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href="/cms-news/pharmaceutical.html" style="color:#333;" data-v-53bbd022>Pharmazeutische Nachrichten</a> > </div> <div data-v-53bbd022>The Vanishing Rsv Vaccine: A Billion-dollar Market Shrinks</div>  </div> <div class="flex flex_b" data-v-b438853c><div class="cate_left" data-v-b438853c><div class="cont_box" data-v-b438853c><div class="for_fixed_cont" style="position:absolute;left:0px;top:0px;" data-v-b438853c><div class="detail_share" data-v-b438853c><span data-v-b438853c>— Teilen —</span> <ul data-v-b438853c><li data-v-b438853c><a href="https://www.facebook.com/sharer.php?u=&t=" target="_blank" data-v-b438853c><span class="facebook" data-v-b438853c></span></a></li> <li data-v-b438853c><a href="https://twitter.com/share?url=&text=" target="_blank" data-v-b438853c><span class="linkedin" data-v-b438853c></span></a></li> <li data-v-b438853c><a href="https://www.linkedin.com/shareArticle?mini=true&url=&title=" target="_blank" data-v-b438853c><span class="twitter" data-v-b438853c></span></a></li> <li data-v-b438853c><span class="weixin" data-v-b438853c></span></li></ul></div></div> <div data-v-b438853c><div class="detail_top" data-v-b438853c><h1 class="special_font" data-v-b438853c>The Vanishing RSV Vaccine: A Billion-Dollar Market Shrinks</h1> <div class="detail_es clearfix" data-v-b438853c><div class="detail_nt" data-v-b438853c><span data-v-b438853c>ECHEMI</span> <span data-v-b438853c>2024-08-02 17:30:45</span></div></div></div> <div class="detail_zhengwen" data-v-b438853c><span data-v-b438853c><p><span style="font-family: arial, helvetica, sans-serif; font-size: 18px; text-indent: 2em;">In the field of medical research and development in the past, RSV vaccine was known as a shining star in the pharmaceutical industry, and its market potential was placed high hopes by investors and experts, like an infinite blue ocean. Recent RSV vaccines market prospect, however, between quietly fading out, just like a sudden storm, will originally brilliant blown apart.</span></p> <p><span style="font-family: arial, helvetica, sans-serif; font-size: 18px;">This shift comes from the United States centers for disease control and prevention of RSV vaccination strategy significant adjustments. The primary target population for RSV vaccination was older than 60 years of age. However, the new recommendation Narrows RSV vaccination to people older than 75 years of age and certain high-risk groups between 60 and 74 years of age. Is the background of this change, clinical studies have found that RSV vaccines may be linked to a rare nervous system disease - gillan - there is a connection barrie syndrome (GBS). Data show that within 21 days after vaccination, significantly increased the risk of GBS, doubtless caused regulators deep concerns about the safety of the vaccine.</span></p> <p><span style="font-family: arial, helvetica, sans-serif; font-size: 18px;">From the market expectations of $30 billion and dropped to only 3 billion dollars of narrow space, RSV vaccines has experienced a dramatic reversal of the market prospects, it is not only a vivid reflection of the hardships of medical innovation, is also a profound warning of industry. Any product, no matter how outstanding, its innovative when it comes to security issues, are likely to face the sharp decline in public trust, which affects the market performance.</span></p> <p><span style="font-family: arial, helvetica, sans-serif; font-size: 18px;">For pharmaceutical companies, RSV vaccines is undoubtedly a heavy blow, it reveals the market potential in the pursuit of technology innovation and at the same time, can not ignore the potential safety hazard. The development of the pharmaceutical industry must find a balance between innovation and safety. Only in this way can we ensure the steady progress of medical technology and truly benefit human health.</span></p></span></div> <div class="detail_source" data-v-b438853c><span data-v-b438853c>Haftungsausschluss: ECHEMI behält sich das Recht der endgültigen Erklärung und Revision aller Informationen vor.</span></div> </div> <div class="other_news" data-v-b438853c><div class="items" data-v-b438853c><span data-v-b438853c>Vorherige:</span> <a href="/cms/2002558.html" data-v-b438853c><h3 class="special_font" data-v-b438853c>Unexpected Setback in Rare Disease Drug Development: Takeaways from Takeda's Phase 3 Trial Failure</h3></a></div> <div class="items" data-v-b438853c><span data-v-b438853c>Nächste:</span> <a href="/cms/2002556.html" data-v-b438853c><h3 class="special_font" data-v-b438853c>$8.7 Billion Deal! 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17:30:45",description:A,editor:y,content:"\u003Cp\u003E\u003Cspan style=\"font-family: arial, helvetica, sans-serif; font-size: 18px; text-indent: 2em;\"\u003EIn the field of medical research and development in the past, RSV vaccine was known as a shining star in the pharmaceutical industry, and its market potential was placed high hopes by investors and experts, like an infinite blue ocean. Recent RSV vaccines market prospect, however, between quietly fading out, just like a sudden storm, will originally brilliant blown apart.\u003C\u002Fspan\u003E\u003C\u002Fp\u003E\n\u003Cp\u003E\u003Cspan style=\"font-family: arial, helvetica, sans-serif; font-size: 18px;\"\u003EThis shift comes from the United States centers for disease control and prevention of RSV vaccination strategy significant adjustments. The primary target population for RSV vaccination was older than 60 years of age. However, the new recommendation Narrows RSV vaccination to people older than 75 years of age and certain high-risk groups between 60 and 74 years of age. Is the background of this change, clinical studies have found that RSV vaccines may be linked to a rare nervous system disease - gillan - there is a connection barrie syndrome (GBS). Data show that within 21 days after vaccination, significantly increased the risk of GBS, doubtless caused regulators deep concerns about the safety of the vaccine.\u003C\u002Fspan\u003E\u003C\u002Fp\u003E\n\u003Cp\u003E\u003Cspan style=\"font-family: arial, helvetica, sans-serif; font-size: 18px;\"\u003EFrom the market expectations of $30 billion and dropped to only 3 billion dollars of narrow space, RSV vaccines has experienced a dramatic reversal of the market prospects, it is not only a vivid reflection of the hardships of medical innovation, is also a profound warning of industry. Any product, no matter how outstanding, its innovative when it comes to security issues, are likely to face the sharp decline in public trust, which affects the market performance.\u003C\u002Fspan\u003E\u003C\u002Fp\u003E\n\u003Cp\u003E\u003Cspan style=\"font-family: arial, helvetica, sans-serif; font-size: 18px;\"\u003EFor pharmaceutical companies, RSV vaccines is undoubtedly a heavy blow, it reveals the market potential in the pursuit of technology innovation and at the same time, can not ignore the potential safety hazard. The development of the pharmaceutical industry must find a balance between innovation and safety. Only in this way can we ensure the steady progress of medical technology and truly benefit human health.\u003C\u002Fspan\u003E\u003C\u002Fp\u003E",source:z,exhibitionStartDate:a,exhibitionEndDate:a,country:a,city:a,cas:a,industry:a},prev:{contentid:D,catid:r,sourceid:s,catname:q,catUrl:t,catabbr:u,parentid:v,parentCatname:w,title:E,urlName:"unexpected-setback-in-rare-disease-drug-development-takeaways-from-takeda-s-phase-3-trial-failure",subtitle:c,tags:c,tagsArray:a,originalTags:c,thumb:F,published:x,publishedDatetime:"2024-08-02 17:31:00",description:"The results will undoubtedly bring takeda pharmaceuticals of new drug research and development of the road for a certain amount of uncertainty.",editor:y,content:"\u003Cp\u003E\u003Cspan style=\"font-family: arial, helvetica, sans-serif; font-size: 18px; text-indent: 2em;\"\u003ERecently, a well-known global takeda pharmaceuticals in its latest financial report revealed a regrettable news, which is developing the rare disease drug Soticlestat on two kinds of rare and refractory epilepsy type - and Lennox - Gastaut Dravet syndrome syndrome (LGS) the key phase III clinical trial, Failed to reach the expected effect of main goal. The results will undoubtedly bring takeda pharmaceuticals of new drug research and development of the road for a certain amount of uncertainty.\u003C\u002Fspan\u003E\u003C\u002Fp\u003E\n\u003Cp\u003E\u003Cspan style=\"font-family: arial, helvetica, sans-serif; font-size: 18px;\"\u003ESoticlestat has shown promising therapeutic potential and safety in early phase II trials, but the results of phase III trials have failed to replicate these positive signs. In SKYLINE test for Dravet syndrome patients, Soticlestat failed to significantly reduce the frequency of seizure epilepsy seizures, although in some secondary efficacy on indicators are still showing a certain clinical significance. In the SKYWAY trial, Soticlestat similarly did not significantly reduce the frequency of major motor drop seizures in patients with LGS.\u003C\u002Fspan\u003E\u003C\u002Fp\u003E\n\u003Cp\u003E\u003Cspan style=\"font-family: arial, helvetica, sans-serif; font-size: 18px;\"\u003ETakeda was undeterred by the results, which did not meet expectations. Company said that their potential indications of Soticlestat Dravet remained cautious optimism, with regulators and plan discussed in the complete clinical data, to determine the next step development strategy. However, Soticlestat accumulated hundreds of millions of dollars of losses in the process of r&d, undoubtedly has brought the financial position of the takeda extra pressure.\u003C\u002Fspan\u003E\u003C\u002Fp\u003E\n\u003Cp\u003E\u003Cspan style=\"font-family: arial, helvetica, sans-serif; font-size: 18px;\"\u003EDespite the challenges, Takeda's overall performance in the first quarter of fiscal 2021 remained strong. In the digestive tract tumor and rare diseases in the field of core product sales continue to maintain strong growth, new drug cefuroxime quetiapine for his excellent performance in the us market also has injected new vitality to the company's financial performance. These positive factors to make the industry for the future of takeda pharmaceuticals revenues and profits return to growth remain optimistic expectations.\u003C\u002Fspan\u003E\u003C\u002Fp\u003E\n\u003Cp\u003E\u003Cspan style=\"font-family: arial, helvetica, sans-serif; font-size: 18px;\"\u003EFor the frustrations of takeda pharmaceuticals in the Soticlestat test, we should be more understanding and tolerant attitude to look at. New drug research and development is a challenging process, even if is the industry leader is also hard to avoid failure. 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Given the intense scrutiny of pharmaceutical mergers by the Federal Trade Commission in recent years, the closing of the deal has been delayed until mid-2024.\u003C\u002Fspan\u003E\u003C\u002Fp\u003E\n\u003Cp\u003E\u003Cspan style=\"font-family: arial, helvetica, sans-serif; font-size: 18px;\"\u003EFor AbbVie, the acquisition has profound strategic implications. With its iconic products Humira patent is about to expire, companies need to find new sources of revenue to fill the possible income gap. Abbvie's neuroscience portfolio currently includes the antipsychotic drug Vraylar, as well as innovative migraine treatments Ubrelvy and Qulipta. According to data for the first half of 2024, these products brought AbbVie $4.127 billion in global net revenue, up 15.6% year over year, showing strong growth momentum.\u003C\u002Fspan\u003E\u003C\u002Fp\u003E\n\u003Cp\u003E\u003Cspan style=\"font-family: arial, helvetica, sans-serif; font-size: 18px;\"\u003ECerevel drug development pipeline is consists of a series for schizophrenia, epilepsy, Parkinson's and alzheimer's late candidate drugs, these drugs widely, is expected to be \"$1\" the potential of the product. 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