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Sanofi/Regeneron Pharmaceuticals' DUPIXENT Approval Marks a Significant Shift in Chronic Obstructive Pulmonary Disease Treatment Landscape | DelveInsight

Sanofi/Regeneron Pharmaceuticals' DUPIXENT Approval Marks a Significant Shift in Chronic Obstructive Pulmonary Disease Treatment Landscape | DelveInsight

賽諾菲安萬特/再生元製藥公司的DUPIXENt批准標誌着慢性阻塞性肺疾病治療格局的重大轉變 | DelveInsight
PR Newswire ·  11/13 06:31

After over a decade without notable progress in treating chronic obstructive pulmonary disease, patients with this ongoing condition now have two new treatment options, with more expected in the future. Regeneron and Sanofi recently revealed that the FDA has expanded the approved uses of their widely successful drug DUPIXENT to include COPD treatment. This marks the drug's sixth approved indication in the US, following its first approval seven years ago for atopic dermatitis.

長達十年多的時間裏,患有慢性阻塞性肺病的患者一直沒有明顯的治療進展,但如今這種持續的病症患者現在有了兩個新的治療選擇,未來還有更多的選擇。再生元製藥公司和賽諾菲安萬特最近宣佈,FDA已擴大了他們的廣受好評藥物DUPIXENt的批准使用範圍,包括COPD治療。這標誌着該藥物在美國獲得的第六個批准適應症,七年前首次獲得批准用於特應性皮炎治療。

LAS VEGAS, Nov. 12, 2024 /PRNewswire/ -- Chronic obstructive pulmonary disease (COPD) is a progressive lung condition characterized by obstructed airflow, making breathing difficult. It primarily encompasses two main conditions: chronic bronchitis and emphysema, often coexisting. COPD typically develops due to long-term exposure to irritants such as cigarette smoke, air pollution, or occupational dust.

拉斯維加斯,2024年11月12日/美通社/ - 慢性阻塞性肺病(COPD)是一種以氣流受阻爲特徵的進行性肺部疾病,使呼吸困難。主要包括兩種主要症狀:慢性支氣管炎和肺氣腫,通常是共存的。COPD通常是由長期暴露於刺激物,如香菸煙霧、空氣污染或職業性粉塵引起的。

As per DelveInsight analysis, the diagnosed prevalent population of COPD in the 7MM was around 44 million in 2023. These cases of COPD in the 7MM are expected to increase at a significant CAGR of 1.4% throughout the study period (2020–2034).

根據DelveInsight的分析,2023年7Mm的COPD確診患病人口大約爲4400萬。預計在研究時段(2020年至2034年)內,這些7Mm的COPD病例將以1.4%的顯著複合年增長率增加。

As per the estimates, the majority of cases of COPD are in females as compared to males, in the US. But in EU4 and the UK, and Japan the diagnosed cases of males represent the majority of the cases. Overall, in the 7MM, females are predominantly high in number.

根據估計,與男性相比,美國的COPD病例中大多數是女性。但在歐盟4、英國和日本,男性的確診病例佔多數。總體而言,在7Mm地區,女性人數明顯較多。

In 2023, the US had around 3 million, 9 million, 5 million, and 1 million cases of GOLD 1, GOLD 2, GOLD 3, and GOLD 4, respectively based on the severity of airflow limitation. Estimates suggest that airflow limitation was higher in GOLD 2 severity.

根據嚴重度分類,2023年美國的GOLD 1、GOLD 2、GOLD 3和GOLD 4分別有約300萬、900萬、500萬和100萬病例,估計GOLD 2嚴重程度氣流限制更嚴重。

Various types of medications are used to manage COPD symptoms and complications, including bronchodilators, which help relax the muscles around the airways. This relaxation opens the airways and makes breathing easier. Most bronchodilators are administered via an inhaler. In more severe cases, the inhaler may also contain steroids to reduce inflammation.

用於管理COPD症狀和併發症的藥物種類繁多,包括支氣管擴張劑,有助於放鬆氣道周圍的肌肉。這種放鬆打開了氣道,使呼吸更容易。大多數支氣管擴張劑都是通過吸入器給藥。在更嚴重的情況下,吸入器中可能還含有類固醇來減輕炎症。

Some commonly used short-acting and long-acting bronchodilators for COPD management include Albuterol (ProAir HFA, Ventolin HFA, and others), Ipratropium (Atrovent HFA), Levalbuterol (Xopenex), Aclidinium (Tudorza Pressair), Arformoterol (Brovana), and Formoterol (Perforomist).

用於COPD管理的一些常用的短效和長效支氣管擴張劑包括阿爾布特羅爾(ProAir HFA、Ventolin HFA等)、異丙託溴銨(Atrovent HFA)、左布托羅爾(Xopenex)、阿克利丁(Tudorza Pressair)、阿福莫特羅爾(Brovana)和福莫特羅爾(Perforomist)。

In the LABA category, medications such as Striverdi Respimat, Arcapta/Onbrez, Serevent, and Brovana are included, while the LAMA class features drugs like Spiriva (available as Spiriva HandiHaler and Spiriva Respimat), Tudorza Pressair, Incruse Ellipta, Yupelri, Seebri Neohaler, and Lonhala Magnair. Since the generic version of Brovana was approved in April 2020, its market share has declined. Additionally, Arcapta Neohaler, Seebri Neohaler, and Utibron Neohaler were discontinued in the US in March 2020, which means they no longer contribute to market size.

在LABA類別中,包括Striverdi Respimat、Arcapta/Onbrez、Serevent和Brovana在內,而LAMA類別則包括Spiriva(可作爲Spiriva HandiHaler和Spiriva Respimat提供)、Tudorza Pressair、Incruse Ellipta、Yupelri、Seebri Neohaler和Lonhala Magnair等藥物。自2020年4月批准Brovana的仿製藥以來,其市場份額已經下降。此外,Arcapta Neohaler、Seebri Neohaler和Utibron Neohaler已於2020年3月在美國停產,這意味着它們不再對市場規模有貢獻。

Patients who do not respond to single therapies are often prescribed double or triple therapy. Among the double therapies, the LABA+ICS combination is widely recommended, with drugs such as Symbicort, Breo Ellipta, and Advair. There are also LABA+LAMA combinations, including Anoro Ellipta, Stiolto Respimat, and Bevespi Aerosphere.

不對單一療法產生反應的患者常常會被開具雙重或三重療法。在雙重療法中,LABA+ICS組合被廣泛推薦,其中包括Symbicort、Breo Ellipta和Advair等藥物。還有LABA+LAMA組合,包括Anoro Ellipta、Stiolto Respimat和Bevespi Aerosphere等。

In July 2020, the US FDA approved AstraZeneca's BREZTRI AEROSPHERE for the maintenance treatment of patients with COPD. Additionally, in October 2020, TRIXEO AEROSPHERE (a combination of formoterol fumarate, glycopyrronium bromide, and budesonide) received marketing authorization in the EU for the maintenance treatment of adult patients with moderate to severe COPD who are not adequately controlled by either a combination of an ICS and LABA or a LABA and LAMA. Currently, two triple combination therapies are available in the US: BREZTRI and TRELEGY ELLIPTA.

2020年7月,美國FDA批准了AstraZeneca的BREZTRI AEROSPHERE,用於COPD患者的維持治療。此外,2020年10月,TRIXEO AEROSPHERE(一種formoterol fumarate、glycopyrronium bromide和budesonide的組合)在歐盟獲得了治療成人中至重度COPD未被ICS和LABA組合或LABA和LAMA充分控制的患者的維持治療的營銷授權。目前,美國有兩種三聯療法可用:BREZTRI和TRELEGY ELLIPTA。

Learn more about the FDA-approved COPD drugs @ Drugs for COPD Treatment

了解更多關於FDA批准的COPD藥物@COPD治療藥物

Recently, Sanofi/Regeneron Pharmaceuticals' DUPIXENT added one more jewel to its crown by getting a label expansion nod for COPD from the FDA, EU, and NMPA. DUPIXENT's approval as the first targeted therapy for COPD represents a significant advancement in the treatment landscape for the disease. Unlike conventional treatments, which largely aim to manage symptoms, DUPIXENT specifically targets the IL-4 and IL-13 pathways linked to type 2 inflammation, a key driver in a subset of COPD patients. This precision in targeting allows for a more tailored treatment, especially for patients with elevated eosinophils, who often experience more frequent exacerbations and worse outcomes.

最近,賽諾菲/再生元製藥公司的DUPIXENt通過獲得FDA、歐盟和NMPA對COPD的標籤擴展認可,在其皇冠中再添一顆明珠。DUPIXENT作爲COPD的第一種靶向治療獲得批准,代表了該疾病治療格局中的重大進步。與主要旨在管理症狀的常規治療不同,DUPIXENt專門針對與第2型炎症相關的IL-4和IL-13通路,這是COPD患者亞組中的關鍵驅動因素。通過精準的靶向,特別適用於具有升高嗜酸性粒細胞的患者,這些患者經常出現更頻繁的惡化和更糟糕的預後。

The Phase III BOREAS trial demonstrated that patients treated with DUPIXENT experienced a 30% reduction in moderate-to-severe exacerbations over 52 weeks, significant improvements in lung function, and enhanced quality of life. By Week 52, those on DUPIXENT had improved prebronchodilator FEV1 by 160 mL compared to 77 mL in the placebo group. DUPIXENT was also well-tolerated, with a low frequency of adverse events. These results suggest that DUPIXENT could drastically shift COPD management by reducing exacerbations, improving lung function, and offering a safer, targeted therapy for patients with type 2 inflammation.

BOREAS第三期試驗表明,接受DUPIXENt治療的患者在52周內急性加重中有30%的減少,肺功能顯着改善,並且生活質量得到提高。到第52周,接受DUPIXENt治療的患者與安慰劑組相比,其慢阻肺支氣管舒前用藥後的FEV1改善了160毫升,而安慰劑組爲77毫升。DUPIXENt也具有良好的耐受性,不良事件發生頻率低。這些結果表明DUPIXENt可以通過減少急性加重、改善肺功能,併爲2型炎症患者提供更安全、更有針對性的治療,從而極大地改變COPD管理。

To know more about COPD treatment options, visit @ New Treatment for COPD

要了解更多關於COPD治療選擇,請訪問@ COPD新治療

The chronic obstructive pulmonary disease pipeline possesses potential drugs in mid-stage developments to be launched in the near future. Itepekimab (Sanofi/Regeneron Pharmaceuticals), Benralizumab (AstraZeneca), Tezepelumab (Amgen/AstraZeneca), Mepolizumab (GSK), and others shall further create a positive impact on the market.

慢性阻塞性肺疾病管線中具有潛力的候選藥物正在中期開發中,並將在不久的將來推出。Itepekimab(賽諾菲/再生元製藥公司),Benralizumab(阿斯利康),Tezepelumab(安進/阿斯利康),Mepolizumab(葛蘭素史克)等將進一步對市場產生積極影響。

Discover which therapies are expected to grab major COPD market share @ COPD Market Report

發現預期佔據重要COPD市場份額的治療方法@ COPD市場報告

Itepekimab is a fully human monoclonal antibody that targets interleukin-33 (IL-33), a protein involved in both type 1 and type 2 inflammation. The drug is administered via subcutaneous injection. Preclinical studies demonstrated that REGN3500 effectively inhibited several markers of both inflammatory types. Regeneron and Sanofi are investigating REGN3500 in diseases related to respiratory and dermatological inflammation. Currently, REGN3500 is in a Phase III clinical trial for COPD and was developed using Regeneron's VelocImmune technology, which produces optimized fully human antibodies. The development is part of a global collaboration between Regeneron and Sanofi.

Itepekimab是一種全人源單克隆抗體,靶向白細胞介素-33(IL-33),這是涉及1型和2型炎症的蛋白質。這種藥物通過皮下注射給予。臨床前研究表明,REGN3500有效抑制了若干種炎症類型的標誌物。再生元和賽諾菲正在研究REGN3500在與呼吸系統和皮膚炎症有關的疾病中的應用。目前,REGN3500正在進行用於COPD的第三期臨床試驗,並且是使用再生元的VelocImmune技術開發的,該技術生產優化的全人抗體。該研發項目是再生元和賽諾菲之間的全球合作的一部分。

FASENRA (benralizumab) is a humanized recombinant monoclonal antibody of the IgG1k immunoglobulin type that selectively targets the alpha chain of the interleukin 5 receptor (IL-5R) found on eosinophils and basophils. It prevents IL-5 from binding and stops the hetero-oligomerization of the IL-5R's alpha and beta subunits, thereby inhibiting signal transduction. Additionally, it is an afucosylated IgG, which enhances its affinity for the FcγRIIIα receptor on natural killer cells, macrophages, and neutrophils. Approved by the FDA in November 2017 for severe eosinophilic asthma, benralizumab was developed by MedImmune, AstraZeneca's global biologics R&D division. The company is currently conducting Phase III clinical trials for FASENRA as a treatment for COPD.

FASENRA(苯達唑單抗)是一種靶向嗜酸性粒細胞和嗜鹼性粒細胞上的白介素5受體(IL-5R)α鏈的人源重組單克隆抗體IgG0.1萬免疫球蛋白。它可以阻止IL-5結合,並阻止IL-5受體的α和β亞基的異源寡聚化,從而抑制信號轉導。此外,它是一種無核糖基化的IgG,增強了其對天然殺傷細胞、巨噬細胞和中性粒細胞上FcγRIIIα受體的親和力。FASENRA於2017年11月獲得FDA批准用於嚴重嗜酸性氣喘,是MedImmune開發的,也是阿斯利康全球生物製品研發部門的產品。該公司目前正在進行FASENRA作爲COPD治療的第三期臨床試驗。

TEZSPIRE (tezepelumab), a pioneering human monoclonal antibody created by Amgen and AstraZeneca, has shown considerable therapeutic potential for various respiratory conditions. Originally intended for treating COPD, TEZSPIRE has yielded encouraging results in decreasing moderate-to-severe exacerbations in patients with high blood eosinophil counts. Recent findings from the Phase IIa COURSE Trial, unveiled at the ATS 2024 conference, underscored TEZSPIRE's effectiveness in minimizing COPD exacerbations among patients with different eosinophil levels.

安進和阿斯利康研發的開多生物抗體藥物TEZSPIRE(tezepelumab)已顯示出在治療多種呼吸控件方面具有顯著的治療潛力。最初用於治療慢性阻塞性肺病(COPD),TEZSPIRE在降低高血液嗜酸性粒細胞計數患者中中至重度加劇方面取得了令人鼓舞的結果。最近在ATS 2024年年會上公佈的IIa期COURSE試驗結果強調了TEZSPIRE在減少不同嗜酸性粒細胞水平患者COPD加劇方面的有效性。

Mepolizumab is currently undergoing Phase III clinical trials for COPD, particularly in patients with frequent exacerbations and elevated eosinophil levels. It is available as an injectable solution and a powder for reconstitution for subcutaneous administration. The IL-5 receptor complex activates several signaling pathways that lead to the release of cytokines, neuromediators, chemokines, and various kinases, which facilitate eosinophil differentiation, proliferation, recruitment, and degranulation. Mepolizumab works by inhibiting the formation of the IL-5 receptor complex, thereby preventing eosinophil activation. This disruption affects normal eosinophil maturation and function, leading to decreased eosinophilic airway inflammation and reduced eosinophil survival.

Mepolizumab目前正在進行慢性阻塞性肺病(COPD)的III期臨床試驗,特別是針對頻繁加劇和嗜酸性粒細胞水平升高的患者。它可作爲可注射溶液和用於皮下注射重新構成的粉劑使用。IL-5受體複合物激活多條信號通路,導致細胞因子、神經介質、趨化因子和各種激酶的釋放,促進嗜酸性粒細胞的分化、增殖、招募和脫顆粒。Mepolizumab通過抑制IL-5受體複合物的形成而起到作用,從而防止嗜酸性粒細胞的激活。這種干擾影響了正常嗜酸性粒細胞的成熟和功能,導致了嗜酸性氣道炎症的減少和嗜酸性粒細胞存活的降低。

Discover more about drugs for COPD in development @ COPD Clinical Trials

在慢性阻塞性肺病(COPD)的藥物開發方面了解更多信息,請參閱COPD臨床試驗

The anticipated launch of these emerging therapies for COPD are poised to transform the market landscape in the coming years. As these cutting-edge therapies continue to mature and gain regulatory approval, they are expected to reshape the COPD market landscape, offering new standards of care and unlocking opportunities for medical innovation and economic growth.

預計這些新興的慢性阻塞性肺病治療方法的推出將在未來幾年改變市場格局。隨着這些前沿治療方法的不斷成熟和獲得監管批准,預計它們將重塑COPD市場格局,提供新的護理標準,併爲醫療創新和經濟增長開闢機會。

DelveInsight estimates that the market size for COPD in the 7MM is expected to grow from USD 16 billion in 2023 with a significant CAGR of 5% by 2034. This growth is mainly driven by the rise in the number of prevalent cases of COPD, ongoing clinical research, and better diagnostic tools that might improve the prognosis of the disease.

DelveInsight估計,到2034年,7Mm地區慢性阻塞性肺病市場規模預計將從2023年的160億美元增長,並且具有顯著的5%的複合年增長率。這種增長主要受慢性阻塞性肺病患病人數增加、持續的臨床研究以及可能改善該疾病預後的更好診斷工具的推動。

DelveInsight's latest published market report titled as Chronic Obstructive Pulmonary Disease Market Insight, Epidemiology, and Market Forecast – 2034 will help you to discover which market leader is going to capture the largest market share. The report provides comprehensive insights into the COPD country-specific treatment guidelines, patient pool analysis, and epidemiology forecast to help understand the key opportunities and assess the market's underlying potential. The COPD market report proffers epidemiological analysis for the study period 2020–2034 in the 7MM segmented into:

DelveInsight最新發布的市場報告,標題爲「慢性阻塞性肺病市場洞察,流行病學和市場預測-2034年」,將幫助您了解哪家市場領導者將奪得最大的市場份額。該報告全面深入地洞察了COPD特定國家的治療指南,患者群分析和流行病學預測,以幫助了解關鍵機遇並評估市場潛力。COPD市場報告提供了2020-2034年研究期間在7Mm片段內進行的流行病學分析:

  • Total Diagnosed Prevalent Cases of COPD
  • Subtype-specific Diagnosed Prevalent Cases of COPD
  • Gender-specific Diagnosed Prevalent Cases of COPD
  • Age-specific Diagnosed Prevalent Cases of COPD
  • Diagnosed Prevalent Cases of COPD Based on Severity of Airflow Limitation
  • Diagnosed Prevalent Cases of COPD Based on Symptoms and Exacerbation History
  • COPD總診斷患病率病例
  • COPD亞型特定診斷患病率病例
  • COPD性別特定診斷患病率病例
  • COPD年齡特定診斷患病率病例
  • 根據氣流受限程度的COPD診斷患病率病例
  • 根據症狀和急性加重史的COPD診斷患病率病例

The report provides an edge while developing business strategies by understanding trends shaping and driving the 7MM COPD market. Highlights include:

該報告通過了解形成和推動7Mm COPD市場的趨勢,爲制定商業策略提供了優勢。要點包括:

  • 11-year Forecast
  • 7MM Analysis
  • Epidemiology-based Market Forecasting
  • Historical and Forecasted Market Analysis upto 2034
  • Emerging Drug Market Uptake
  • Peak Sales Analysis
  • Key Cross Competition Analysis
  • Industry Expert's Opinion
  • Access and Reimbursement
  • 11年預測
  • 7MM分析
  • 基於流行病學的市場預測
  • 歷史和預測市場分析直到2034年
  • 新興藥物市場接受程度
  • 銷售高峰分析
  • 關鍵交叉競爭分析
  • 行業專家意見
  • 獲取與報銷

Download this COPD market report to assess the epidemiology forecasts, understand the patient journeys, know KOLs' opinions about the upcoming treatment paradigms, and determine the factors contributing to the shift in the COPD market. Also, stay abreast of the mitigating factors to improve your market position in the COPD therapeutic space.

下載這份COPD市場報告,評估流行病學預測,了解患者旅程,了解KOL對即將到來的治療範式的看法,並確定導致COPD市場變化的因素。此外,及時了解改善您在COPD治療領域市場地位的緩解因素。

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慢性阻塞性肺疾病(Pipeline)洞察-2024年報告提供了有關管道景觀的全面見解,包括臨床和非臨床階段產品的管道藥物概況,以及關鍵的COPD公司,包括賽諾菲安萬特,基耶西法瑪蘇瑞公司,美國聯合醫療,維羅納製藥股份有限公司,免疫製品公司,Yungjin Pharm. Co., Ltd.,Pulmotect, Inc., Tetherex Pharmaceutical, CSL Behring, 阿斯利康,諾華,基因技術,福泰製藥,EmeraMed,Afimmune,mereo biopharma,Synairgen,Adamis Pharmaceuticals,Quercegen Pharmaceuticals LLC,Regend Therapeutics,Meridigen Biotech Co., Ltd.,Pulmatrix,艾萊賽,葛蘭素史克,EpiEndo Pharmaceuticals,三生製藥,OmniSpirant,Foresee Pharmaceuticals,安進,Organicell Regenerative Medicine,arrowhead pharmaceuticals,ProterixBio,RS BioTherapeutics,MitoRx,C4X Discovery,Respiratorius,ARk biosciences,Incannex,GNI Pharma,Celon pharma,Alveolus Bio,Kinaset therapeutics,Landos Biopharma,Parion Sciences,KeyMed Biosciences,Bioneer corporation,AlgiPharma,Palobiofarma,Dimerix Bioscience,Glenmark Pharmaceuticals, 等。

Asthma Market

哮喘市場

Asthma Market Insights, Epidemiology, and Market Forecast – 2034 report delivers an in-depth understanding of the disease, historical and forecasted epidemiology, as well as the market trends, market drivers, market barriers, and key asthma companies including GlaxoSmithKline, 4D Pharma plc, AstraZeneca, Suzhou Connect Biopharmaceuticals, Avillion, Pearl Therapeutics, ARS Pharmaceuticals, Sinomab, Avalo Therapeutics, Kymab, Sanofi, Cumberland Pharmaceuticals, Genentech, Inc., among others.

哮喘市場洞察、流行病學和市場預測-2034年報告提供了對疾病、歷史和預測流行病學以及市場趨勢、市場驅動因素、市場障礙的深入了解,以及包括葛蘭素史克,4D Pharma股份有限公司,阿斯利康,蘇州康宏生物製藥,Avillion,Pearl Therapeutics,ARS Pharmaceuticals,Sinomab,Avalo Therapeutics,Kymab,賽諾菲,坎伯蘭藥業,基因技術公司等重要哮喘公司。

Asthma Pipeline

哮喘管道

Asthma Pipeline Insight – 2024 report provides comprehensive insights about the pipeline landscape, including clinical and non-clinical stage products, and the key asthma companies, including Jiangsu Hengrui Medicine, GlaxoSmithKline, Immunotek SL, AB Science, EMS, Avalo Therapeutics, Sunshine Guojian Pharmaceutical (Shanghai) Co., Ltd., ARS Pharmaceuticals, Sanofi, Zura Bio Ltd., AstraZeneca, EURRUS Biotech GmbH, T-Balance Therapeutics GmbH, Gossamer Bio, Aldeyra Therapeutics, Inc., Trio Medicines, Janssen Research & Development, Arrowhead Pharmaceuticals, Hoffman-La-Roche, GlaxoSmithKline, Biohaven Pharmaceutical, TAK-Circulator Co., Shanghai Hengrui Pharmaceutical, among others.

哮喘管道洞察-2024年報告提供了關於管道景觀的全面見解,包括臨床和非臨床階段的產品,以及關鍵的哮喘公司,包括江蘇恒瑞醫藥、葛蘭素史克、Immunotek SL、Ab Science、EMS、Avalo Therapeutics、三生國健藥業(上海)有限公司、ARS製藥、賽諾菲、尤拉生物有限公司、阿斯利康、EURRUS生物技術有限公司Balance Therapeutics GmbH、gossamer bio、Aldeyra Therapeutics、Inc.、三聯藥品、強生研發、arrowhead pharmaceuticals、羅氏製藥、葛蘭素史克、biohaven製藥、TAk-Circulator 公司、上海恒瑞製藥等。

Acute Respiratory Distress Syndrome Market

急性呼吸窘迫綜合徵市場

Acute Respiratory Distress Syndrome Market Insights, Epidemiology, and Market Forecast – 2034 report delivers an in-depth understanding of the disease, historical and forecasted epidemiology, as well as the market trends, market drivers, market barriers, and key ARDS companies, including MediciNova, Edesa Biotech, Light Chain Biosciences, Boehringer Ingelheim, Genentech, Windtree Therapeutics, Biomarck Pharmaceuticals, Athersys, Healios, Direct Biologics, Biohaven Pharmaceutical, Arch Biopartners, APEPTICO Forschung und Entwicklung GmbH, Staidson (Beijing) Biopharmaceuticals, Veru, Mesoblast Limited, Avalo Therapeutics, Pluristem Therapeutics, ILTOO Pharma, among others.

急性呼吸窘迫綜合徵市場洞察,流行病學和市場預測-2034年報告提供了對該疾病的深入了解,歷史及預測的流行病學,以及市場趨勢,市場驅動因素,市場壁壘和關鍵的ARDS公司,包括美第奇新星生物技術、Edesa Biotech、Light Chain Biosciences、Boehringer Ingelheim、Genentech、windtree therapeutics、Biomarck Pharmaceuticals、athersys、Healios、直接生物製品、biohaven製藥、Arch Biopartners、APEPTICO研究與開發有限公司、舒泰神(北京)生物製藥、維羅納、mesoblast有限公司、Avalo Therapeutics、Pluristem Therapeutics、ILTOO Pharma等。

About DelveInsight

關於DelveInsight

DelveInsight is a leading Business Consultant and Market Research firm focused exclusively on life sciences. It supports pharma companies by providing comprehensive end-to-end solutions to improve their performance. Get hassle-free access to all the healthcare and pharma market research reports through our subscription-based platform PharmDelve.

DelveInsight是專注於生命科學的領先商業顧問和市場研究公司。通過提供全面的端到端解決方案來支持製藥公司來提高他們的業績。通過我們的訂閱平台PharmDelve,輕鬆獲取所有醫療保健和製藥市場研究報告。

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來源:DelveInsight Business Research, LLP

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