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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布新董事会主席及领导层任命
康乃德生物 ·  06/12 00:00
  • 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
  • 行业领导人Barry Quart,Pharm.D.被任命为首席执行官,接替郑炜博士,后者将继续担任董事会成员并担任顾问,协助过渡。
  • 经验丰富的生命科学高管David Szekeres被任命为总裁。
  • Kleanthis G. Xanthopoulos博士被任命为董事会主席。

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,加拿大圣地亚哥和中国太仓(环球新闻社)-全球临床阶段、总部位于美国的生物制药公司Connect Biopharma Holdings Ltd(Nasdaq:CNTB)(以下简称Connect或公司),宣布任命Barry Quart,Pharm.D.为首席执行官(CEO)兼董事,David Szekeres为总裁,Kleanthis G. Xanthopoulos,Ph.D.为董事会(董事会)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年以来一直担任董事会领先独立成员的Xanthopoulos博士已被任命为董事会主席。Xanthopoulos博士接替潘武斌博士,潘博士将在过渡期间继续担任董事会成员,并为公司提供顾问服务。

"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."

“代表董事会和Connect团队,我想感谢与郑炜博士和潘武斌博士共同创立Connect的愿景,并将下一代治疗药物带给患有炎症性疾病的患者和改善他们的生活。我们感谢他们为Connect使命所作的贡献和不懈的承诺,通过打造出具有第三阶段准备好的项目和强大的旗舰项目来构建出出色的组织。这些具有高度差异化的数据来自于哮喘和特应性皮炎的主要资产rademikibart阳性读数,在进入准商业阶段的美国驱动的后期公司方面塑造了Connect。我很高兴欢迎这支具有如此卓越的履历的新领导团队,并急于利用Barry的和David的操作专业知识和丰富的经验来释放rademikibart和其余管道的最大潜力/价值。” - Connect董事会主席Kleanthis G. Xanthopoulos,Ph.D.说。

"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."

“与Bill一起创立Connect并领导Connect,与许多热衷于发现和开发改变生命的药物的才华横溢的同事合作,在过去的12年里一直是一种真正的荣幸和特权。随着Connect发展到专注于推进rademikibart,Bill和我期待着支持Barry和David,因为Connect进入一个充满活力和新的阶段。” - Zheng Wei博士说。

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拥有超过30年的丰富经验,曾担任生物技术和制药公司的领导职务,开发了创新的药品产品。他个人领导过几家早期生物技术公司,通过美国食品和药物管理局(FDA)审批的药物达到9种。

"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."

“我很荣幸担任Connect的首席执行官并加入董事会。我对公司未来具有无比的期待,我相信rademikibart是Dupilumab的最佳竞争对手。”Barry Quart,Pharm.D.,Connect的首席执行官和董事说。“拥有我们管道中多个创新疗法、至少到2026年的现金流和具有美国丰富经验的扩大管理团队,我相信我们已经拥有了实现未来重要股东回报的所有因素。”

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。他于2012年开始担任CEO和董事,于2019年转任总裁兼首席执行官,并于2020年10月被任命为董事会主席。在Heron,Quart博士监督了四种药物的开发和批准:两种CINV(CINVANTI和SUSTOL)和两种急诊药物(ZYNRELEF和APONVIE)。在Heron之前,Quart博士于2006年创立了Ardea Biosciences,担任其总裁和首席执行官,并自从创立以来一直担任其董事,直到被阿斯利康PLC收购。在Ardea,Quart博士发明了一种治疗痛风的药物(ZURAMPIC)以及一系列MEK抑制剂的设计和开发,用于治疗癌症,并被拜耳AG许可。Quart博士目前担任Kiniksa Pharmaceuticals的董事会成员。他是18项美国专利的发明人,75篇出版物和摘要的作者。Quart博士获得了加利福尼亚大学旧金山分校的药学博士学位。David Szekeres是一位经验丰富的生命科学高管,具有深厚的操作、商业、公司发展/战略和法律专业知识,已证明能够创造价值。Szekeres先生最近担任快鹿治疗公司(heron therapeutics)的执行副总裁和首席运营官。在Heron之前,他是Regulus Therapeutics的首席业务官和首席法律顾问,Regulus Therapeutics是一家专注于RNA治疗的临床阶段生物技术公司,并曾担任Life Technologies Corporation的并购和收购领域负责人。Szekeres先生还担任GRI Bio,Inc.(Nasdaq:GRI)董事会主席,并担任CureMatch,Colossal Biosciences以及Sanford Burnham Prebys Medical Discovery Institute的董事会成员。他在杜克大学法学院获得J.D.学位,并在加利福尼亚大学欧文分校获得学士学位。和两种急性护理药物(ZYNRELEF和APONVIE),并且APONEVIE。在加入Heron之前,Quart博士是Ardea Biosciences,Inc.的创始人、总裁兼首席执行官和董事,从其成立到2012年阿斯利康公司收购。在Ardea,Quart博士发明并监督痛风药物(ZURAMPIC)的研发,以及设计和开发一系列MEK抑制剂用于癌症,并授权给拜耳公司。Quart博士目前担任Kiniksa Pharmaceuticals的董事会成员,拥有18项美国专利和75篇出版物和摘要。Quart博士在加利福尼亚大学旧金山分校获得药物博士学位。。

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是一家全球性临床阶段生物制药公司,应用其T细胞生物学专业知识和对药物发现行业的深入了解,开发创新疗法,治疗慢性炎症性疾病,旨在改善全球数百万受影响者的生活。该公司正在建立一系列专有的小分子和抗体管道,使用功能性T细胞分析,筛选和发现针对经过验证的免疫靶点的强烈的产品候选物。该公司的首席产品候选药物rademikibart(原名CBP-201)是一种抗体,旨在针对白细胞介素-4受体α(IL-4Rα)进行治疗特应性皮炎和哮喘。该公司的第二个产品候选药物icanbelimod(原名CBP-307)是S1P1 T细胞受体的调节剂,用于溃疡性结肠炎(UC)的治疗。欲知更多信息,请访问:

About Connect Biopharma Holdings Limited

关于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是一家全球临床阶段生物制药公司,应用其在T细胞生物学和药物发现行业的专业知识,开发创新疗法以治疗慢性炎症性疾病,以改善全球数百万受影响者的生活。该公司正在建立一个丰富的专有小分子和抗体管道,使用功能性T细胞测定,对经过验证的免疫靶点筛选和发现强效药物候选人。该公司的主导产品候选Rademikibart(以前称为CBP-201)是一种抗体,旨在靶向干扰素-4受体α(IL-4Rα),正在开发用于治疗特应性皮炎和哮喘。公司的第二个产品候选人Icanbelimod(以前称为CBP-307)是S1P1 T细胞受体调节剂,正在开发用于治疗溃疡性结肠炎(UC)。欲了解更多信息,请访问:https://www.connectbiopharm.com/

Forward-Looking Statements

前瞻性声明

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,本新闻稿中包含的非历史事实描述的陈述属于前瞻性陈述。诸如“可能”,“可能会”,“将”,“会”,“应该”,“期望”,“计划”,“预计”,“相信”,“估计”,“意图”,“预测”,“寻求”,“考虑”,“展望”,“潜力”,“继续”或“项目”或这些术语的否定形式或其他类似术语,均旨在识别前瞻性陈述。这些陈述包括公司推进其产品候选品开发的计划,实现任何开发、监管或商业里程碑或报告数据的时间或是否将实现或生成这些里程碑或数据,包括是否将提交或接受任何新药申请以及其时间,以及这些产品候选品的潜力,包括实现任何益处、改进、差异化、趋势或简介或产品批准或有效性,以及公司现金和投资支持计划业务运营的充足性。包含前瞻性陈述并不代表Connect Biopharma公司的任何计划将会实现。由于公司业务固有的风险和其他风险,以及公司提交给美国证券交易委员会(SEC)的文件中所描述的其他风险,本报告中设定的实际数据可能与此有所不同,包括公司于2024年4月16日提交给SEC的20-F年报和其他报告。投资者应注意,不应过度依赖这些前瞻性陈述,这些陈述仅于此日期有效,Connect Biopharma公司不承担修改或更新本新闻稿以反映此后事件或情况的义务。有关这些和其他风险的更多信息包含在Connect Biopharma公司提交给SEC的文件中,在SEC网站(www.sec.gov)和Connect Biopharma公司网站(www.connectbiopharm.com)“投资者”标题下提供。所有前瞻性陈述均在这一警示语句的整体中合格。此警示是根据1995年《私人证券诉讼改革法》第21E条安全港规定发布的。

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

投资者联系方式:
蒂姆·麦卡锡
LifeSci Advisors
tim@lifesciadvisors.com

声明:本内容仅用作提供资讯及教育之目的,不构成对任何特定投资或投资策略的推荐或认可。 更多信息
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