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Anixa Biosciences Treats Sixth Patient in Its Ovarian Cancer CAR-T Clinical Trial

Anixa Biosciences Treats Sixth Patient in Its Ovarian Cancer CAR-T Clinical Trial

anixa biosciences在其卵巢癌car-t臨床試驗中治療了第六名患者。
Anixa Biosciences ·  06/24 00:00

This patient is expected to be the final patient in the second dosage cohort of the trial

預計該患者將成爲該試驗第二劑量隊列中的最後一名患者

SAN JOSE, Calif., June 24, 2024 /PRNewswire/ -- Anixa Biosciences, Inc. ("Anixa" or the "Company") (NASDAQ: ANIX), a biotechnology company focused on the treatment and prevention of cancer, today announced that it has treated the sixth patient in the ongoing Phase 1 clinical trial of its novel chimeric antigen receptor T-cell (CAR-T) therapy for ovarian cancer. This patient is expected to be the last patient in the second dosage cohort. If there continue to be no adverse effects experienced by the second cohort participants, enrollment of the third dosage cohort may commence within the next month. The study is being conducted through a research partnership with Moffitt Cancer Center.

加利福尼亞州聖何塞,2024 年 6 月 24 日 /PRNewswire/-- Anixa Biosciences, Inc (“Anixa” 或 “公司”)(納斯達克股票代碼:ANIX)是一家專注於癌症治療和預防的生物技術公司,今天宣佈,在正在進行的卵巢癌新型嵌合抗原受體T細胞(CAR-T)療法的1期臨床試驗中,它已經治療了第六名患者。預計該患者將成爲第二劑量隊列中的最後一位患者。如果第二組參與者仍然沒有出現不良反應,則第三劑量隊列的註冊可能在下個月內開始。該研究是通過與莫菲特癌症中心的研究合作進行的。

Anixa's FSHR-mediated CAR-T technology, also known as chimeric endocrine receptor T-cell (CER-T), differs from traditional CAR-T therapy by targeting the follicle-stimulating hormone receptor (FSHR), which research indicates is exclusively expressed on ovarian cells, including the vasculature of tumors. The first-in-human trial (NCT05316129) is enrolling female adult patients with recurrent/progressing ovarian cancer who have progressed on at least two prior therapies. The study is designed to evaluate safety and identify the maximum tolerated dose, while monitoring efficacy.

Anixa的FSHR介導的CAR-T技術,也稱爲嵌合內分泌受體T細胞(CER-T),與傳統的CAR-T療法的不同之處在於靶向卵泡刺激激素受體(FSHR),研究表明卵泡刺激素受體(FSHR)僅在卵巢細胞上表達,包括腫瘤的血管系統。首次人體試驗 (NCT05316129)正在招收在先前至少兩種療法中取得進展的復發/進展性卵巢癌的女性成年患者。該研究旨在評估安全性並確定最大耐受劑量,同時監測療效。

Safety was previously confirmed in the first three-patient cohort. The fourth through sixth patients, enrolled in the second cohort of the Phase 1 clinical trial, received triple the dose of CAR-T cells compared with the dose of the first cohort, with no dose-limiting toxicities observed.

此前在前三名患者中證實了安全性。加入1期臨床試驗第二組的第四至第六名患者接受的CAR-T細胞劑量是第一隊列劑量的三倍,未觀察到劑量限制毒性。

Following the requisite wait time, of one month after dosing, enabling confirmation that it is safe to escalate, the trial will immediately begin enrolling patients in the third dose cohort, which will be at a ten times higher dose than the initial dosage.

在給藥後一個月的必要等待時間之後,該試驗將立即開始將患者納入第三劑隊列,其劑量將比初始劑量高十倍。

Dr. Amit Kumar, Chairman and CEO of Anixa Biosciences, stated, "We are highly encouraged by the favorable safety profile observed thus far in both the first and second patient cohorts, and are eager to evaluate a higher dose in the next cohort. We are particularly encouraged by a notable response in one of the patients in the first cohort, even though the dosage was considered a subtherapeutic level. Our aim is to maintain a positive safety profile as we escalate dosing, with the goal of demonstrating additional objective evidence of efficacy. Unlike conventional CAR-T cell therapies, which have achieved amazing results in various hematological cancers, they have not been effective in solid tumors. In contrast, we believe Anixa's novel technology has the potential to make CAR-T effective in ovarian cancer and perhaps across multiple solid tumor types. Our unique and highly targeted CER-T approach targets the FSHR, which is exclusively expressed on ovarian cells. A potential dual mechanism of action is operating with our therapy targeting tumor vasculature by starving or shrinking the tumor from the inside out, as well as direct targeting of ovarian cells."

Anixa Biosciences董事長兼首席執行官阿米特·庫馬爾博士表示:“迄今爲止,在第一和第二組患者中觀察到的良好安全狀況令我們深受鼓舞,並渴望在下一組患者中評估更高的劑量。特別令我們感到鼓舞的是,儘管劑量被認爲是亞於治療水平,但第一組患者還是出現了顯著的反應。我們的目標是在增加劑量時保持積極的安全性,目的是證明更多的療效客觀證據。與在各種血液系統癌症中取得驚人效果的傳統CAR-T細胞療法不同,它們對實體瘤並不有效。相比之下,我們認爲Anixa的新技術有可能使CAR-T對卵巢癌有效,並可能對多種實體瘤類型有效。我們獨特且具有高度針對性的CER-T方法靶向FSHR,FSHR僅在卵巢細胞上表達。一種潛在的雙重作用機制是,我們的療法以腫瘤血管系統爲目標,從內而外使腫瘤餓死或縮小,以及直接靶向卵巢細胞。”

Dr. Kumar continued, "We believe that intraperitoneal (IP) delivery may also be a significant advantage of our therapy, as it allows direct trafficking of the CAR-T cells to the tumor sites, which helps to minimize side effects such as cytokine release syndrome (CRS). We believe this method of delivery not only enhances the targeting of the tumor but also improves the overall safety profile of the treatment. We expect that IP delivery may enable us to use dosages that are much higher than possible with intravenous delivery."

庫馬爾博士繼續說:“我們認爲,腹膜內注射(IP)也可能是我們療法的顯著優勢,因爲它允許將CAR-T細胞直接運送到腫瘤部位,這有助於最大限度地減少細胞因子釋放綜合徵(CRS)等副作用。我們認爲,這種給藥方法不僅可以增強腫瘤的靶向,還可以提高治療的整體安全性。我們預計,IP輸送可能使我們能夠使用比靜脈注射高得多的劑量。”

About Anixa Biosciences, Inc.

關於 Anixa Biosciences, Inc.

Anixa is a clinical-stage biotechnology company focused on the treatment and prevention of cancer. Anixa's therapeutic portfolio consists of an ovarian cancer immunotherapy program being developed in collaboration with Moffitt Cancer Center, which uses a novel type of CAR-T, known as chimeric endocrine receptor T-cell (CER-T) technology. The Company's vaccine portfolio includes vaccines being developed in collaboration with Cleveland Clinic to prevent breast cancer – specifically triple negative breast cancer (TNBC), the most lethal form of the disease – and ovarian cancer, as well as additional cancer vaccines to address many intractable cancers, including high incidence malignancies in lung, colon, and prostate. These vaccine technologies focus on immunizing against "retired" proteins that have been found to be expressed in certain forms of cancer. Anixa's unique business model of partnering with world-renowned research institutions on all stages of development allows the Company to continually examine emerging technologies in complementary fields for further development and commercialization. To learn more, visit www.anixa.com or follow Anixa on Twitter, LinkedIn, Facebook and YouTube.

Anixa是一家臨床階段的生物技術公司,專注於癌症的治療和預防。Anixa的治療產品組合包括與莫菲特癌症中心合作開發的卵巢癌免疫療法計劃,該計劃使用一種新型的CAR-T,即嵌合內分泌受體T細胞(CER-T)技術。該公司的疫苗產品組合包括與克利夫蘭診所合作開發的預防乳腺癌(特別是三陰性乳腺癌(TNBC),該疾病中最致命的形式)和卵巢癌的疫苗,以及其他用於治療許多難治癌症的癌症疫苗,包括肺部、結腸和前列腺的高發惡性腫瘤。這些疫苗技術側重於對已發現可在某些形式的癌症中表達的 “退役” 蛋白進行免疫接種。Anixa在各個開發階段與世界知名研究機構合作的獨特商業模式使公司能夠不斷研究互補領域的新興技術,以進一步開發和商業化。要了解更多信息,請訪問 www.anixa.com 或者繼續關注 Anixa 推特領英Facebook優酷

Forward-Looking Statements

前瞻性陳述

Statements that are not historical fact may be considered forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements are not statements of historical facts, but rather reflect Anixa's current expectations concerning future events and results. We generally use the words "believes," "expects," "intends," "plans," "anticipates," "likely," "will" and similar expressions to identify forward-looking statements. Such forward-looking statements, including those concerning our expectations, involve risks, uncertainties and other factors, some of which are beyond our control, which may cause our actual results, performance or achievements, or industry results, to be materially different from any future results, performance, or achievements expressed or implied by such forward-looking statements. These risks, uncertainties and factors include, but are not limited to, those factors set forth in "Item 1A - Risk Factors" and other sections of our most recent Annual Report on Form 10-K as well as in our Quarterly Reports on Form 10-Q and Current Reports on Form 8-K. We undertake no obligation to publicly update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as required by law. You are cautioned not to unduly rely on such forward-looking statements when evaluating the information presented in this press release.

根據1995年《私人證券訴訟改革法》,非歷史事實的陳述可以被視爲前瞻性陳述。前瞻性陳述不是對歷史事實的陳述,而是反映了Anixa當前對未來事件和結果的預期。我們通常使用 “相信”、“期望”、“打算”、“計劃”、“預期”、“可能”、“將” 等詞語以及類似的表述來識別前瞻性陳述。此類前瞻性陳述,包括與我們的預期有關的陳述,涉及風險、不確定性和其他因素,其中一些因素是我們無法控制的,這可能導致我們的實際業績、業績或成就或行業業績與此類前瞻性陳述所表達或暗示的任何未來業績、業績或成就存在重大差異。這些風險、不確定性和因素包括但不限於 “項目1A——風險因素” 和我們最新的10-K表年度報告以及我們的10-Q表季度報告和8-K表最新報告的其他部分中列出的因素。除非法律要求,否則我們沒有義務公開更新或修改任何前瞻性陳述,無論是由於新信息、未來事件還是其他原因。提醒您在評估本新聞稿中提供的信息時不要過度依賴此類前瞻性陳述。

Contact:
Mike Catelani
President, COO & CFO
mcatelani@anixa.com
408-708-9808

聯繫人:
邁克·卡特拉尼
總裁、首席運營官兼首席財務官
mcatelani@anixa.com
408-708-9808

SOURCE  Anixa Biosciences, Inc.

來源 Anixa Biosciences, Inc.

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