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Palisade Bio Appoints Brian Feagan, MD, FRCPC, to Its Clinical Advisory Board

Palisade Bio Appoints Brian Feagan, MD, FRCPC, to Its Clinical Advisory Board

Palisade Bio 任命 Brian Feagan, MD, FRCPC, 为其临床顾问委员会成员
GlobeNewswire ·  2024/12/17 21:30

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Palisade Bio Appoints Brian Feagan, MD, FRCPC, to its Clinical Advisory Board
Palisade Bio任命Brian Feagan博士为其临床顾问委员会成员

Carlsbad, CA, Dec. 17, 2024 (GLOBE NEWSWIRE) -- Palisade Bio, Inc. (Nasdaq: PALI) ("Palisade," "Palisade Bio" or the "Company"), a clinical-stage biopharmaceutical company focused on developing novel therapeutics for patients with autoimmune, inflammatory, and fibrotic diseases, today announced the appointment of Brian G. Feagan, MD, FRCPC, to its Clinical Advisory Board.

加利福尼亚州卡尔斯巴德,2024年12月17日(环球新闻通讯)—— Palisade Bio, Inc.(纳斯达克:PALI)("Palisade," "Palisade Bio"或"公司"),是一家专注于为自体免疫性、炎症性和纤维化疾病患者开发新型治疗药物的临床阶段生物制药公司,今天宣布任命Brian G. Feagan博士为其临床顾问委员会成员。

Dr. Feagan is a distinguished gastroenterologist with over 30 years of experience in the design, conduct, and execution of large-scale randomized controlled trials (RCTs) for Crohn's disease (CD) and ulcerative colitis (UC). He has served as Principal Investigator in more than 140 multi-center RCTs and has dedicated much of his career to developing, validating, and optimizing outcome measures to evaluate the efficacy of novel therapeutics in CD and UC.

Feagan博士是一位杰出的胃肠病专家,在克罗恩病(CD)和溃疡性结肠炎(UC)的大规模随机对照试验(RCTs)的设计、实施和执行方面拥有超过30年的经验。他曾担任140多项多中心RCT的首席研究员,并且将职业生涯中的很多时间致力于开发、验证和优化结果指标,以评估新型治疗药物在CD和UC中的疗效。

"We are thrilled to welcome Dr. Feagan to our Clinical Advisory Board," said JD Finley, Chief Executive Officer of Palisade Bio. "Dr. Feagan's extensive research experience in CD and UC, along with his deep expertise in clinical trial design, will be invaluable as we advance the development of our next-generation precision therapies, beginning with PALI-2108 for the treatment of ulcerative colitis."

Palisade Bio首席执行官JD Finley表示:"我们非常高兴欢迎Feagan博士加入我们的临床顾问委员会。" 他补充道:"Feagan博士在CD和UC方面丰富的研究经验,加上他在临床试验设计方面的深厚专长,将对我们推动下一代精准治疗药物的发展至关重要,首个将是用于治疗溃疡性结肠炎的PALI-2108。"

Dr. Feagan commented, "Patients and clinicians are increasingly seeking oral treatment options that are more effective, safe and well-tolerated. PALI-2108's localized bioactivation holds the potential to address the tolerability issues associated with systemic distribution of this class of therapeutics. I look forward to collaborating with the Company to explore the most effective strategies for demonstrating clinical efficacy and advancing the development of this promising candidate, which targets significant unmet medical needs."

费根博士评论道:“患者和临床医生越来越多地寻求更有效、安全和耐受性更好的口服治疗选项。PALI-2108的局部生物激活有潜力解决与这一类疗法的系统分布相关的耐受性问题。我期待与公司合作,探索展示临床疗效和推进这一有前途候选药物(这款药物针对显著的未满足医疗需求)的最有效策略。”

Brian G. Feagan, MD, FRCPC

布赖恩·G·费根,医学博士,FRCPC

Dr. Feagan currently serves as a Professor of Medicine at the Schulich School of Medicine & Dentistry at the University of Western Ontario, a gastroenterologist at London Health Sciences Centre in Ontario, Canada, and the Senior Scientific Director of Alimentiv, Inc. A Fellow of the Royal College of Physicians and Surgeons of Canada, Dr. Feagan holds membership in the Canadian and American Association of Gastroenterology, the American College of Gastroenterology, the College of Physicians and Surgeons of Ontario, Crohn's and Colitis Canada (CCC) and European Crohn's and Colitis Organization (ECCO). Over the course of his career, he has authored over 480 articles and book chapters and has given over 600 invited presentations at national and international scientific meetings. In 1997, Dr. Feagan became Director of Robarts Clinical Trials at the Robarts Research Institute, University of Western Ontario and in 2020, he became Senior Scientific Director of Alimentiv Inc. (formerly Robarts Clinical Trials).

费根博士目前担任西安大略大学舒利赫医学院和牙科学院的医学教授,加拿大安大略省伦敦健康科学中心的胃肠病学家,以及Alimentiv, Inc.的高级科学主任。作为加拿大皇家医学会和外科医生学院的会员,费根博士还加入了加拿大和美国胃肠病学协会、美国胃肠病学会、安大略省医师和外科医生学院、克罗恩病和结肠炎加拿大(CCC)及欧洲克罗恩病和结肠炎组织(ECCO)。在他的职业生涯中,他撰写了超过480篇文章和书籍章节,并在国内外科学会议上进行了超过600次的受邀演讲。1997年,费根博士成为西安大略大学Robarts临床试验主任,2020年,他成为Alimentiv Inc.(前身为Robarts临床试验)的高级科学主任。

Dr. Feagan completed a medical degree at the University of Western Ontario (UWO) in London, Ontario, Canada. His postdoctoral training included a residency in Internal Medicine and a clinical fellowship in Gastroenterology in the Department of Medicine at UWO, and postgraduate training in the Department of Epidemiology and Biostatistics at McMaster University, Hamilton, Ontario.

费根博士在加拿大安大略省伦敦的西安大略大学(UWO)获得医学学位。他的博士后培训包括在UWO内科的住院医师训练和胃肠病学的临床研究员培训,以及在安大略省汉密尔顿的麦克马斯特大学流行病学和生物统计学系的研究生培训。

About Palisade Bio

关于Palisade Bio

Palisade Bio is a clinical-stage biopharmaceutical company focused on developing and advancing novel therapeutics for patients living with autoimmune, inflammatory, and fibrotic diseases. The Company believes that by using a targeted approach with its novel therapeutics it will transform the treatment landscape. For more information, please go to .

Palisade Bio是一家处于临床阶段的生物制药公司,专注于为患有自身免疫、炎症和纤维化疾病的患者开发和推广新型疗法。公司认为,通过使用其新型疗法的针对性方法,将会改变治疗格局。欲了解更多信息,请访问 .

Forward Looking Statements

前瞻性声明

This communication contains "forward-looking" statements for purposes of the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. Forward-looking statements include statements regarding the Company's intentions, beliefs, projections, outlook, analyses or current expectations concerning, among other things: the extent of our cash runway; our ability to successfully develop our licensed technologies; the timing and outcome of our current and anticipated applications and studies related to our product candidates; estimates about the size and growth potential of the markets for our product candidates, and our ability to serve those markets, including any potential revenue generated; future regulatory, judicial, and legislative changes or developments in the United States (U.S.) and foreign countries and the impact of these changes; our ability to maintain the Nasdaq listing of our securities; our ability to build a commercial infrastructure in the U.S. and other markets; our ability to compete effectively in a competitive industry; our ability to identify and qualify manufacturers to provide API and manufacture drug product; our ability to enter into commercial supply agreements; the success of competing technologies that are or may become available; our ability to attract and retain key scientific or management personnel; the accuracy of our estimates regarding expenses, future revenues, capital requirements and needs for additional financing; our ability to obtain funding for our operations; our ability to attract collaborators and strategic partnerships; and the impact of any global event on our business, and operations, and supply. Any statements contained in this communication that are not statements of historical fact may be deemed to be forward-looking statements. These forward-looking statements are based upon the Company's current expectations. Forward-looking statements involve risks and uncertainties. The Company's actual results and the timing of events could differ materially from those anticipated in such forward-looking statements as a result of these risks and uncertainties, which include, without limitation, the Company's ability to advance its nonclinical and clinical programs, the uncertain and time-consuming regulatory approval process; and the Company's ability to secure additional financing to fund future operations and development of its product candidates. Additional risks and uncertainties can be found in the Company's Annual Report on Form 10-K for the fiscal year ended December 31, 2023, filed with the Securities and Exchange Commission ("SEC") on March 26, 2024, and the Quarterly Reports on Form 10-Q or other SEC filings that are filed thereafter. These forward-looking statements speak only as of the date hereof, and the Company expressly disclaims any obligation or undertaking to release publicly any updates or revisions to any forward-looking statements contained herein to reflect any change in the Company's expectations with regard thereto or any change in events, conditions or circumstances on which any such statements are based.

本次通信包含《1995年私人证券诉讼改革法案》安全港条款所指的“前瞻性”陈述。前瞻性陈述包括有关公司的意图、信念、预测、展望、分析或当前对以下方面的预期:我们的现金流持续时间的程度;我们成功开发所持有技术的能力;我们当前和预计的申请及研究与我们的产品候选者的时间和结果;关于我们的产品候选者市场的规模和增长潜力估计,以及我们服务这些市场的能力,包括可能产生的营业收入;美国及其他国家未来的监管、司法和立法变更或发展及这些变化的影响;我们保持纳斯达克证券上市的能力;我们在美国及其他市场建立商业基础设施的能力;我们在竞争激烈的行业中有效竞争的能力;我们识别和资格认证制造商以提供API和生产药物产品的能力;我们进入商业供应协议的能力;竞争技术的成功,这些技术已经或可能推出;我们吸引和留住关键科学或管理人员的能力;我们关于费用、未来营业收入、资金需求和额外融资需求的估算的准确性;我们获得运营资金的能力;我们吸引合作者和战略伙伴关系的能力;以及任何全球事件对我们的业务、运营和供应的影响。本次通信中包含的任何非历史事实声明可能被视为前瞻性陈述。这些前瞻性陈述基于公司的当前预期。前瞻性陈述涉及风险和不确定性。公司的实际结果和事件的时间可能与预期的前瞻性陈述存在实质性差异,原因包括但不限于公司推动其非临床和临床项目的能力、监管批准程序的不确定性和耗时;以及公司确保额外融资以资助未来运营和产品候选者开发的能力。有关更多风险和不确定性信息,请参见公司于2023年12月31日结束的财政年度提交给证券交易委员会(“SEC”)的表格10-K年度报告,以及随后的表格10-Q季度报告或其他SEC文件。这些前瞻性陈述仅在本日期发言,并且公司明确否认任何公开发布本声明中包含的前瞻性陈述的更新或修订的义务或承诺,以反映公司在这方面的预期变化或任何此类陈述所依据的事件、条件或情况的变化。

Investor Relations Contact
JTC Team, LLC
Jenene Thomas
908-824-0775
PALI@jtcir.com

投资者关系联系人
JTC团队,有限责任公司
詹妮娜·托马斯
908-824-0775
PALI@jtcir.com

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