This week, Pfizer Inc (NYSE:PFE) revealed a new collaboration to unlock new therapeutic approaches. Its smaller European industry peer specialized in early detection of cancer, Mainz Biomed N.V. (NASDAQ:MYNZ) applied for Breakthrough Device Designation to the US Food and Drug Administration (FDA) for its revolutionary colorectal cancer (CRC) screening test, which subject to the review, would significantly accelerate the approval process.
Pfizer Enter A Drug Discovery Collaboration
Pfizer entered a multi-year partnership with Evotec to work together to advance scientific discovery for diseases with unmet need. Together with Evotec, Pfizer will focus on research for metabolic and infectious diseases. Everest chief business officer tated the company is honored to join Pfizer in focusing on diseases with severe unmet medical needsthat impact millions across the globe whose vital mechanism has been disrupted. Everest is excited to explore innovative therapies by supporting Pfizer with research and development activites at its facilities in France, a country praised for developing a strong biopharmaceutical ecosystem. Biopharmaceuticals are the new generation of complex medicines whose active substance is derived from a living source by using cutting-edge methods. In addition to its high quality research infrastructure, France ranks second in Europe for its development pipeline that consists of 584 products, according to France Biolead.
Mainz Biomed Seeking Breakthrough Device Designation
Mainz Biomed developed a non-invasive CRC test, ColoAlert. Prior to the FDA application, Mainz Biomed reported positive results from its clinical studies ColoFuture and eAArly Detect, as well as data from a pooled study including both the European and the US data, that showed sensitivity of 97% for CRC, as well as 88% for advanced adenomas which are precancerous lesions, with a specificity of 93%. ColoAlert is already being marketed across Europe, but the next-generation test includes novel mRNA biomarkers that will be used in the pivotal registration study titled ReconAAsense.
Along with its proprietary portfolio of mRNA biomarkers, Mainz Biomed complemented the Fecal Immunochemical Test (FIT) with an advanced AI and machine learning algorithm.
Besides providing an easy, non-invasive, at-home solution for CRC screening that is often avoided due to the inconvenience of colonoscopy, Mainz Biomed also went a step further by providing the opportunity to prevent CRC altogether by allowing the treatment of advanced adenoma before they advance to a cancerous state.
All in all, the above stories are examples of embracing emerging technology for good, which will undoubtedly also do good to their financials, if successful.
DISCLAIMER: This content is for informational purposes only. It is not intended as investing advice.
This article is from an unpaid external contributor. It does not represent Benzinga's reporting and has not been edited for content or accuracy.
本週,輝瑞公司(紐交所:PFE)揭示了一項新合作來解鎖新的治療方法。其較小的歐洲行業同行Mainz Biomed N.V. (納斯達克:MYNZ)專門從事癌症早期檢測,已向美國食品和藥物管理局(FDA)申請“突破性設備認定”,用於其革命性的結直腸癌(CRC)篩查測試,如果經過審查,將顯着加快批准進程。
輝瑞進入藥物發現合作關係
輝瑞已與Evotec建立了多年的合作伙伴關係,共同推進未滿足需求的疾病的科學發現。與Evotec一起,輝瑞將專注於代謝和傳染病研究。 Everest首席業務官表示,該公司很榮幸能夠加入輝瑞公司,專注於那些對全球數百萬人造成嚴重不滿足的醫療需求的疾病,其重要機制已被破壞。 Everest很高興能夠探索創新療法,通過在法國設施開展研究和開發活動來支持輝瑞,法國因發展強大的生物製藥生態系統而備受讚譽。生物製藥是複雜藥物的新一代,其活性物質是通過使用先進方法從來源於生命的衍生物中提取的。除了其高質量的研究基礎設施外,根據France Biolead的數據,法國在其由584種產品組成的開發管道中排名歐洲第二。
Mainz Biomed尋求突破性設備認定
Mainz Biomed開發了一種非侵入性結直腸癌測試ColoAlert。在申請FDA之前,Mainz Biomed報告了來自其臨床研究ColoFuture和eAArly Detect以及包括歐洲和美國數據在內的彙總研究的積極結果,這些結果顯示在CRC方面的敏感性爲97%,在癌前病變的先驅性癌症中爲88%,具有93%的特異性。 ColoAlert已在歐洲市場上銷售,但下一代測試包括新的mRNA生物標誌物,將用於名爲ReconAAsense的關鍵註冊研究中。
除了其專有的mRNA生物標誌物組合外,Mainz Biomed還將先進的AI和機器學習算法與Fecal Immunochemical Test(FIT)相結合。
除了提供一種易於非侵入性的在家CRC篩查解決方案,Mainz Biomed還更進一步,提供了通過治療先進的癌前病變阻止CRC的機會。
總的來說,以上故事是採用新興技術爲良好事物所做的例子,如果成功,無疑也將有益於其財務情況。
免責聲明:本內容僅供參考,不構成任何投資建議。
本文來自非報酬的外部投稿人。它不代表Benzinga的報道,並且沒有因爲內容或準確性而被編輯。