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Vincerx Pharma to Implement Cost-Controls to Support Advancing Phase 1 Study of VIP943

Vincerx Pharma to Implement Cost-Controls to Support Advancing Phase 1 Study of VIP943

Vincerx制药公司将实施成本控制,以支持推进VIP943的第一阶段研究
GlobeNewswire ·  2024/12/04 06:45

Also Exploring Strategic Alternatives to Complement Fundraising Efforts

也正在探索战略替代方案,以补充筹款工作

PALO ALTO, Calif., Dec. 04, 2024 (GLOBE NEWSWIRE) -- Vincerx Pharma, Inc. (Nasdaq: VINC), a biopharmaceutical company aspiring to address the unmet medical needs of patients with cancer through paradigm-shifting therapeutics, today announced plans to implement cost-controls and explore strategic alternatives to support advancing the Phase 1 study of VIP943, the Company's novel CD123-targeted antibody-drug conjugate (ADC) developed with the Company's next-generation VersAptx platform.

加州帕洛阿尔托,2024年12月04日(环球社交媒体)—Vincerx Pharma, Inc.(纳斯达克股票代码:VINC),一家致力于通过开创性疗法解决癌症患者未满足医疗需求的生物制药公司,今天宣布计划实施成本控制措施,并探索战略替代方案,以支持推进VIP943阶段1研究的进行。VIP943是该公司使用下一代VersAptx平台开发的新型CD123靶向抗体药物结合物(ADC)

"We believe VIP943 is a highly differentiated and valuable asset, and we remain fully committed to advancing this program," said Ahmed Hamdy, M.D., Chief Executive Officer. "As we shared in October, the Phase 1 dose-escalation study of VIP943 has demonstrated encouraging safety, efficacy, and tolerability. Of nine evaluable patients, one patient whose acute myeloid leukemia (AML) relapsed post-transplant achieved a CRi and one patient with higher-risk myelodysplastic syndrome (HR-MDS) achieved a CRL. Notably, since October, the patient with CRi has continued to improve, with their most recent bone marrow results showing only 1% cancer cells. This patient has now been on the study for seven months and counting. Monotherapy responses in post-transplant patients are rare, so we believe this type of response highlights the potential of VIP943 in this challenging population and supports the next-generation technology of our VersAptx platform."

“我们认为VIP943是一项高度差异化且有价值的资产,我们会全力推动这个计划。”首席执行官Ahmed Hamdy万.D.表示。“正如我们在十月份分享的,VIP943的阶段1剂量递增研究显示了鼓舞人心的安全性、疗效和耐受性。在九位可评估的患者中,一位急性髓性白血病(AML)在移植后复发的患者实现了CRi,一位高风险骨髓增生异常综合征(HR-MDS)的患者实现了CRL。值得注意的是,自十月以来,CRi患者持续改善,最新的骨髓结果只显示1%的癌细胞。该患者目前已参与研究七个月并继续。移植后单药治疗患者的反应很少见,因此我们相信这种反应突出了VIP943在这一具有挑战性人群中的潜力,支持了我们VersAptx平台的下一代技术。”

Dr. Hamdy continued, "Our immediate focus is to give the program time to generate more data, with results from additional cohorts expected by early Q1 2025. To support this, we are implementing significant cost-cutting measures to focus resources on VIP943's advancement. Additionally, we will begin exploring strategic alternatives to complement our ongoing fundraising efforts, with the goal of maximizing the value of the VIP943 program and our VersAptx platform."

Hamdy博士继续说:“我们目前的重点是给这个项目更多的数据生成时间,预计到2025年第一季度初会有来自额外队列的结果。为了支持这一点,我们正在实施重大的削减成本措施,将资源集中在VIP943的推进上。此外,我们将开始探索战略替代方案,以补充我们正在进行的筹款工作,旨在最大限度地发挥VIP943项目和我们VersAptx平台的价值。”

As part of its review of potential strategic alternatives, Vincerx will consider options such as out-licensing, merger and acquisition opportunities, including reverse mergers, sales of assets and technologies, and other transactions. To streamline operations and focus resources, Vincerx will implement a significant reduction in force of approximately 55%. There can be no assurance that the exploration of strategic alternatives will result in any agreements or transactions, or as to the timing of any such agreements or transactions. The Company is in the process of engaging a financial advisor to assist in the strategic review process.

作为对潜在战略替代方案的审查的一部分,Vincerx将考虑诸如外部授权、合并和收购机会(包括反向合并)、资产和技术销售以及其他交易等选项。为了简化业务并集中资源,Vincerx将实施约55%的大幅裁员。无法保证对战略替代方案的探索将导致任何协议或交易,或关于任何此类协议或交易的时间安排。该公司正在与一家财务顾问合作,协助进行战略审查过程。

Vincerx has not set a timetable for completion of the evaluation process and does not intend to disclose further developments or guidance on the status of its exploration of strategic alternatives unless and until it is determined that further disclosure is appropriate or necessary.

Vincerx尚未设定评估进程完成的时间表,并无意透露进一步的发展或对战略替代方案的探索状态的指引,除非确定需要适当或必要的进一步披露。

As of October 31, 2024, the Company had approximately $8.4 million in cash, cash equivalents, and marketable securities.

截至2024年10月31日,公司在现金、现金等价物和有市场价值的证券方面约有840万美元。

About VIP943
VIP943, the first ADC from the VersAptx platform, consists of an anti-CD123 antibody, a unique linker cleaved intracellularly by legumain, and a novel kinesin spindle protein inhibitor (KSPi) payload enhanced with Vincerx's CellTrapper technology. Vincerx's proprietary effector chemistry (linker + payload) was designed to reduce non-specific release of the payload and ensure payload accumulation in cancer cells versus healthy cells. The increased therapeutic index has the potential to address challenges associated with many ADCs by improving efficacy and reducing severe toxicities. VIP943 is being evaluated in a Phase 1 dose-escalation trial in patients with relapsed/refractory AML, HR-MDS, and B-ALL who have exhausted standard therapeutic options (NCT06034275).

关于VIP943
VIP943是VersAptx平台中首个ADC,包含抗CD123抗体、一种被legumain细胞内切割的独特连接物以及一个由Vincerx的CellTrapper技术增强的新型肽酰蛋白酶A(KSPi)负荷。Vincerx专有的效应化学物质(连接物+负荷)旨在减少荷载的非特异性释放,并确保荷载在癌细胞中与健康细胞相比的堆积。增加的治疗指数有潜力解决许多ADC所面临的挑战,通过提高疗效并减少严重毒性。VIP943正在接受在已耗尽标准治疗方案的复发/难治性AML、HR-MDS和b-ALL患者中进行第一阶段剂量递增试验的评估(NCT06034275)。

About VersAptx Platform
VersAptx is a versatile and adaptable next-generation bioconjugation platform. The modular nature of this innovative platform allows the combination of different targeting, linker, and payload technologies to develop bespoke bioconjugates that address different cancer biologies. With this platform, (i) antibodies and small molecules can be used to target different tumor antigens, (ii) linkers can be designed to reduce non-specific release of the payload, cleave intracellularly or extracellularly, and conjugate to single or multiple payloads, and (iii) payloads can be designed with reduced permeability using our CellTrapper technology to ensure accumulation in cancer cells or to be permeable for release in the tumor microenvironment. The VersAptx platform allows the development of bioconjugates designed to address the safety and efficacy challenges of historical ADCs.

关于VersAptx平台
VersAptx是一种多功能且适应性强的下一代生物共轭平台。这一创新平台的模块化特性允许结合不同的靶向、连接剂和载荷技术,开发定制的生物共轭物质,以应对不同的癌症生物学特征。使用此平台,(i)可以利用抗体和小分子靶向不同的肿瘤抗原,(ii)连接剂可设计用于减少药物的非特异性释放,细胞内或细胞外裂解,并连接到单个或多个载荷,(iii)可使用我们的CellTrapper技术设计具有降低渗透性的载荷,以确保在癌细胞中积累或在肿瘤微环境中释放。VersAptx平台允许开发旨在解决历史ADC药物的安全性和有效性挑战的生物共轭物质。

About Vincerx Pharma, Inc.
Vincerx Pharma, Inc. is a clinical-stage biopharmaceutical company committed to developing differentiated and novel therapies to address the unmet medical needs of patients with cancer. Vincerx has assembled a seasoned management team with a proven track record of successful oncology drug development, approvals, and value creation. Vincerx's diverse pipeline consists of a next-generation antibody drug conjugate (ADC) VIP943, currently in Phase 1; a small molecule drug conjugate VIP236, which has completed its Phase 1; a CDK9 inhibitor enitociclib, which has completed a Phase 1 monotherapy study and continues in a Phase 1 study in collaboration with the NIH; a preclinical ADC VIP924; and VersAptx, a versatile, next-generation bioconjugation platform.

关于Vincerx Pharma,Inc。
Vincerx Pharma,Inc.是一家临床阶段生物制药公司,致力于开发不同iated和新颖的治疗方案,以满足患有癌症的患者的医疗需求。Vincerx已经组建了一个经验丰富的管理团队,他们在成功的肿瘤药物开发,批准和价值创造方面拥有卓越的记录。Vincerx的多样化产品线包括下一代抗体药物与毒素结合物(ADC) VIP943,目前处于第1期;一种完成了第1期的小分子药物结合物VIP236;一种CDK9抑制剂enitociclib,已完成第1期单药研究,继续与NIH合作进行第1期研究;一种预临床ADC VIP924;以及VersAptx,一个多功能的、下一代的生物结合平台。

Vincerx is based in Palo Alto, California, and has a research subsidiary in Monheim, Germany.

Vincerx总部位于加利福尼亚州的帕洛阿尔托,并在德国蒙海姆拥有一个研究子公司。

Forward-Looking Statements

前瞻性声明

This press release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended (the Securities Act), and Section 21E of the Securities Exchange Act of 1934, as amended, that are intended to be covered by the "safe harbor" created by those sections. Forward-looking statements, which are based on certain assumptions and describe future plans, strategies, expectations and events, can generally be identified by the use of forward-looking terms such as "believe," "expect," "may," "will," "should," "would," "could," "suggest," "seek," "intend," "plan," "goal," "potential," "on-target," "on track," "project," "estimate," "anticipate," or other comparable terms. All statements other than statements of historical facts included in this press release are forward-looking statements. Forward-looking statements include, but are not limited to, plans, timing, and disclosure regarding strategic alternatives, product candidates and attributes, expectations regarding advancement, development, timing, and results of product candidates, and engagement of a financial advisor. Forward-looking statements are neither historical facts nor assurances of future performance or events. Instead, they are based only on current beliefs, expectations, and assumptions regarding future business developments, future plans and strategies, projections, anticipated events and trends, the economy, and other future conditions. Forward-looking statements are subject to inherent uncertainties, risks, and changes in circumstances that are difficult to predict, many of which are outside Vincerx's control.

本新闻稿包含根据1933年修正《证券法》(以下简称证券法第27A条),以及1934年修正《证券交易法》(以下简称证券交易法第21E条)制定的有关前瞻性语句,这些语句旨在受到该等条款所创造的“安全港”的保护。基于某些假设并描述未来计划、策略、期望和事件的前瞻性语句,通常可通过使用前瞻性术语识别,例如“相信”,“期望”,“可能”,“将”,“应”,“会”,“可能”,“建议”,“寻求”,“打算”,“计划”,“目标”,“潜力”,“符合预期”,“按计划进行”,“同轨”,“项目”,“估计”,“预期”,或其他类似术语。本新闻稿中除了历史事实陈述之外的所有陈述均属于前瞻性陈述。前瞻性陈述包括但不限于有关战略选择、产品候选者和属性的计划、时间安排和披露,关于推进、开发、时间安排和产品候选者结果以及财务顾问参与等方面的期望。前瞻性陈述既非历史事实,也非对未来绩效或事件的担保,而仅基于当前信念、期望和假设,涉及未来业务发展、未来计划和策略、投射、预期事件和趋势、经济状况以及其他未来状况方面。前瞻性陈述受到难以预测的固有不确定性、风险和环境变化的影响,其中许多风险超出Vincerx的控制范围。

Actual results, conditions, and events may differ materially from those indicated in the forward-looking statements. Therefore, you should not rely on any of these forward-looking statements. Important factors that could cause actual results, conditions, and events to differ materially from those indicated in the forward-looking statements include, but are not limited to, Vincerx's capital requirements and availability and sufficiency of capital; Vincerx's ability to continue as a going concern; risks that Vincerx's activities to evaluate and pursue potential strategic alternatives may not result in a transaction that enhances stockholder value on a timely basis or at all; risks related to Vincerx's ability to reduce its expenses, and costs and expenses related to its streamlined operating plan; risks associated with clinical development of Vincerx's product candidates; general economic, financial, legal, political, and business conditions; and the risks and uncertainties set forth in the Form 10-Q for the quarter ended September 30, 2024 and subsequent reports filed with the Securities and Exchange Commission by Vincerx. Forward-looking statements speak only as of the date hereof, and Vincerx disclaims any obligation to update any forward-looking statements.

实际结果、状况和事件可能与前瞻性陈述所示不同。因此,您不应依赖任何这些前瞻性陈述。引起实际结果、状况和事件与前瞻性陈述所示不同的重要因素包括但不限于,Vincerx的资本需求及资本的可用性和充足性;Vincerx继续作为持续经营的能力;Vincerx评估和追求潜在战略选择的活动可能不会及时或完全导致增强股东价值的交易的风险;与Vincerx降低开支、以及与其简化运营计划相关的成本和费用的风险;与Vincerx产品候选者的临床开发相关的风险;一般经济、金融、法律、政治和商业状况;以及Vincerx提交给美国证券交易委员会的2024年9月30日季度10-Q表格和后续报告中列出的风险和不确定因素。前瞻性陈述仅于本日期具有效力,Vincerx不承担更新任何前瞻性陈述的义务。

Vincerx, the Vincerx logo, CellTrapper, and VersAptx are trademarks of Vincerx.

Vincerx、 Vincerx logo、 CellTrapper 和 VersAptx 是 Vincerx 的商标。

Contacts:
Gabriela Jairala
Vincerx Pharma, Inc.
gabriela.jairala@vincerx.com

联系人:
Gabriela Jairala
Vincerx Pharma,Inc.
gabriela.jairala@vincerx.com

Totyana Simien
Inizio Evoke Comms
totyana.simien@inizioevoke.com

Totyana Simien
Inizio Evoke Comms
totyana.simien@inizioevoke.com


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