CD112R

关注并星标CPHI制药在线近日，先声药业发布公告宣布其注射用苏维西塔单抗的上市申请获NMPA受理，适应症为：联合化疗用于治疗含铂化疗治疗失败的复发性卵巢癌、输卵管癌或原发性腹膜癌。       苏维西塔单抗由先声药业与Apexigen公司合作开发，是一款新一代重组人源化抗VEGF兔源单克隆抗体。临床前研究显示：同剂量下苏维西塔单抗在多个肿瘤模型中表现出比贝伐珠单抗更优抑瘤效果和相似毒性。       2024年1月，先声药业宣布苏维西塔单抗联合化疗用于含铂化疗方案治疗失败的复发性上皮卵巢癌、输卵管癌和原发性腹膜癌患者的3期临床试验SCORES达到主要研究终点--对比安慰剂联合化疗组，苏维西塔单抗组PFS显示出具有统计学意义和临床意义的改善，且在所有亚组均显示出PFS临床获益的一致性。此外，关键次要终点OS的数据尚未成熟，但苏维西塔单抗组显示出获益的趋势。安全性方面，苏维西塔单抗安全性可控，未出现新的安全性信号。       卵巢癌是妇科肿瘤中病死率最高的恶性肿瘤，据悉2020年中国卵巢癌新发病例高达5.53万例，死亡病例达3.75万例。因起病隐匿，以及缺乏早期筛查手段，约70%的卵巢癌患者发现时已处于晚期。手术联合含铂化疗加减靶向维持治疗（如PARPi±贝伐珠单抗）是目前卵巢癌的主要治疗方式，但大多数患者会复发并最终进展为铂类耐药。铂耐药复发的卵巢癌患者预后差，且治疗选择有限。       贝伐珠单抗也是一款抗VEGF单抗，但AURELIA研究结果显示：贝伐珠单抗联合化疗可延长铂耐药复发卵巢癌患者的无进展生存（PFS）（化疗+贝伐珠单抗组6.7个月vs.化疗组3.4个月），但不能延长总生存期（OS）。而且，安全性分析发现贝伐珠单抗可导致高血压、蛋白尿及消化道穿孔的发生率增加。       与贝伐珠单抗相比，苏维西塔单抗联合化疗不仅可以延长铂耐药复发卵巢癌的PFS，还可以延长OS。苏维西塔单抗有望成为我国第一个适用于铂耐药卵巢癌患者的抗VEGF单抗。证券公司预测，若顺利获批，苏维西塔单抗2030年有望实现14.2亿销售额。       先声药业肿瘤研发管线分析       先声药业作为传统综合性制药龙头企业，现专注于向创新研发转型，研发管线主要涉及肿瘤、中枢神经系统和自身免疫三大领域。在肿瘤领域，先声药业已有三款产品获批上市，如曲拉西利、恩沃利单抗和恩度®️（重组人血管内皮抑制素注射液）。       曲拉西利是先声药业从G1 Therapeutics公司引进的细胞周期蛋白依赖性激酶4和6(CDK4/6)抑制剂，2022年7月在国内被NMPA批准用于既往未接受过系统性化疗的广泛期小细胞肺癌（ES-SCLC）患者，在接受含铂类药物联合依托泊苷方案治疗前给药，以降低化疗引起的骨髓抑制的发生率。而且，曲拉西利还于2023年9月在国内申报新适应症，用于ES-SCLC患者在接受含拓扑替康方案治疗前给药，以降低化疗引起的骨髓抑制的发生率。       恩沃利单抗是先声药业于2020年引进的一款皮下注射用PD-L1 抗体，先声药业拥有其在中国大陆的独家商业推广权。目前，该药已于2021年11月被NMPA批准用于治疗不可切除或转移性微卫星高度不稳定(MSI-H)或错配修复基因缺陷型(dMMR)的成人晚期实体瘤。       恩度是国内第一个获批的抗血管生成靶向药，也是国内外唯一获准销售的内皮抑制素，2005年9月被批准联合NP化疗方案用于治疗初治或复治的Ⅲ/Ⅳ期非小细胞肺癌患者。       此外，先声药业肿瘤研发管线还有多款新药，详见下表。整体来看，先声药业在研肿瘤药物大多处于临床前和1期临床。而且，这些药物除了从外部企业引进，还有多款是先声药业自主研发。       其中多西他赛聚合物胶束是先声药业于2020年9月从苏州海特比奥生物技术有限公司引进。该药以两亲性生物相容性可降解材料聚乙二醇单甲醚聚乳酸嵌段聚合物（mPEG-PDLLA）作为增溶载体，大大提高了稳定性，并降低了配制要求，更方便临床使用。已完成的1期临床试验结果显示：多西他赛胶束在25mg/m2~100mg/m2范围内，患者均可耐受， 75mg/m2剂量组7例疗效可评估，其中2例部分缓解，2例疾病稳定，100mg/m2剂量组5例疗效可评估，均为疾病稳定。       SIM0395（paxalisib）是先声药业从Kazia Therapeutics Limited引进的一款可透过血脑屏障的PI3K/mTOR通路抑制剂，拟用于治疗胶质母细胞瘤（GBM）。已公布的2期临床试验的中期数据显示，paxalisib可延长MGMT非甲基化的新发GBM患者的PFS和OS。2021年12月，该药在国内获批临床。       SIM0270是先声药业旗下子公司先声再明原研的一款新型可透脑选择性雌激素受体降解剂（SERD），在首次人体1期临床中对经多线治疗失败的晚期或转移性ER+/HER2-乳腺癌患者展现出良好的耐受性和抗肿瘤活性。在第46届圣安东尼奥乳腺癌研讨会上公布的SIM0270单药和/或与哌柏西利或依维莫司联合治疗HR+/HER2-晚期或转移性乳腺癌的1a期临床试验数据显示：在50名疗效可评估患者中，在不同剂量上观察到4例确认的PR，其中3例伴有ESR1突变，客观缓解率（ORR）为8%。在40例临床获益率（CBR）疗效可评估人群中，CBR率为25%。而且，SIM0270安全性良好，大多数治疗期不良事件（TEAEs）为1-2级。       SIM0235是一种针对TNFR2的人源化IgG1单克隆抗体，可阻断内源性肿瘤坏死因子 (TNF) 对 TNFR2 的活化，从而降低TNFR2引发的免疫抑制和肿瘤增生，增强抗肿瘤免疫应答。此外，该药还能通过抗体依赖性细胞毒性 (ADCC) 和抗体依赖性细胞吞噬作用 (ADCP)，杀伤表达TNFR2的免疫抑制细胞，包括调节型T细胞和髓系来源的免疫抑制细胞。2023年3月，先声药业与默沙东达成临床开发合作，探索SIM0235联合PD-1抗体KEYTRUDA®️治疗晚期实体瘤及皮肤T细胞淋巴瘤（CTCL）的潜力。在临床前研究中，已观察到SIM0235与KEYTRUDA联用具有良好的作用，有望为肿瘤患者带来临床获益。       SIM0272是一款合成致死药物，作用于蛋白质精氨酸甲基转移酶5（PRMT5）。药代动力学研究显示，SIM0272倾向于分布在肿瘤内，肿瘤内药物浓度与血浆药物浓度比值是其他在研PRMT5抑制剂的10倍左右。而且，SIM0272在体外展现出对多种血液瘤和实体瘤细胞的增殖抑制活性，且单药能显著抑制多个小鼠CDX模型中的肿瘤生长。2022年3月，该药在国内获批临床，拟用于治疗晚期恶性肿瘤。       SIM0237是先声再明蛋白质工程技术平台自主开发的一种抗PD-L1单抗与减活IL-15/IL-15Rα sushi融合蛋白，可通过结合PD-L1，阻断PD-1/PD-L1免疫抑制通路，同时通过IL-15激活免疫系统，从而实现解除免疫抑制和激活免疫系统的双重协同效应，发挥抗肿瘤作用。临床前研究显示，SIM0237在小鼠肿瘤模型中药效优于PD-L1单药和IL-15单药，有较高的临床开发潜力。       SIM0348是一种基于IgG1的人源化TIGIT/PVRIG双特异性抗体。临床前数据显示，SIM0348能有效促进NK细胞对人结直肠癌细胞和人血液白血病细胞的杀伤，同时还能显著增强抗原特异性CD8+T细胞分泌IFN-γ因子，效果优于PVRIG单抗和TIGIT单抗联用，且与抗PD-L1抗体联合显示出了显著的联用效果，优于任一单药药效且优于三药联用。2023年3月，该药治疗晚期实体瘤的1期临床试验完成首例患者给药。       总结       肿瘤是全球最大药物市场，每个药企都期望从中分一杯羹，先声药业也不例外，在肿瘤领域布局广泛。目前，先声药业已有三款肿瘤药物获批上市，第四款肿瘤药物已申请上市，多款新靶点药物进入临床。期待先声药业肿瘤管线早日开花结果。      【智药研习社近期直播预告】来源：CPHI制药在线声明：本文仅代表作者观点，并不代表制药在线立场。本网站内容仅出于传递更多信息之目的。如需转载，请务必注明文章来源和作者。投稿邮箱：Kelly.Xiao@imsinoexpo.com▼更多制药资讯，请关注CPHI制药在线▼点击阅读原文，进入智药研习社~

HOLON, Israel, March 6, 2024 /PRNewswire/ -- Compugen Ltd. (Nasdaq: CGEN) (TASE: CGEN), a clinical-stage cancer immunotherapy company and a pioneer in computational target discovery, today announced that it will present data from its differentiated immuno-oncology preclinical and clinical pipeline, in two poster presentations at the American Association for Cancer Research (AACR) annual meeting on April 5-11, 2024, in San Diego, California. "It is exciting that the progress we have made to potentially address immunotherapy resistance from diverse angles will be reflected at AACR this year," said Anat Cohen-Dayag, Ph.D., President, and CEO of Compugen. "While PVRIG and TIGIT are novel targets discovered with our computational discovery platform, more recently, we have also discovered a unique and differentiated way to target a known biological pathway, the IL-18 binding protein pathway." Eran Ophir, Ph.D., Chief Scientific Officer at Compugen, added, "At ACCR we will present data supporting the unique biology of PVRIG suggesting its role in sensitizing tumors to other immune checkpoints TIGIT and PD-(L)1. In addition, in a second presentation we will present data supporting the therapeutic potential of our high affinity, potential first-in-class, anti-IL-18 binding protein antibody, COM503, showing its activity is localized to the tumor microenvironment with the potential advantage of a wider therapeutic window than systemically delivered cytokines." Poster details: Session Date and Time: Tuesday, April 9, 2024, 9:00 AM - 12:30 PM PST Session Category: Immunology Session Title: Immune Modulation with Cytokines Poster Title: Unleashing natural IL-18 activity using an anti-IL-18BP blocker antibody induces potent immune stimulation and anti-tumor effects Published Abstract Number: 4072 Session Date and Time: Wednesday, April 10, 2024, 9:00 AM - 12:30 PM PST Session Category: Clinical Research Session Title: Immune Checkpoint Inhibitor Therapy Poster Title: PVRIG is uniquely expressed in tumor dendritic cells-rich niches on stem-like memory T cells and its blockade may induce immune infiltration and activation in non-inflamed tumor Published Abstract Number: 7533 The abstracts are available on Compugen's website at . The data will be published in the online Proceedings supplement to the AACR journal Cancer Research prior to the meeting on Friday, March 22, 2024. About Compugen Compugen is a clinical-stage therapeutic discovery and development company utilizing its broadly applicable predictive computational discovery capabilities to identify new drug targets and biological pathways for developing cancer immunotherapies. Compugen has developed two proprietary product candidates: COM701, a potential first-in-class anti-PVRIG antibody and COM902, a potential best-in-class antibody targeting TIGIT for the treatment of solid tumors. Compugen also has a clinical stage partnered program, rilvegostomig (previously AZD2936), a PD-1/TIGIT bispecific antibody where the TIGIT component is derived from Compugen's clinical stage anti-TIGIT antibody, COM902, in Phase 3 development by AstraZeneca through a license agreement for the development of bispecific and multispecific antibodies. In addition, the Company's therapeutic pipeline of early-stage immuno-oncology programs consists of programs aiming to address various mechanisms of immune resistance, of which the most advanced program, COM503, is in IND enabling studies is licenced to Gilead. COM503 is a potential first-in-class, high affinity antibody which blocks the interaction between IL-18 binding protein and IL-18, thereby freeing natural IL-18 in the tumor microenvironment to inhibit cancer growth. Compugen is headquartered in Israel, with offices in San Francisco, CA. Compugen's shares are listed on Nasdaq and the Tel Aviv Stock Exchange under the ticker symbol CGEN. Forward-Looking Statement This press release contains "forward-looking statements" within the meaning of the Securities Act of 1933 and the Securities Exchange Act of 1934, as amended, and the safe-harbor provisions of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements are based on the current beliefs, expectations, and assumptions of Compugen. Forward-looking statements can be identified using terminology such as "will," "may," "expects," "anticipates," "believes," "potential," "plan," "goal," "estimate," "likely," "should," "confident," and "intends," and similar expressions that are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. Forward-looking statements include, but are not limited to, statements relating to our expectation to present data from our differentiated immuno-oncology preclinical and clinical pipeline, in two poster presentations at the AACR annual meeting in 2024. These forward-looking statements involve known and unknown risks and uncertainties that may cause the actual results, performance, or achievements of Compugen to be materially different from any future results, performance or achievements expressed or implied by such forward-looking statements. Among these risks: Compugen's business model is substantially dependent on entering into collaboration agreements with third parties and Compugen may not be successful in generating adequate revenues or commercializing aspects of its business model; Compugen's approach to the discovery of therapeutic products is based on its proprietary computational target discovery infrastructure, which is unproven clinically; Compugen does not know whether it will be able to discover and develop additional potential product candidates or products of commercial value; and the general market, political and economic conditions in the countries in which Compugen operates, including Israel; and the effect of the evolving nature of the recent war in Gaza between Israel and Hamas. These risks and other risks are more fully discussed in the "Risk Factors" section of Compugen's most recent Annual Report on Form 20-F as filed with the Securities and Exchange Commission (SEC) as well as other documents that may be subsequently filed by Compugen from time to time with the SEC. In addition, any forward-looking statements represent Compugen's views only as of the date of this release and should not be relied upon as representing its views as of any subsequent date. Compugen does not assume any obligation to update any forward-looking statements unless required by law. Company contact: Yvonne Naughton, Ph.D. Head of Investor Relations and Corporate Communications Email: [email protected] Tel: +1 (628) 241-0071 SOURCE Compugen Ltd.

Partnership with Gilead on preclinical immuno-oncology program further validates Compugen's computational discovery, research, and development capabilities Catalyst rich 2024 expected with multiple data readouts and updates planned from Compugen's diversified portfolio Solid balance sheet with extended cash runway expected to fund operations into 2027 HOLON, Israel, March 5, 2024 /PRNewswire/ -- Compugen Ltd. (NASDAQ: CGEN) (TASE: CGEN) a clinical-stage cancer immunotherapy company and a pioneer in computational target discovery, today reported financial results for the fourth quarter and full year 2023 and provided a corporate update. "Our accomplishments in 2023 position us well for an exciting future," said Anat Cohen-Dayag, Ph.D., President, and CEO of Compugen. "We advance into an expected catalyst rich 2024, with a solid balance sheet, an expected extended cash runway into 2027 and validating partnerships. We believe we have the tools in place to accelerate value creation through advancement of our diversified pipeline portfolio along with our computational discovery platform which is the engine powering our competitive advantage." Dr. Cohen-Dayag added, "Compugen made significant progress in 2023, including a license agreement with Gilead Sciences for our preclinical potential first-in-class, antibody program against IL-18 binding protein, COM503. The deal, including an upfront payment of $60 million and an additional $30 million near term milestone payment, reflects on our computational discovery, research, and development capabilities. Compugen is expected to lead the Phase 1 development of COM503 and is on track for IND submission in the second half of 2024 with subsequent initiation of the Phase 1 study following IND clearance. In 2023 we also progressed our novel COM701 triple combination strategy with the initiation of two proof-of concept studies, in MSS CRC including patients with liver metastases, and in platinum resistant ovarian cancer and we expect to report data from these studies in the first half of 2024 and the fourth quarter of 2024, respectively. While these are particularly challenging indications to treat having historically failed to respond to immunotherapy, representing a high bar for success, we previously presented encouraging clinical data, supported by immune activation suggesting that the unique biology of PVRIG enables anti-PD-1 activity in these challenging indications. The goal of these studies is to further substantiate our clinical findings including our initial biomarker results, to potentially enable us to move forward with a biomarker enriched development strategy." Dr. Cohen-Dayag continued, "In 2023, our partner AstraZeneca continued to make progress advancing rilvegostomig, a PD-1/TIGIT bispecific antibody, the TIGIT component of which is derived from our COM902, into Phase 3 development in biliary tract cancer. AstraZeneca is also advancing rilvegostomig across multiple other indications and combinations and expects data from two of these Phase 2 trials, in the second half of 2024. This partnership provides further validation to our potential best-in-class anti-TIGIT, COM902, and the extensive clinical program being run by AstraZeneca increases our opportunity for obtaining additional non-dilutive financing through expected future milestone payments and royalties." Upcoming Expected Milestones: COM701 +COM902 + pembrolizumab proof-of-concept studies Microsatellite stable colorectal cancer - data in the first half of 2024 Platinum resistant ovarian cancer - on track to complete enrolment of at least 20 patients in the first quarter of 2024, and data in the fourth quarter of 2024 COM503 (Licenced to Gilead, Compugen responsible through Phase 1 development) IND submission in the second half of 2024 with subsequent initiation of the Phase 1 study following IND clearance Rilvegostomig (AstraZeneca's PD-1/TIGIT bispecific, TIGIT component derived from COM902) Data in the second half of 2024 from Phase 1/2 ARTEMIDE-01 trial in advanced/metastatic NSCLC and Phase 2b GEMINI-HBP trial in hepatobiliary cancer Fourth Quarter and Full Year 2023 Financial Highlights Cash: As of December 31, 2023, Compugen had approximately $51.1 million in cash, cash equivalents, restricted cash, and cash investments, compared with approximately $83.7 million as of December 31, 2022. The cash balance at the end of 2023 does not include the receipt of the upfront payment of $60 million from Gilead for the licensing of COM503 and the $10 million milestone payment from AstraZeneca on dosing of the first patient in the rilvegostomig Phase 3 trial in biliary tract cancer. Compugen expects to receive from Gilead an additional $30 million milestone payment on COM503 IND clearance in 2024. All payments from Gilead are subject to a 15% withholding tax. During the three months ended December 31, 2023, the Company sold approximately 0.9 million ordinary shares under it's at the market offering (ATM) facility pursuant to a sales agreement entered into with Leerink Partners on January 31, 2023, for aggregate gross proceeds of approximately $1.9 million. Subsequent to the financial results for the year ended December 31, 2023, a total of approximately 0.3 million shares were sold through the Company's ATM facility contributing gross proceeds of approximately $0.6 million. Compugen expects that its cash and cash-related balances will be sufficient to fund its operating plans into 2027. The Company has no debt. Revenues: Compugen reported approximately $33.5 million in revenues for the fourth quarter and for the year ended December 31, 2023, compared to $7.5 million revenues for each of the comparable periods in 2022. The 2023 recognized revenues include the portion of the upfront payment from the license agreement with Gilead allocated to the license and the $10 million clinical milestone payment from AstraZeneca. R&D expenses for the fourth quarter and year ended December 31, 2023, increased to approximately $10.9 million, and $34.5 million, respectively, compared with $7.3 million and $30.6 million for the comparable periods in 2022, respectively. The increase in 2023 is mainly due to lower amortization of the deferred participation in R&D expenses following the termination of the agreement with Bristol Myers Squibb, offset by decrease in headcount related expenses. Research and development expenses, as a percentage of total operating expenses, were 78% in 2023 compared to 73% in 2022. G&A expenses for the fourth quarter and year ended December 31, 2023, were $2.5 million and $9.7 million, respectively, compared with approximately $2.5 million and approximately $10.3 million for the comparable periods in 2022, respectively. Net Income / Loss: During the fourth quarter of 2023, Compugen reported a net profit of $9.7 million, or 11 cents per basic and diluted share, compared to a net loss of $3.1 million, or 4 cents per basic and diluted share in the comparable period of 2022. Net loss for the year ended December 31, 2023, was $18.8 million, or 21 cents per basic and diluted share, compared with a net loss of $33.7 million, or 39 cents per basic and diluted share in the comparable period in 2022. Full financial tables are included below. Conference Call and Webcast Information The Company will hold a conference call today, March 5, 2024, at 8:30 AM ET to review its fourth quarter and full year 2023 results. To access the conference call by telephone, please dial 1-866-744-5399 from the United States, or +972-3-918-0644 internationally. The call will also be available via live webcast through Compugen's website, located at the following link. Following the live audio webcast, a replay will be available on the Company's website. About Compugen Compugen is a clinical-stage therapeutic discovery and development company utilizing its broadly applicable predictive computational discovery capabilities to identify new drug targets and biological pathways for developing cancer immunotherapies. Compugen has developed two proprietary product candidates: COM701, a potential first-in-class anti-PVRIG antibody and COM902, a potential best-in-class antibody targeting TIGIT for the treatment of solid tumors. Compugen also has a clinical stage partnered program, rilvegostomig (previously AZD2936), a PD-1/TIGIT bispecific antibody where the TIGIT component is derived from Compugen's clinical stage anti-TIGIT antibody, COM902, in Phase 3 development by AstraZeneca through a license agreement for the development of bispecific and multispecific antibodies. In addition, Compugen's therapeutic pipeline of early-stage immuno-oncology programs consists of programs aiming to address various mechanisms of immune resistance, of which the most advanced program, in IND enabling studies is COM503, which is licensed to Gilead. COM503 is a potential first-in-class, high affinity antibody which blocks the interaction between IL-18 binding protein and IL-18, thereby freeing natural IL-18 in the tumor microenvironment to inhibit cancer growth. Compugen is headquartered in Israel, with offices in San Francisco, CA. Compugen's shares are listed on Nasdaq and the Tel Aviv Stock Exchange under the ticker symbol CGEN. Forward-Looking Statement This press release contains "forward-looking statements" within the meaning of the Securities Act of 1933 and the Securities Exchange Act of 1934, as amended, and the safe-harbor provisions of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements are based on the current beliefs, expectations, and assumptions of Compugen. Forward-looking statements can be identified using terminology such as "will," "may," "expects," "anticipates," "believes," "potential," "plan," "goal," "estimate," "likely," "should," "confident," and "intends," and similar expressions that are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. Forward-looking statements include, but are not limited to, statement regarding our expectations regarding IND clearance for COM503, including the timing thereof, and similar statements regarding the initiation, and timing of the Phase 1 study for COM503, statements regarding our expectation that 2024 will be catalyst rich with multiple data readouts and updates planned for Compugen's diversified portfolio, statements suggesting that the unique biology of PVRIG enables anti-PD-1 activity in MSS CRC including patients with liver metastases, and in platinum resistant ovarian cancer, statements regarding our ability to move forward with an enriched development strategy and statements to the effect that our cash and cash-related balances will be sufficient to fund our operating plans into 2027. These forward-looking statements involve known and unknown risks and uncertainties that may cause the actual results, performance, or achievements of Compugen to be materially different from any future results, performance or achievements expressed or implied by such forward-looking statements. Among these risks: the clinical trials of any product candidates that Compugen, or any current or future collaborators, may develop may fail to satisfactorily demonstrate safety and efficacy to the FDA, and Compugen, or any collaborators, may incur additional costs or experience delays in completing, or ultimately be unable to complete, the development and commercialization of these product candidates; Compugen's business model is substantially dependent on entering into collaboration agreements with third parties and Compugen may not be successful in generating adequate revenues or commercializing aspects of its business model; Compugen's approach to the discovery of therapeutic products is based on its proprietary computational target discovery infrastructure, which is unproven clinically; general market, political and economic conditions in the countries in which Compugen operates, including Israel; the effect of the evolving nature of the recent war in Gaza; and Compugen does not know whether it will be able to discover and develop additional potential product candidates or products of commercial value. These risks and other risks are more fully discussed in the "Risk Factors" section of Compugen's most recent Annual Report on Form 20-F as filed with the Securities and Exchange Commission (SEC) as well as other documents that may be subsequently filed by Compugen from time to time with the SEC. In addition, any forward-looking statements represent Compugen's views only as of the date of this release and should not be relied upon as representing its views as of any subsequent date. Compugen does not assume any obligation to update any forward-looking statements unless required by law. Company contact: Yvonne Naughton, Ph.D. Head of Investor Relations and Corporate Communications Email: ir@cgen.com Tel: +1 (628) 241-0071 SOURCE Compugen Ltd.