナダで、活動性の潰瘍性大腸炎(UC)の成人患者を対象にLY3471851の有効性と安全性を評価する第II相臨床試験を開始しました。本試験の終了は2024年10月を予定しています。
潰瘍性大腸炎(UC)の新規開発薬の承認には厳しい規制機関が存在することが、予測期間中の世界市場の成長を阻害しています。例えば、潰瘍性大腸炎(UC)治療の承認と商業化を監督する主な規制機関には、米国食品医薬品局(USFDA)と欧州医薬品庁(EUの医薬品評価・監督機関)があります。
COVID-19のパンデミックと世界各国におけるロックダウンにより、あらゆる業種の企業の財務の健全性が影響を受けています。そのため、COVID-19公衆衛生緊急事態の期間中、米国食品医薬品局(FDA)は、スポンサーと研究者を支援し、試験参加者の安全を確保し、適正臨床実施基準(GCP)を遵守し、試験の完全性に対するリスクを最小限に抑えるための一般的な考慮事項を含むガイドラインを発表しました。
ロシア・ウクライナ紛争は、潰瘍性大腸炎(UC)の有病率が低く、この地域の主要な市場プレーヤーが不足していることから、世界の潰瘍性大腸炎(UC)治療市場に中程度の影響を及ぼすと考えられます。
ウクライナの診療所は、ロシア軍からの侵攻に耐え続けているもの、死者数の増加と限られた医療援助に追われています。あらゆる種類の医薬品が不足しています。ここでも基礎資材の輸出入の重要性が、予測期間中の潰瘍性大腸炎(UC)治療の世界市場の成長に若干の影響を与えると予想されます。
The global ulcerative colitis treatment market reached US$ 6.9 billion in 2022 and is projected to witness lucrative growth by reaching up to US$ 11.1 billion by 2030. The global ulcerative colitis treatment market is expected to exhibit a CAGR of 6.3% during the forecast period (2023-2030).
The growing number of inflammatory bowel diseases including ulcerative colitis, increasing research activities, rising number of product approvals, and market developments such as mergers, acquisitions, collaborations, and product introductions are among the primary factors expected to drive the global ulcerative colitis treatment market growth in the forecast period.
The increasing product approvals for the treatment of ulcerative colitis are expected to boost the global ulcerative colitis treatment market growth in the forecast period. For instance, in March 2022, AbbVie, a pharmaceutical corporation obtained United States Food and Drug Administration (FDA) authorization for RINVOQ (upadacitinib) to treat adults with intermediate to extreme active ulcerative colitis (UC) who have had an insufficient response or intolerance to one or more tumor necrosis factor (TNF) blockers.
Likewise, in November 2021, the European Commission authorized an added indication for Jyseleca (filgotinib) to treat active ulcerative colitis in adult patients.
The increasing research activities are presenting the global market with prospective growth opportunities. For instnace, in March 2021, in Canada, Eli Lilly and Company, an American pharmaceutical company, began a phase II clinical investigation to evaluate the effectiveness and safety of LY3471851 in adult individuals with active ulcerative colitis (UC). The study is estimated to be concluded in October 2024.
The presence of stringent regulatory bodies for the approval of newly developed drugs for ulcerative colitis is hampering the global market growth in the forecast period. For instnace, the major regulatory bodies supervising the authorization and commercialization of ulcerative treatment drugs include the United States Food and Drug Administration (USFDA) and the European Medicines Agency, an agency of the European Union in charge of the evaluation and supervision of pharmaceutical products in European Union.
The financial health of companies across all industries has been impacted by the COVID-19 pandemic and lockdown in numerous nations throughout the world. Therefore, for the period of the COVID-19 public health emergency, the U.S. Food and Drug Administration (FDA) issued guidelines that include general considerations to aid sponsors and researchers, ensuring the safety of trial participants, adhering to good clinical practice (GCP), and minimizing risks to trial integrity.
The Russia-Ukraine conflict is thought to hold a moderate influence on the global ulcerative colitis treatment market, as there is a low prevalence of ulcerative colitis and a lack of primary market players in this region.
Though continuing to countenance invasions from Russian armies, Ukrainian clinics are forced by growing numbers of deaths and limited medical aid. There are shortages across all types of medications. Again, the significance of the import and export of fundamental materials are expected to have a slight impact on the global ulcerative colitis treatment market growth in the forecast period.
The global ulcerative colitis treatment market is segmented based on type, drug class, route of administration, distribution channel, and region.
Owing to the increasing positive outcomes from research investigation the immunosuppressant drug class segment is estimated to hold around 39.8% of the global market in the forecast period. For instance, in June AbbVie, a pharmaceutical corporation reported positive top-line outcomes from COMMAND, its Phase 3 maintenance investigation, revealing risankizumab (SKYRIZI, 180 mg or 360 mg subcutaneous [SC]) attained the preliminary endpoint of clinical remission (per Adapted Mayo Score) at week 52, and critical secondary endpoints in adult individuals with intermediate to extreme active ulcerative colitis.
Owing to the increasing marketing applications acceptance and increasing research approval in Europe is estimated to boost the region's growth attaining 28% of the global market share by 2030. For instance, in December 2022, Pfizer Inc., an American multinational pharmaceutical corporation, reported that The European Medicines Agency (EMA) has received the Marketing Authorization Application (MAA) for etrasimod in the patient inhabitants with the conclusion expected in the first half of 2024.
Also, in August 2022, Abivax SA, a French clinical-stage, publicly traded biotechnology corporation concentrated on designing therapies that modulate the immune system for the treatment of chronic inflammatory conditions, viral diseases, and cancer obtained authorization from the central U.S. Institutional Review Board (IRB) for the protocols for the investigations allowing the beginning of registrations with obefazimod (ABX464) in UC in the U.S. A first-patient-in was expected for the end of the third quarter of this year.
The major global players in the ulcerative colitis treatment market include: Abbott Laboratories, Ajinomoto, AstraZeneca Plc., Eli-Lilly, GlaxoSmithKline Plc., Index Pharmaceuticals Holdings AB, Johnson & Johnson, Merck & Co., Pfizer Inc., and Sanofi, among others.
The global ulcerative colitis treatment market report would provide approximately 53 tables, 54 figures, and 195 Pages.
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