展品99.3
网络直播的Cookie通信脚本
幻灯片1-JPM
· | 谢谢您,接线员 | |
· | 您好 -今天上午我们与TCR发布了一份联合新闻稿2 Treateutics-宣布与我们两家公司达成战略合作协议。 |
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· | 在第二份新闻稿中-我们提供了2022年第四季度和全年的财务和业务更新 | |
· | 我想 请您审阅前瞻性陈述的全文 | |
· | 我们 预计会在本次网络直播期间做出预测-由于几个因素,实际结果可能会大不相同 -包括我们提交给美国证券交易委员会的最新文件中概述的那些文件 以及我们将于今天晚些时候提交的截至2022年的10-K文件。 | |
· | 注意-我们将在此网络直播期间分享幻灯片-这些幻灯片也可以在我们IR网站的演示 选项卡上找到 | |
· | 我们的首席执行官禤浩焯和TCR的加里·门泽尔2Treatative的 总裁和首席执行官 以及Q&A 也在这里参加准备好的通话 | |
· | 到此为止,我将把电话转给禤浩焯·罗克利夫。Ad? |
幻灯片3-AD
· | 谢谢, 朱莉 | |
· | 我们 很高兴欢迎您参加本次网络直播,讨论我们两家公司的战略合作,这将创造一家治疗实体肿瘤的卓越细胞治疗公司 | |
· | 下一张幻灯片中列出了交易的详细信息 |
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· | 此 是以股换股的交易,根据该交易,Adaptimmune 股东将拥有合并后公司约75%的股份,而TCR²Treateutics股东将拥有合并后公司约25%的股份。 | |
· | 在关闭 并启用一系列催化剂后,这一 预计将把合并后的公司的跑道延长到2026年-我们将在后面讨论这一点 | |
· | 我将继续担任首席执行官,我们将拥有一个强大的董事会,成员来自Adaptimmune 和TCR2包括加里 | |
· | 我们 预计交易将在2023年第二季度完成-当然--还需得到股东的批准 | |
· | 该 是“什么?“我们正在做的是 | |
· | 然而, -今天电话的目的是要告诉你为什么我们正在做这件事,以及为什么我们对这种结合感到兴奋,特别是在这个时候-在细胞疗法的发展 中。 |
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网络直播的Cookie通信脚本
幻灯片5-AD
· | 以下是5个令人信服的理由“为什么”这种战略组合是正确的做法 | |
· | 首先, 我们是两家公司他们的整个历史聚焦于实体肿瘤 | |
· | 第二, 我们各自有一个强壮高度关注MAGE-A4和METHELIN计划的临床渠道,具有创造近期催化剂的重大价值 | |
· | 我们还有专注于PRAME和CD70…的中期临床前流程。 | |
· | 第三, 齐心协力--我们有一个创新的下一代工具箱,旨在增强我们产品在肿瘤微环境中的功能,同时我们的目标是开发既有疗效又有主流的细胞疗法 | |
· | 第四, 我们拥有端到端能力,因为两家公司完全致力于发现、开发和提供T细胞疗法 | |
· | 和 都拥有知识渊博、经验丰富的团队,他们成功地将这些疗法推进到了后期临床试验 | |
· | 最后, 和危急地-这种结合使我们能够要继续这一强大渠道的重点开发工作由于显著的运营优势,现金跑道将持续到2026年 | |
· | 我们 现在将在下面的幻灯片中更详细地讨论这五点 |
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· | Garry 和我以及我们的集体管理团队都相信,细胞疗法和基因疗法将对治疗领域产生可与25年前的克隆抗体相媲美的影响。 | |
· | 我们 相信这些疗法将实现转型癌症的治疗 | |
· | 但要做到这一点-他们显然-必须走出CAR-T和血液系统恶性肿瘤的狭窄范围--尽管如此,它们在2022年实现了近30亿美元的销售额-因为更大的机会在实体肿瘤的空间里 | |
· | 治疗实体肿瘤一直是Adaptimmune和TCR杰出员工毕生的工作2 | |
· | 我们在临床开发方面的计划包括领先者细胞疗法 实体瘤我们已经在多个癌症适应症中看到了强劲的应答率 | |
· | 临床上的这些T细胞疗法-以及其他落后的疗法--将使细胞疗法 完成这一格局的转变提供希望献给癌症患者 | |
· | 在宏观层面上,用细胞疗法治疗实体肿瘤是该行业的终极价值创造 论文。这就是我们公司存在的原因。利用管道的广度和跑道的深度获得这一机会 就是这种组合之所以有意义的原因 |
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· | 尽管恶性血液病只占美国所有癌症死亡的10%,但大多数细胞疗法和所有批准的CAR-T都集中在这些疾病上 | |
· | 但是 -90%的癌症死亡来自实体肿瘤,而这一空间在很大程度上还没有被细胞疗法所利用 | |
· | 我们断言,作为能够对肿瘤及其微环境产生反应的活药物,细胞疗法在治疗实体肿瘤方面具有明显的优势。 | |
· | 我相信我们合并后的公司将在这个快速增长和不断发展的领域拥有强大的领导地位 因为其互补的技术平台,Garry将会谈论到 |
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网络直播的Cookie通信脚本
幻灯片9--加里
· | 谢谢, 广告 | |
· | 正如广告所说,这是专注于实体肿瘤的细胞治疗的令人兴奋的时刻,许多癌症患者已经从临床试验中的治疗中受益 | |
· | 我们共同拥有互补的平台,使我们能够通过我们的SPAR和Truc T细胞疗法解决细胞内和细胞外 蛋白质靶点的广泛问题 | |
· | Adaptimmune专有的SPAR T细胞技术是基于T细胞受体--或TCR--的亲和力增强和工程设计,以特定靶标多肽:实体肿瘤上唯一表达的人类白细胞抗原复合体 | |
· | TCR2专利的Truc T细胞技术使用融合到TCR亚单位的基于抗体的结合域 来重新编程完整的TCR复合体来识别肿瘤表面抗原 | |
· | 这两项技术可以在合并后的公司的同种异体平台中进一步利用 | |
· | 有了Spear T细胞和Truc T细胞,我们有机会增加患者接受细胞治疗的机会。 | |
· | 广告? |
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· | 感谢 --Garry--有了这些互补的平台,我们正在优先考虑并专注于固体肿瘤领域细胞治疗的关键验证靶点 | |
· | 在多种肿瘤上表达的靶点 | |
· | 我们知道我们可以通过T细胞疗法解决的目标 | |
· | 在癌症中表达的靶点,每年导致30多万人死亡 | |
· | 我们 有机会通过我们针对这些靶点的重点渠道,使细胞治疗成为癌症患者的主流选择 |
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· | 我们针对这些靶点的 技术-实现了跨越多种不同癌症类型的深层管道 | |
· | 我们的领先临床项目将瞄准MAGE-A4和间皮质素 | |
· | 我们的临床前开发将专注于PRAME和CD70 | |
· | 正如Juli所描述的,这个渠道可以在网站上找到,所以我不会详细介绍 | |
· | 因为 我想把重点放在临床数据和我们相信将创造短期和中期价值的催化剂上 |
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网络直播的Cookie通信脚本
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· | 我们 从我们的两个领先特许经营权中获得了令人信服的临床疗效数据 | |
· | 有了afami-cel-我们正在按部就班地在2023年年中完成我们治疗滑膜肉瘤的BLA提交-这意味着可能在2024年批准首创针对实体瘤的TCRT细胞疗法 | |
· | 我们以MAGE-A4-ADP-A2M4CD8为靶点的下一代细胞疗法在我们的第一阶段信号发现试验中的总体应答率为37%,超过了广泛的实体肿瘤试验 | |
· | 在卵巢癌、膀胱癌和头颈癌中,我们发现有效率为52%-在这些肿瘤类型的患者中,接受过3次或更少先前治疗的患者的有效率进一步提高到75%。 | |
· | 展望未来-我们正在启动一线头颈癌和二线膀胱癌的新队列治疗,并联合使用培溴利珠单抗 | |
· | 以及 针对铂类耐药卵巢癌患者的2期试验--超越-3--我们打算将其注册 | |
· | Gavo-cel和下一代疗法-TC-510-靶向间硫蛋白--它也在多种癌症中表达 | |
· | 在第一阶段剂量发现试验中--几乎所有经过严格治疗的患者肿瘤消退,总有效率为22%。 | |
· | 在卵巢癌患者中,有效率接近30%。 | |
· | 展望未来--我们有潜力同时筛查卵巢癌患者的MAGE-A4和间充质蛋白,这将显著提高筛查成功率--这种联合开发是这一战略组合的显著操作优势之一 | |
· | Gavo-cel的第二阶段试验正在进行中,包括多剂量的选项以及与检查点抑制剂的组合,以潜在地提高响应率和持久性 | |
· | 针对间甲硫蛋白的下一代产品是TC-510,它采用了旨在提高效力的PD1:CD28开关 | |
· | 此 一期试验目前正在对一系列肿瘤进行剂量升级 | |
· | 在我们的联合计划中涉及安全问题 -我们的 材料中提供了更多详细信息,一般来说,我们看到的不良事件与淋巴枯竭和细胞治疗相关的不良事件是一致的,主要是不同水平的CRS 使用现有方法通常是可控和可逆的 | |
· | 总体而言, -到目前为止的收益-风险概况-是可以接受的。 |
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· | 交易完成后,合并后的公司预计将获得2026年的资金 | |
· | 我们 希望在融资的 窗口内通过这些计划提供多个创造价值的催化剂 | |
· | 以下是未来22个月您可以期待的事情的长长清单--当然,我们将继续 优化组合投资组合--做出数据驱动的资源分配决策 ,并专注于那些将带来最大价值的项目 |
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网络直播的Cookie通信脚本
· | 随着我们的资金现在延长到2026年,我们预计将在我们的资金窗口内从这些计划中提供多个重要的催化剂 | |
· | 以下是未来22个月你可以期待的事情的长长清单 | |
· | 我将在…上介绍以下几个项目 | |
· | 对于afami-cel,关键在于提交BLA和批准afami-cel的可能性。 | |
· | 对于 CD8增强-我们正在进行或正在启动试验,有可能在今明两年读出 | |
· | 首先 -用于晚期患者与检查点抑制剂的组合,以及一线头颈癌和二线膀胱癌的新队列 | |
· | 对于 Gavo-cel-稍后今年--我们预计首次从试验的第二阶段读出与nivolumab联合治疗铂耐药或难治性卵巢癌。 | |
· | 我们 还将有针对间皮瘤患者的年中读数-他们是在 焦点缩小到卵巢之前登记的-将包括有关检查点抑制剂影响的关键翻译数据 | |
· | 在2024年,我们预计在Gavo-cel试验中会有更多的读数 | |
· | 对于Gavo-cel的新一代版本TC-510,试验正在剂量升级 ,我们预计最初的安全性--然后潜在的疗效以及2024年的剂量发现 结果 | |
· | 和 PRAME和TC-520-目标是CD70-我们将在2023年和2024年将这些产品转移到Ind-Ready,正如这两家公司之前概述的那样 | |
· | 现在,我 想把它交给Garry来解释我们的一些下一代增强功能- 其中一些已经在我们的临床试验中使用 |
幻灯片13--加里
· | 谢谢, 广告 | |
· | 我们不仅有令人信服的临床数据和令人兴奋的临床前计划-我们还有一个工具箱来进一步增强我们的T细胞疗法 | |
· | 当 我们思考如何最好地使用T细胞疗法治疗实体瘤时-几个关键因素 起了作用我们的T细胞向实体瘤的运输、在充满敌意的肿瘤微环境中的持久性以及它们在那里的杀伤力 | |
· | 我们的CD8和PD-1 Switch下一代技术已经作为自体疗法进入临床 | |
· | 我们 还有许多其他的--例如IL-15和IL7/CCL19--可以投入战斗 | |
· | 和 -我们的互补技术平台最令人兴奋的方面之一是 针对多种抗原的能力 | |
· | 重要的是,所有这些方法也可以用于我们的同种异体平台 | |
· | 它不仅仅需要一个技术工具箱--它需要一套独特的功能才能使细胞疗法奏效--于是,我回到了广告 |
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网络直播的Cookie通信脚本
幻灯片14-AD
· | 谢谢, 加里 | |
· | 其中一个 实现这两家公司都有细胞疗法是一种真的独特的药品类别,并将复杂的技术转化为实际造福患者的产品 | |
· | 此 需要一组高度专业化的功能,需要紧密集成 以细胞疗法所特有的方式 | |
· | 我们的 合并公司一直专注于实体肿瘤的细胞治疗 | |
· | 我们 拥有经验丰富的团队,他们在该领域拥有久经考验的业绩记录 | |
· | 我们之间-我们已经将七个项目带入了诊所 | |
· | 其中五个 正在进行中,第一个用于工程TCR T细胞疗法的BLA将在今年提交 -由我们 | |
· | 我们在本幻灯片右侧为美国和英国概述的 功能包括不是偶然的而且它们不是可选的。 | |
· | 这些 功能是经过精心设计的建造起来-从地面开始由我们的每个公司 | |
· | 随着我们将互补的技术、团队和基础设施汇聚在一起,我们的目标是改变实体肿瘤的细胞治疗格局,因此将有重大的运营优势。 |
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· | 当交易完成时-我们将有现金到2026年 | |
· | 这 使我们能够为我之前展示的幻灯片上的催化剂。 | |
· | 作为一家合并后的公司,我们将继续专注于以数据驱动的方式投资合并后的资产负债表,从合并后的投资组合中创造最大价值 |
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· | 我想 以让这一战略组合具有吸引力的关键差异来结束 | |
· | 共同关注实体肿瘤-目前为止细胞治疗的最大机会 | |
· | 实体肿瘤令人信服的数据和临床进展-与我们现有的临床流水线 | |
· | 深入的临床前渠道,最初专注于PRAME和CD70 | |
· | Backed up by our expert teams and specialized end-to-end capabilities – a decade in the making | |
· | …And all made possible by our extended cash runway – we have the opportunity to deliver against our catalysts and against our ultimate goal of delivering transformative medicines to people with cancer | |
· | And - with that --- I’ll open up for questions --- operator? |
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COOKIE COMMS SCRIPT FOR WEBCAST
Forward-looking Statements
This communication relates to the proposed transaction pursuant to the terms of the Agreement and Plan of Merger, dated March 6, 2023, by and among Adaptimmune Therapeutics plc (“Parent”), CM Merger Sub, Inc. (“Merger Sub”), and TCR² Therapeutics Inc. (the “Company”). This communication includes express or implied forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), about the proposed transaction between the Company and Parent and the operations of the combined company that involve risks and uncertainties relating to future events and the future performance of Parent and the Company. Actual events or results may differ materially from these forward-looking statements. Words such as “will,” “could,” “would,” “should,” “expect,” “plan,” “anticipate,” “intend,” “believe,” “estimate,” “predict,” “project,” “potential,” “continue,” “future,” “opportunity” “will likely result,” “target,” variations of such words, and similar expressions or negatives of these words are intended to identify such forward-looking statements, although not all forward-looking statements contain these identifying words. Examples of such forward-looking statements include, but are not limited to, express or implied statements regarding: the business combination and related matters, including, but not limited to, satisfaction of closing conditions to the proposed transaction, prospective performance and opportunities with respect to Parent or the Company, post-closing operations and the outlook for the companies’ businesses; Parent’s, the Company’s or the combined company’s targets, plans, objectives or goals for future operations, including those related to Parent’s and the Company’s product candidates, research and development, product candidate introductions and product candidate approvals as well as cooperation in relation thereto; projections of or targets for revenues, costs, income (or loss), earnings per share, capital expenditures, dividends, capital structure, net financials and other financial measures; future economic performance, future actions and outcome of contingencies such as legal proceedings; and the assumptions underlying or relating to such statements.
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COOKIE COMMS SCRIPT FOR WEBCAST
These statements are based on Parent’s and the Company’s current plans, estimates and projections. By their very nature, forward-looking statements involve inherent risks and uncertainties, both general and specific. A number of important factors, including those described in this communication, could cause actual results to differ materially from those contemplated in any forward-looking statements. Factors that may affect future results and may cause these forward-looking statements to be inaccurate include, without limitation: uncertainties as to the timing for completion of the proposed transaction; uncertainties as to the Company’s and/or Parent’s ability to obtain the approval of Parent’s shareholders or the Company’s stockholders required to consummate the proposed transaction; the possibility that competing offers will be made by third parties; the occurrence of events that may give rise to a right of one or both of Parent and the Company to terminate the merger agreement; the possibility that various closing conditions for the proposed transaction may not be satisfied or waived on a timely basis or at all, including the possibility that a governmental entity may prohibit, delay, or refuse to grant approval, if required, for the consummation of the proposed transaction (or only grant approval subject to adverse conditions or limitations); the difficulty of predicting the timing or outcome of consents or regulatory approvals or actions, if any; the possibility that the proposed transaction may not be completed in the time frame expected by Parent and the Company, or at all; the risk that Parent and Company may not realize the anticipated benefits of the proposed transaction in the time frame expected, or at all; the effects of the proposed transaction on relationships with Parent’s or the Company’s employees, business or collaboration partners or governmental entities; the ability to retain and hire key personnel; potential adverse reactions or changes to business relationships resulting from the announcement or completion of the proposed transaction; significant or unexpected costs, charges or expenses resulting from the proposed transaction; the potential impact of unforeseen liabilities, future capital expenditures, revenues, costs, expenses, earnings, synergies, economic performance, indebtedness, financial condition and losses on the future prospects, business and management strategies for the management, expansion and growth of the combined business after the consummation of the proposed transaction; potential negative effects related to this announcement or the consummation of the proposed transaction on the market price of Parent’s American Depositary Shares or the Company’s common stock and/or Parent’s or the Company’s operating or financial results; uncertainties as to the long-term value of Parent’s American Depositary Shares (and the ordinary shares represented thereby), including the dilution caused by Parent’s issuance of additional American Depositary Shares (and the ordinary shares represented thereby) in connection with the proposed transaction; unknown liabilities related to Parent or the Company; the nature, cost and outcome of any litigation and other legal proceedings involving Parent, the Company or their respective directors, including any legal proceedings related to the proposed transaction; risks related to global as well as local political and economic conditions, including interest rate and currency exchange rate fluctuations; potential delays or failures related to research and/or development of Parent’s or the Company’s programs or product candidates; risks related to any loss of Parent’s or the Company’s patents or other intellectual property rights; any interruptions of the supply chain for raw materials or manufacturing for Parent or the Company’s product candidates, the nature, timing, cost and possible success and therapeutic applications of product candidates being developed by Parent, the Company and/or their respective collaborators or licensees; the extent to which the results from the research and development programs conducted by Parent, the Company, and/or their respective collaborators or licensees may be replicated in other studies and/or lead to advancement of product candidates to clinical trials, therapeutic applications, or regulatory approval; uncertainty of the utilization, market acceptance, and commercial success of Parent or the Company’s product candidates, and the impact of studies (whether conducted by Parent, the Company or others and whether mandated or voluntary) on any of the foregoing; unexpected breaches or terminations with respect to Parent’s or the Company’s material contracts or arrangements; risks related to competition for Parent’s or the Company’s product candidates; Parent’s or the Company’s ability to successfully develop or commercialize Parent’s or the Company’s product candidates; Parent’s, the Company’s, and their collaborators’ abilities to continue to conduct current and future developmental, preclinical and clinical programs; potential exposure to legal proceedings and investigations; risks related to changes in governmental laws and related interpretation thereof, including on reimbursement, intellectual property protection and regulatory controls on testing, approval, manufacturing, development or commercialization of any of Parent’s or the Company’s product candidates; unexpected increase in costs and expenses with respect to the potential transaction or Parent’s or the Company’s business or operations; and risks and uncertainties related to epidemics, pandemics or other public health crises and their impact on Parent’s and the Company’s respective businesses, operations, supply chain, patient enrollment and retention, preclinical and clinical trials, strategy, goals and anticipated milestones. While the foregoing list of factors presented here is considered representative, no list should be considered to be a complete statement of all potential risks and uncertainties. There can be no assurance that the proposed transaction or any other transaction described above will in fact be consummated in the manner described or at all. A more complete description of these and other material risks can be found in Parent’s and the Company’s respective filings with the U.S. Securities and Exchange Commission (the “SEC”), including each of their Annual Reports on Form 10-K for the year ended December 31, 2021, subsequent Quarterly Reports on Form 10-Q and other documents that may be filed from time to time with the SEC, as well as, the Registration Statement on Form S-4 which includes the joint proxy statement of Parent and the Company that also constitutes the prospectus of Parent, which joint proxy statement/prospectus will be mailed or otherwise disseminated to Parent’s shareholders and the Company’s stockholders when it becomes available. Parent and the Company also plan to file other relevant documents with the SEC regarding the proposed transaction.
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Any forward-looking statements speak only as of the date of this communication and are made based on the current beliefs and judgments of Parent’s and the Company’s management, and the reader is cautioned not to rely on any forward-looking statements made by Parent or the Company. Unless required by law, neither Parent nor the Company is under no duty and undertakes no obligation to update or revise any forward-looking statement after the distribution of this document, including without limitation any financial projection or guidance, whether as a result of new information, future events or otherwise.
No Offer or Solicitation
This communication is not intended to and shall not constitute an offer to subscribe for, buy or sell or the solicitation of an offer to subscribe for, buy or sell any securities, or a solicitation of any vote or approval, nor shall there be any sale of, or offer to sell or buy, securities in any jurisdiction in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such jurisdiction. This communication is for informational purposes only. No offering of securities shall be made, except by means of a prospectus meeting the requirements of Section 10 of the U.S. Securities Act of 1933, as amended, and otherwise in accordance with applicable law.
Additional Information and Where to Find It
In connection with the proposed transaction, Parent and the Company expect to file with the SEC a Registration Statement on Form S-4. The Registration Statement on Form S-4 will include a document that serves as a prospectus of Parent and a joint proxy statement of Parent and the Company, and each party may also file other documents regarding the proposed transaction with the SEC. INVESTORS AND SECURITY HOLDERS ARE URGED TO READ CAREFULLY THE REGISTRATION STATEMENT ON FORM S-4, JOINT PROXY STATEMENT/PROSPECTUS AND OTHER RELEVANT DOCUMENTS FILED OR WILL BE FILED WITH THE SEC, AS WELL AS ANY AMENDMENTS OR SUPPLEMENTS THERETO AND ANY DOCUMENTS INCORPORATED BY REFERENCE THEREIN, IN THEIR ENTIRETY IF AND WHEN THEY BECOME AVAILABLE BECAUSE THEY CONTAIN OR WILL CONTAIN IMPORTANT INFORMATION ABOUT THE PROPOSED TRANSACTION, RELATED MATTERS AND THE PARTIES TO THE PROPOSED TRANSACTION.
You may obtain a free copy of the Registration Statement on Form S-4, joint proxy statement/prospectus and other relevant documents (if and when they become available) that are or will be filed with the SEC for free at the SEC’s website at www.sec.gov. Copies of the documents filed with the SEC by the Company will be available free of charge on the Company’s website at https://investors.tcr2.com/ or by contacting the Company’s Investor Relations Department at https://investors.tcr2.com/contact-ir. Copies of the documents filed with the SEC by Parent will be available free of charge on Parent’s website at https://www.adaptimmune.com/investors-and-media or by contacting Parent’s Investor Relations Department at ir@adaptimmune.com.
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Participants in the Solicitation
Parent, the Company and certain of their respective directors and executive officers and other members of management and employees may be deemed to be participants in the solicitation of proxies in respect of the proposed transaction. Information about the directors and executive officers of Parent, including a description of their direct or indirect interests, by security holdings or otherwise, is set forth in Parent’s proxy statement for its 2022 Annual General Meeting, which was filed with the SEC on April 21, 2022, the Annual Report on Form 10-K for the year ended December 31, 2021 filed with the SEC on March 14, 2022, subsequent Quarterly Reports on Form 10-Q and other documents that may be filed from time to time with the SEC. Information about the directors and executive officers of the Company, including a description of their direct or indirect interests, by security holdings or otherwise, is set forth in the Company’s proxy statement for its 2022 Annual Meeting of Stockholders, which was filed with the SEC on September 1, 2022, the Annual Report on Form 10-K for the year ended December 31, 2021 filed with the SEC on March 22, 2022, subsequent Quarterly Reports on Form 10-Q and other documents that may be filed from time to time with the SEC. Other information regarding the participants in the proxy solicitations and a description of their direct and indirect interests, by security holdings or otherwise, will be contained in the joint proxy statement/prospectus included in the Registration Statement on Form S-4 and other relevant materials to be filed with the SEC regarding the proposed transaction when such materials become available. Security holders, potential investors and other readers should read the joint proxy statement/prospectus, included in the Registration Statement on Form S-4 carefully when it becomes available before making any voting or investment decision. You may obtain free copies of these documents from Parent or the Company using the sources indicated above.
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