ProQR Therapeutics to Host Virtual Analyst and Investor Event on December 11, 2024
ProQR Therapeutics to Host Virtual Analyst and Investor Event on December 11, 2024
LEIDEN, Netherlands & CAMBRIDGE, Mass., Dec. 05, 2024 (GLOBE NEWSWIRE) -- ProQR Therapeutics N.V. (Nasdaq: PRQR) (ProQR), a company dedicated to changing lives through transformative RNA therapies, today announced that the Company will host a virtual Analyst and Investor Event on Wednesday, December 11, 2024 from 10:00 am until approximately 12:30 pm EST, including an Analyst Q&A session with members of the ProQR Management Team.
萊頓,荷蘭與劍橋,美國,2024年12月5日(環球新聞)-- ProQR therapeutics N.V.(納斯達克:PRQR)(ProQR),一家致力於通過變革性RNA療法改變生活的公司,今天宣佈公司將在2024年12月11日(星期三)上午10:00至大約下午12:30(東部時間)舉辦一次虛擬分析師和投資者活動,包括與ProQR管理團隊成員的分析師問答環節。
During the event, ProQR will highlight its proprietary Axiomer ADAR-mediated RNA editing platform, along with updates on its pipeline of development candidates including data updates and next steps on its programs for NTCP and B4GALT1, AX-0810 and AX-1412. Presentations will feature members of the Management Team including Daniel A. de Boer, Founder and CEO, and Gerard Platenburg, Chief Scientific Officer; René Beukema, Chief Corporate Development Officer will also join the analyst Q&A session with the Management Team.
在活動期間,ProQR將重點介紹其自主研發的Axiomer ADAR介導的RNA編輯平台,以及其開發候選藥物管線的更新,包括NTCP和B4GALT1,AX-0810和AX-1412的數據顯示更新和後續步驟。演講將包括管理團隊成員的介紹,包括創始人兼首席執行官Daniel A. de Boer和首席科學官Gerard Platenburg;首席企業發展官René Beukema也將參與與管理團隊的分析師問答環節。
Additionally, the following speakers will present at the event:
此外,以下演講者將在活動中發言:
- Peter Beal, PhD, will share his perspectives on driving innovation in the ADAR field. Dr. Beal is a Professor in the Department of Chemistry at the University of California at Davis and Director of the NIH-funded UC Davis Chemical Biology Graduate Program and member of the Scientific Advisory Board at ProQR.
- Prof. Gideon Hirschfield, MA(Oxon) MB BChir (Cantab) FRCP PhD, a key opinion leader, will share his views on the unmet need in the field and the opportunity for AX-0810. He is Professor of Gastroenterology and Hepatology, Toronto Centre for Liver Disease.
- 彼得·比爾,博士,將分享他在ADAR領域推動創新的看法。比爾博士是加州大學戴維斯分校化學系的教授,也是美國國立衛生研究院資助的UC戴維斯化學生物學研究生項目的主任,並且是ProQR科學諮詢委員會的成員。
- 基甸·赫希菲爾德教授,MA(牛津大學)Mb BChir(劍橋大學)FRCP博士,作爲關鍵意見領袖,將分享他對這一領域未滿足需求以及AX-0810機會的看法。他是多倫多肝病中心的胃腸病學和肝病學教授。
More detailed biographies are available below.
更詳細的傳記信息請見下方。
Event Registration Details
活動註冊詳情
To register for the Investor and Analyst webcast (December 11, 2024), please click here. A live webcast of the event will be available under "Events" in the "Investors & Media" section of ProQR's website at .
要註冊投資者和分析師網絡研討會(2024年12月11日),請點擊此處。活動的實時網絡研討會將在ProQR網站的「投資者與媒體」部分的「活動」下提供。
To join via phone, participants may preregister to receive dedicated dial-in details to access the call via the following website:
要通過電話參與,參與者可以提前註冊以接收專用撥號詳細信息,通過以下網站訪問該看漲:
It is suggested that participants dial into the conference call 15 minutes prior to the scheduled start time to avoid any delays in attendance. An archived version of the webcast will be available for replay via ProQR's website for approximately 30 days following the event.
建議參與者在會議電話開始時間前15分鐘撥入,以避免出席時的任何延誤。活動結束後大約30天,ProQR的網站將提供網絡廣播的存檔版本,以供重播。
Speaker Biographies
發言人簡歷
Peter A. Beal, PhD
彼得·A·比爾,博士
Peter A. Beal is a Professor in the Department of Chemistry at the University of California at Davis and current Director of the NIH-funded UC Davis Chemical Biology Graduate Program. Research from the Beal laboratory has advanced understanding of the structures and mechanism of action for ADAR enzymes responsible for adenosine to inosine RNA editing in humans. Recently, this knowledge has been applied to the design of guiding oligonucleotides capable of directing ADARs to make edits that correct disease-causing mutations in the transcriptome. Targets include mutations in mRNAs associated with Rett syndrome, Alzheimer's disease and Parkinson's disease. Dr. Beal teaches organic chemistry at the undergraduate level and several classes in nucleic acids chemistry and chemical biology at the graduate level.
彼得·A·比爾是加州大學戴維斯分校化學系的教授,並且是美國國立衛生研究院資助的加州大學戴維斯化學生物學研究生項目的現任董事。比爾實驗室的研究推動了對ADAR酶結構及作用機制的理解,這些酶負責在人類中進行腺苷到肌苷的RNA編輯。最近,這些知識被應用於設計能夠引導ADAR進行編輯的導向寡核苷酸,從而糾正轉錄組中的致病突變。目標包括與雷特綜合症、阿爾茨海默病和帕金森病相關的mRNA突變。比爾博士在本科層次教授有機化學,並在研究生層次教授幾門核酸化學和化學生物學課程。
Prof. Gideon Hirschfield, MA(Oxon) MB BChir (Cantab) FRCP PhD
吉迪恩·赫爾希爾德教授,MA(牛津)Mb BChir(劍橋)FRCP 博士
Prof. Gideon M. Hirschfield is a distinguished clinician-scientist specializing in autoimmune liver diseases. He holds the Lily and Terry Horner Chair in Autoimmune Liver Disease Research at the Toronto Centre for Liver Disease, Toronto General Hospital, and serves as a Professor of Medicine in the Division of Gastroenterology at the University of Toronto.
吉迪恩·M·赫爾希爾德教授是一位傑出的臨床科學家,專注於自身免疫性肝疾病。他擔任多倫多肝病中心的莉莉和特里·霍納自身免疫性肝病研究主席,以及多倫多大學胃腸病學系的醫學教授。
Prof. Hirschfield earned his medical degree from the University of Cambridge in 1996 and completed his undergraduate studies at the University of Oxford in 1994. He was awarded a PhD from the University of London in 2006. His postgraduate training included positions at Hammersmith Hospital and Royal Brompton Hospital in London, as well as a fellowship in Toronto, Canada.
赫爾希爾德教授於1996年在劍橋大學獲得醫學學位,1994年在牛津大學完成本科學習。他於2006年獲得倫敦大學的博士學位。他的研究生培訓包括在哈默史密斯醫院和倫敦皇家布朗普頓醫院的職位,以及在加拿大多倫多的一個研究員職務。
An internationally recognized expert, Prof. Hirschfield has published over 200 peer-reviewed articles, including lead authorship in high-impact journals such as the New England Journal of Medicine, The Lancet, and Nature Genetics.
作爲國際公認的專家,赫爾希爾德教授發表了超過200篇同行評審文章,包括在《新英格蘭醫學雜誌》、《柳葉刀》和《自然遺傳學》等高影響力期刊上的主導作者。
His research focuses on advancing therapies for inflammatory liver diseases to prevent the need for transplantation
他的研究集中於推進炎症性肝病的療法,以防止需要進行移植。
About Axiomer
ProQR正在開拓下一代RNA鹼基編輯技術,名爲Axiomer,該技術有可能爲不同類型的疾病提供新的藥物類,即「編輯寡核苷酸」(EON),通過在人類細胞中存在的分子機器ADAR(RNA上的腺嘌呤去氨酸酶)的高度特異性和靶向方式介導RNA的單核苷酸改變,EON旨在招募和引導內源性表達的ADAR改變RNA中的腺嘌呤(A)爲肌醇(I)--肌醇轉譯爲鳥嘌呤(G)--將具有致病突變的RNA糾正爲正常(野生型)RNA,調節蛋白質表達或改變蛋白質以幫助預防或治療疾病。
ProQR is pioneering a next-generation RNA base editing technology called Axiomer, which could potentially yield a new class of medicines for diverse types of diseases. Axiomer "Editing Oligonucleotides", or EONs, mediate single nucleotide changes to RNA in a highly specific and targeted way using molecular machinery that is present in human cells called ADAR (Adenosine Deaminase Acting on RNA). Axiomer EONs are designed to recruit and direct endogenously expressed ADARs to change an Adenosine (A) to an Inosine (I) in the RNA – an Inosine is translated as a Guanosine (G) – correcting an RNA with a disease-causing mutation back to a normal (wild type) RNA, modulating protein expression, or altering a protein so that it will have a new function that helps prevent or treat disease.
ProQR正在開創一種名爲Axiomer的下一代RNA鹼基編輯技術,可能產生一類新型藥物,適用於各種類型的疾病。Axiomer「編輯寡核苷酸」或EONs以一種高度特異和有針對性的方式介導RNA中的單核苷酸變化,利用人類細胞中存在的稱爲ADAR(腺苷脫氨酶用於RNA)的分子機制。Axiomer EONs旨在招募和指導內源表達的ADARs,使RNA中的腺苷(A)變爲肌苷(I)- 肌苷被翻譯爲鳥苷(G)- 從而糾正具有致病突變的RNA至正常(野生型)RNA,調節蛋白表達,或改變蛋白使其具有新功能,有助於預防或治療疾病。
About ProQR
ProQR Therapeutics致力於通過創新RNA治療藥物改變患者的生活。 ProQR正在開創下一代RNA技術,稱爲Axiomer,利用細胞自身的ADAR編輯機制進行RNA特定單核苷酸編輯,以扭轉突變或調節蛋白質表達,併爲罕見和普遍存在的需求不滿足的疾病提供可能新的藥物類。基於我們獨特的專有RNA修復平台技術,我們正在考慮患者和家人的需要增加我們的項目組合。
ProQR Therapeutics is dedicated to changing lives through the creation of transformative RNA therapies. ProQR is pioneering a next-generation RNA technology called Axiomer, which uses a cell's own editing machinery called ADAR to make specific single nucleotide edits in RNA to reverse a mutation or modulate protein expression and could potentially yield a new class of medicines for both rare and prevalent diseases with unmet need. Based on our unique proprietary RNA repair platform technologies we are growing our pipeline with patients and loved ones in mind.
proqr therapeutics致力於通過創造變革性的RNA療法來改變生活。ProQR正在開創一種名爲Axiomer的下一代RNA技術,利用稱爲ADAR的細胞自身編輯機制,在RNA中進行特定單核苷酸編輯,以逆轉突變或調控蛋白表達,可能生產出一類新藥物,可用於罕見病和常見病種,滿足未被滿足的需求。根據我們獨特的專有RNA修復平台技術,我們正在考慮患者及其親人的需求,不斷擴展我們的產品線。
Learn more about ProQR at .
了解更多關於proqr的信息,請訪問 。
Forward Looking Statements
前瞻性聲明
This press release contains forward-looking statements. All statements other than statements of historical fact are forward-looking statements, which are often indicated by terms such as "continue," "anticipate," "believe," "could," "estimate," "expect," "goal," "intend," "look forward to", "may," "plan," "potential," "predict," "project," "should," "will," "would" and similar expressions. Such forward-looking statements include, but are not limited to, express and implied statements regarding this event, the potential of our technologies and product candidates, our business, technology, strategy, preclinical model data, our initial pipeline targets and the upcoming strategic priorities and milestones related thereto, our Axiomer platform, including the continued development and advancement of our Axiomer platform, the therapeutic potential of our Axiomer RNA editing oligonucleotides and product candidates, our development programs, including the timing, progress and results of our preclinical studies, clinical trials and other development activities, including the release of data related thereto, our business operations, as well as the timing of our clinical development. Forward-looking statements are based on management's beliefs and assumptions and on information available to management only as of the date of this press release. Our actual results could differ materially from those expressed or implied by these forward-looking statements for many reasons, including, without limitation, the risks, uncertainties and other factors in our filings made with the Securities and Exchange Commission, including certain sections of our annual report filed on Form 20-F. These risks and uncertainties include, among others, the cost, timing and results of preclinical studies and clinical trials and other development activities by us and our collaborative partners whose operations and activities may be slowed or halted shortage and pressure on supply and logistics on the global market; the likelihood of our preclinical and clinical programs being initiated and executed on timelines provided and reliance on our contract research organizations and predictability of timely enrollment of subjects and patients to advance our clinical trials and maintain their own operations; our reliance on contract manufacturers to supply materials for research and development and the risk of supply interruption from a contract manufacturer; the potential for future data to alter initial and preliminary results of early-stage clinical trials; the unpredictability of the duration and results of the regulatory review of applications or clearances that are necessary to initiate and continue to advance and progress our clinical programs; the ability to secure, maintain and realize the intended benefits of collaborations with partners, including the collaboration with Eli Lilly and Company; the possible impairment of, inability to obtain, and costs to obtain intellectual property rights; possible safety or efficacy concerns that could emerge as new data are generated in research and development; general business, operational, financial and accounting risks, and risks related to litigation and disputes with third parties; and risks related to macroeconomic conditions and market volatility resulting from global economic developments, geopolitical instability and conflicts. Given these risks, uncertainties, and other factors, you should not place undue reliance on these forward-looking statements, and we assume no obligation to update these forward-looking statements, even if new information becomes available in the future, except as required by law.
本新聞稿包含前瞻性聲明。除歷史事實陳述外,所有聲明均爲前瞻性聲明,通常通過諸如「繼續」、「預期」、「相信」、「可能」、「估計」、「期望」、「目標」、「打算」、「期待」、「可能」、「計劃」、「潛在」、「預測」、「項目」、「應該」、「將」、「會」、「會」等類似表達來指示。這些前瞻性聲明包括但不限於,就本事件、我們技術和產品候選者的潛力、我們的業務、科技、策略、臨床前模型數據、我們的初始管道目標,以及與此相關的即將到來的戰略優先事項和里程碑、我們的Axiomer平台,包括我們Axiomer平台的持續開發和進步、我們的Axiomer RNA編輯寡核苷酸和產品候選者的治療潛力、我們的開發項目,包括我們臨床前研究、臨床試驗和其他開發活動的時間、進展和結果(包括相關數據的發佈)的表達和隱含聲明。前瞻性聲明基於管理層的信念和假設,以及管理層在本新聞稿發佈日期可獲得的信息。我們的實際結果可能與這些前瞻性聲明所表達或隱含的結果有重大不同,原因包括但不限於風險、不確定性及其他因素,這些因素在我們向證券交易委員會的申報文件中有所詳細闡述,包括我們在20-F表格上提交的年報的某些部分。這些風險和不確定性包括但不限於,臨床前研究和臨床試驗的費用、時間和結果,以及我們和合作夥伴的其他開發活動,其運營和活動可能因供應和物流的短缺及全球市場的壓力而放慢或中止;我們臨床前和臨床項目按時啓動和執行的可能性,以及依賴於我們的醫藥外包概念和及時招生的可預測性,以推進我們的臨床試驗並維持自身的運營;我們依賴代工廠商提供研究和開發所需的材料,以及來自代工廠商的供應中斷風險;未來數據可能會改變早期臨床試驗的初步和初步結果的潛力;對監管申請或批准審查的持續時間和結果的不可預測性,這對於啓動、推進和進展我們的臨床項目是必要的;與包括禮來公司在內的合作伙伴合作以獲取、維持和實現預期好處的能力;獲得知識產權的可能障礙、能力和費用;可能在研發中產生的新數據可能出現的安全性或有效性問題;一般業務、運營、財務和會計風險,與第三方的訴訟和爭議相關的風險;以及由於全球經濟發展、地緣政治不穩定和衝突導致的宏觀經濟條件和市場波動的風險。考慮到這些風險、不確定性和其他因素,您不應對這些前瞻性聲明給予過度信賴,我們也不承擔更新這些前瞻性聲明的義務,即使未來有新信息出現,法律要求的情況除外。
ProQR Therapeutics N.V.
proqr therapeutics N.V.
Investor contact:
Sarah Kiely
ProQR Therapeutics N.V.
T: +1 617 599 6228
skiely@proqr.com
or
Peter Kelleher
LifeSci Advisors
T: +1 617 430 7579
pkelleher@lifesciadvisors.com
投資者聯繫人:
Sarah Kiely
proqr therapeutics N.V.
T: +1 617 599 6228
skiely@proqr.com
or
Peter Kelleher
LifeSci顧問
電話:+1 617 430 7579
pkelleher@lifesciadvisors.com
Media contact:
Robert Stanislaro
FTI Consulting
T: +1 212 850 5657
robert.stanislaro@fticonsulting.com
媒體聯繫人:
Robert Stanislaro
fti諮詢
電話:+1 212 850 5657
電子郵件:robert.stanislaro@fticonsulting.com