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Connect Biopharma Announces New Leadership and Chair of the Board of Directors

Connect Biopharma Announces New Leadership and Chair of the Board of Directors

康涅狄格州康涅狄格生物公司公佈新董事會主席及領導層任命
康乃德生物 ·  06/12 12:00
  • Industry leader Barry Quart, Pharm.D. appointed as Chief Executive Officer succeeding Zheng Wei, Ph.D., who will remain on the Board of Directors and serve as an advisor to assist with the transition
  • Experienced life science executive David Szekeres appointed as President
  • Kleanthis G. Xanthopoulos, Ph.D. appointed as Chair of the Board of Directors
  • 行業領導人Barry Quart,Pharm.D.被任命爲首席執行官,接替鄭煒博士,後者將繼續擔任董事會成員並擔任顧問,協助過渡。
  • 經驗豐富的生命科學高管David Szekeres被任命爲總裁。
  • Kleanthis G. Xanthopoulos博士被任命爲董事會主席。

SAN DIEGO, CA and TAICANG, China, June 12, 2024 (GLOBE NEWSWIRE) -- Connect Biopharma Holdings Limited (Nasdaq: CNTB) (Connect or the Company), a U.S.-headquartered, global clinical-stage biopharmaceutical company dedicated to improving the lives of patients with chronic inflammatory diseases through the development of therapies derived from T cell-driven research, announced today the appointments of Barry Quart, Pharm.D., as Chief Executive Officer (CEO) and Director, David Szekeres as President, and Kleanthis G. Xanthopoulos, Ph.D., as the new Chair of the Board of Directors (Board).

2024年6月12日,加拿大聖地亞哥和中國太倉(環球新聞社)-全球臨床階段、總部位於美國的生物製藥公司Connect Biopharma Holdings Ltd(Nasdaq:CNTB)(以下簡稱Connect或公司),宣佈任命Barry Quart,Pharm.D.爲首席執行官(CEO)兼董事,David Szekeres爲總裁,Kleanthis G. Xanthopoulos,Ph.D.爲董事會(董事會)的新主席。

Dr. Xanthopoulos, currently the lead independent member of the Board since 2022, has been appointed Chair of the Board. Dr. Xanthopoulos succeeds Wubin (Bill) Pan, Ph.D., M.B.A., who will remain on the Board and serve as an advisor to the Company during the transition.

自2022年以來一直擔任董事會領先獨立成員的Xanthopoulos博士已被任命爲董事會主席。Xanthopoulos博士接替潘武斌博士,潘博士將在過渡期間繼續擔任董事會成員,併爲公司提供顧問服務。

"On behalf of the board and the Connect team I would like to thank Drs. Zheng Wei and Wubin (Bill) Pan, who co-founded Connect with the vision to bring next-generation therapeutics to patients with inflammatory diseases and improve their lives. We are grateful for their contributions and unwavering commitment to the Connect mission by building an outstanding organization with Phase 3-ready programs and a robust pipeline," said Kleanthis G. Xanthopoulos, Ph.D., Chair of the Board of Directors of Connect. "The highly differentiated data generated from positive readouts in both asthma and atopic dermatitis for the lead asset, rademikibart, establishes Connect now as a U.S.-driven late-stage company entering its pre-commercial phase. I am thrilled to welcome the new leadership team with such an impressive track record and eager to leverage Barry's and David's operational expertise and wealth of experience to unlock the maximum potential/value of rademikibart and the rest of the pipeline."

“代表董事會和Connect團隊,我想感謝與鄭煒博士和潘武斌博士共同創立Connect的願景,並將下一代治療藥物帶給患有炎症性疾病的患者和改善他們的生活。我們感謝他們爲Connect使命所作的貢獻和不懈的承諾,通過打造出具有第三階段準備好的項目和強大的旗艦項目來構建出出色的組織。這些具有高度差異化的數據來自於哮喘和特應性皮炎的主要資產rademikibart陽性讀數,在進入準商業階段的美國驅動的後期公司方面塑造了Connect。我很高興歡迎這支具有如此卓越的履歷的新領導團隊,並急於利用Barry的和David的操作專業知識和豐富的經驗來釋放rademikibart和其餘管道的最大潛力/價值。” - Connect董事會主席Kleanthis G. Xanthopoulos,Ph.D.說。

"Founding and leading Connect with Bill and working with many talented colleagues who are passionate about discovery and development of life-changing medicines in the past 12 years has been a true honor and privilege," said Dr. Zheng Wei. "As Connect evolved to focus on advancing rademikibart, Bill and I look forward to supporting Barry and David as Connect enters an exciting new phase."

“與Bill一起創立Connect並領導Connect,與許多熱衷於發現和開發改變生命的藥物的才華橫溢的同事合作,在過去的12年裏一直是一種真正的榮幸和特權。隨着Connect發展到專注於推進rademikibart,Bill和我期待着支持Barry和David,因爲Connect進入一個充滿活力和新的階段。” - Zheng Wei博士說。

Dr. Barry Quart, the Company's newly appointed CEO, brings over 30 years of extensive experience serving in leadership positions in biotechnology and pharmaceutical companies and developing innovative pharmaceutical products. He has personally led several early-stage biotech companies through late-stage clinical development and regulatory strategy, highlighted by nine U.S. Food and Drug Administration (FDA) approved drugs.

Connect的新任CEO Barry Quart擁有超過30年的豐富經驗,曾擔任生物技術和製藥公司的領導職務,開發了創新的藥品產品。他個人領導過幾家早期生物技術公司,通過美國食品和藥物管理局(FDA)審批的藥物達到9種。

"I am honored to assume the CEO role for Connect and to join the Board. I am incredibly excited about the potential of the Company going forward with rademikibart, which I believe to be a best-in-class competitor to dupilumab," said Barry Quart, Pharm.D., CEO and Director of Connect. "With the multiple innovative therapies in our pipeline, a cash runway into at least 2026, and an expanded management team with proven experience in the U.S., I believe we have all the elements in place to achieve significant shareholder returns in the future."

“我很榮幸擔任Connect的首席執行官並加入董事會。我對公司未來具有無比的期待,我相信rademikibart是Dupilumab的最佳競爭對手。”Barry Quart,Pharm.D.,Connect的首席執行官和董事說。“擁有我們管道中多個創新療法、至少到2026年的現金流和具有美國豐富經驗的擴大管理團隊,我相信我們已經擁有了實現未來重要股東回報的所有因素。”

Dr. Quart was most recently CEO at Heron Therapeutics. He first served as CEO and Director starting in 2012, transitioned to President and CEO in 2019 and was named Chair of the Board in October 2020. At Heron, Dr. Quart oversaw the development and approval of four drugs: two drugs for CINV (CINVANTI and SUSTOL) and two acute care drugs (ZYNRELEF and APONVIE). Prior to Heron, Dr. Quart co-founded Ardea Biosciences, Inc. in 2006 and served as its President and Chief Executive Officer and Director from its inception through its acquisition by AstraZeneca PLC in 2012. At Ardea, Dr. Quart invented and oversaw the development of a drug for gout (ZURAMPIC), as well as the design and development of a series of MEK inhibitors for cancer that were licensed to Bayer AG. Dr. Quart currently serves on the Board of Directors of Kiniksa Pharmaceuticals. He is an inventor on 18 U.S. patents and an author on 75 publications and abstracts. Dr. Quart received his Pharm.D. from the University of California, San Francisco.

Quart博士最近是Heron Therapeutics的CEO。他於2012年開始擔任CEO和董事,於2019年轉任總裁兼首席執行官,並於2020年10月被任命爲董事會主席。在Heron,Quart博士監督了四種藥物的開發和批准:兩種CINV(CINVANTI和SUSTOL)和兩種急診藥物(ZYNRELEF和APONVIE)。在Heron之前,Quart博士於2006年創立了Ardea Biosciences,擔任其總裁和首席執行官,並自從創立以來一直擔任其董事,直到被阿斯利康PLC收購。在Ardea,Quart博士發明了一種治療痛風的藥物(ZURAMPIC)以及一系列MEK抑制劑的設計和開發,用於治療癌症,並被拜耳AG許可。Quart博士目前擔任Kiniksa Pharmaceuticals的董事會成員。他是18項美國專利的發明人,75篇出版物和摘要的作者。Quart博士獲得了加利福尼亞大學舊金山分校的藥學博士學位。David Szekeres是一位經驗豐富的生命科學高管,具有深厚的操作、商業、公司發展/戰略和法律專業知識,已證明能夠創造價值。Szekeres先生最近擔任快鹿治療公司(heron therapeutics)的執行副總裁和首席運營官。在Heron之前,他是Regulus Therapeutics的首席業務官和首席法律顧問,Regulus Therapeutics是一家專注於RNA治療的臨床階段生物技術公司,並曾擔任Life Technologies Corporation的併購和收購領域負責人。Szekeres先生還擔任GRI Bio,Inc.(Nasdaq:GRI)董事會主席,並擔任CureMatch,Colossal Biosciences以及Sanford Burnham Prebys Medical Discovery Institute的董事會成員。他在杜克大學法學院獲得J.D.學位,並在加利福尼亞大學歐文分校獲得學士學位。和兩種急性護理藥物(ZYNRELEF和APONVIE),並且APONEVIE。在加入Heron之前,Quart博士是Ardea Biosciences,Inc.的創始人、總裁兼首席執行官和董事,從其成立到2012年阿斯利康公司收購。在Ardea,Quart博士發明並監督痛風藥物(ZURAMPIC)的研發,以及設計和開發一系列MEK抑制劑用於癌症,並授權給拜耳公司。Quart博士目前擔任Kiniksa Pharmaceuticals的董事會成員,擁有18項美國專利和75篇出版物和摘要。Quart博士在加利福尼亞大學舊金山分校獲得藥物博士學位。。

David Szekeres is an experienced life science executive with a proven track record of creating value with deep operational, commercial, corporate development/strategy, and legal expertise. Mr. Szekeres was most recently Executive Vice President and Chief Operating Officer of Heron Therapeutics. Prior to Heron, he was the Chief Business Officer and General Counsel of Regulus Therapeutics, a clinical-stage biotech company focused on RNA therapeutics and the Head of Mergers & Acquisitions at Life Technologies Corporation. Mr. Szekeres also holds positions as the Chair of the Board of GRI Bio, Inc. (Nasdaq: GRI) and is a member of the Board of Directors of CureMatch, Colossal Biosciences, and the Sanford Burnham Prebys Medical Discovery Institute. He received his J.D. from Duke University School of Law and earned his B.A. at the University of California, Irvine.

Connect Biopharma是一家全球性臨床階段生物製藥公司,應用其T細胞生物學專業知識和對藥物發現行業的深入了解,開發創新療法,治療慢性炎症性疾病,旨在改善全球數百萬受影響者的生活。該公司正在建立一系列專有的小分子和抗體管道,使用功能性T細胞分析,篩選和發現針對經過驗證的免疫靶點的強烈的產品候選物。該公司的首席產品候選藥物rademikibart(原名CBP-201)是一種抗體,旨在針對白細胞介素-4受體α(IL-4Rα)進行治療特應性皮炎和哮喘。該公司的第二個產品候選藥物icanbelimod(原名CBP-307)是S1P1 T細胞受體的調節劑,用於潰瘍性結腸炎(UC)的治療。欲知更多信息,請訪問:

About Connect Biopharma Holdings Limited

關於Connect Biopharma Holdings Limited

Connect Biopharma is a global, clinical-stage biopharmaceutical company applying its expertise in T cell biology and deep knowledge of the drug discovery industry to develop innovative therapies to treat chronic inflammatory diseases with the goal of improving the lives of millions of those affected around the world. The Company is building a rich pipeline of proprietary small molecules and antibodies, using functional T cell assays, to screen and discover potent product candidates against validated immune targets. The Company's lead product candidate, rademikibart (formerly known as CBP-201), is an antibody designed to target interleukin-4 receptor alpha (IL-4Rα) in development for the treatment of atopic dermatitis and asthma. The Company's second product candidate, icanbelimod (formerly known as CBP-307), is a modulator of S1P1 T cell receptors and is in development for the treatment of ulcerative colitis (UC). For more information, please visit: https://www.connectbiopharm.com/

Connect Biopharma是一家全球臨床階段生物製藥公司,應用其在T細胞生物學和藥物發現行業的專業知識,開發創新療法以治療慢性炎症性疾病,以改善全球數百萬受影響者的生活。該公司正在建立一個豐富的專有小分子和抗體管道,使用功能性T細胞測定,對經過驗證的免疫靶點篩選和發現強效藥物候選人。該公司的主導產品候選Rademikibart(以前稱爲CBP-201)是一種抗體,旨在靶向干擾素-4受體α(IL-4Rα),正在開發用於治療特應性皮炎和哮喘。公司的第二個產品候選人Icanbelimod(以前稱爲CBP-307)是S1P1 T細胞受體調節劑,正在開發用於治療潰瘍性結腸炎(UC)。欲了解更多信息,請訪問:https://www.connectbiopharm.com/

Forward-Looking Statements

前瞻性聲明

Connect Biopharma cautions that statements included in this press release that are not a description of historical facts are forward-looking statements. Words such as "may", "could", "will", "would", "should", "expect", "plan", "anticipate", "believe", "estimate", "intend", "predict", "seek", "contemplate", "look forward", "potential", "continue" or "project" or the negative of these terms or other comparable terminology are intended to identify forward-looking statements. These statements include the Company's plans to advance the development of its product candidates, the timing of achieving any development, regulatory or commercial milestones or reporting data or whether such milestones or data will be achieved or generated, including whether any new drug application will be submitted or accepted and the timing thereof, and the potential of such product candidates, including to achieve any benefit, improvement, differentiation, trend or profile or any product approval or be effective, and the sufficiency of the Company's cash and investments to support planned operations. The inclusion of forward-looking statements should not be regarded as a representation by Connect Biopharma that any of its plans will be achieved. Actual data may differ materially from those set forth in this release due to the risks and uncertainties inherent in the Company's business and other risks described in the Company's filings with the Securities and Exchange Commission (SEC), including the Company's Annual Report on Form 20-F filed with the SEC on April 16, 2024, and its other reports. Investors are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date hereof, and Connect Biopharma undertakes no obligation to revise or update this news release to reflect events or circumstances after the date hereof. Further information regarding these and other risks is included in Connect Biopharma's filings with the SEC which are available from the SEC's website (www.sec.gov) and on Connect Biopharma's website (www.connectbiopharm.com) under the heading "Investors." All forward-looking statements are qualified in their entirety by this cautionary statement. This caution is made under the safe harbor provisions of Section 21E of the Private Securities Litigation Reform Act of 1995.

Connect Biopharma提醒,本新聞稿中包含的非歷史事實描述的陳述屬於前瞻性陳述。諸如“可能”,“可能會”,“將”,“會”,“應該”,“期望”,“計劃”,“預計”,“相信”,“估計”,“意圖”,“預測”,“尋求”,“考慮”,“展望”,“潛力”,“繼續”或“項目”或這些術語的否定形式或其他類似術語,均旨在識別前瞻性陳述。這些陳述包括公司推進其產品候選品開發的計劃,實現任何開發、監管或商業里程碑或報告數據的時間或是否將實現或生成這些里程碑或數據,包括是否將提交或接受任何新藥申請以及其時間,以及這些產品候選品的潛力,包括實現任何益處、改進、差異化、趨勢或簡介或產品批准或有效性,以及公司現金和投資支持計劃業務運營的充足性。包含前瞻性陳述並不代表Connect Biopharma公司的任何計劃將會實現。由於公司業務固有的風險和其他風險,以及公司提交給美國證券交易委員會(SEC)的文件中所描述的其他風險,本報告中設定的實際數據可能與此有所不同,包括公司於2024年4月16日提交給SEC的20-F年報和其他報告。投資者應注意,不應過度依賴這些前瞻性陳述,這些陳述僅於此日期有效,Connect Biopharma公司不承擔修改或更新本新聞稿以反映此後事件或情況的義務。有關這些和其他風險的更多信息包含在Connect Biopharma公司提交給SEC的文件中,在SEC網站(www.sec.gov)和Connect Biopharma公司網站(www.connectbiopharm.com)“投資者”標題下提供。所有前瞻性陳述均在這一警示語句的整體中合格。此警示是根據1995年《私人證券訴訟改革法》第21E條安全港規定發佈的。

INVESTOR CONTACT:
Tim McCarthy
LifeSci Advisors
tim@lifesciadvisors.com

投資者聯繫方式:
蒂姆·麥卡錫
LifeSci Advisors
tim@lifesciadvisors.com

譯文內容由第三人軟體翻譯。


以上內容僅用作資訊或教育之目的,不構成與富途相關的任何投資建議。富途竭力但無法保證上述全部內容的真實性、準確性和原創性。
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