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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位患者。
Anixa Biosciences ·  06/24 12:00

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

該患者預計將成爲試驗第二劑量隊列的最後一個患者。

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 /美通社/ -- 生物技術公司anixa生物科學公司(Anixa)(納斯達克:ANIX)一家致力於癌症治療和預防的生物技術公司anixa生物科學公司(Anixa)(納斯達克:ANIX),今天宣佈已爲正在進行的卵巢癌第一期臨床試驗中,使用其新型嵌合抗原受體T細胞(CAR-T)治療卵巢癌的受試者中的第六名患者提供治療。這位患者預計將是第二劑量隊列中的最後一位。如果第二隊列參與者繼續沒有經歷不良反應,則第三劑量隊列的入組可能會在下個月開始。這項研究是通過與莫菲特癌症中心的合作進行的研究合作進行的。

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),通過針對促卵泡素受體(FSHR),與傳統的CAR-T療法不同,研究表明該受體只在包括腫瘤血管在內的卵巢細胞上表達。正在進行的第一項試驗(NCT05316129)招募了復發/進展的卵巢癌女性成人患者,這些患者已在至少兩種先前的治療方案上發展。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。招募女性成年復發/進展的卵巢癌患者,這些患者已經接受過至少兩種先前的治療。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.

前三位患者隊列的安全性已經得到確認。第一階段臨床試驗的第4至第6位患者接受的CAR-T細胞劑量比第一隊列的劑量高三倍,未觀察到劑量限制性毒性。

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.

在劑量達到一個月的必需等待時間之後,以確認其安全性可以升級,該試驗將立即開始招募第三劑量隊列的患者,該劑量將是起始劑量的10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生物科學公司(Anixa Biosciences)的董事長兼首席執行官Amit Kumar博士表示:“我們非常鼓舞人心,迄今爲止在第一和第二批患者隊列中觀察到了良好的安全性評價,我們渴望在下一個隊列中評估更高的劑量。我們特別注意到,在第一批患者中,即使劑量被認爲是亞治療水平,其中一位患者也出現了明顯的反應。我們的目標是在不斷升級劑量的同時保持積極的安全性評價,以展示額外的客觀療效證據。與在各種血液腫瘤中取得驚人成果的傳統CAR-T細胞療法不同,它們在實體腫瘤中並不有效。相反,我們相信Anixa的新技術有可能使CAR-T在卵巢癌中有效,並且在多種實體腫瘤類型中具有潛在的作用。我們獨特且高度定向的CER-T方法針對FSHR,該受體僅在卵巢細胞上表達。該療法通過使腫瘤從內部飢餓或萎縮來靶向腫瘤血管,以及直接靶向卵巢細胞,可能具有潛在的雙重機制作用。”

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."

Kumar博士繼續說:“我們相信腹膜內(IP)輸送也可能是我們的治療方法的一個重要優勢,因爲它允許CAR-T細胞直接傳輸到腫瘤部位,從而有助於最小化細胞因子釋放綜合徵(CRS)等副作用。我們相信,這種傳輸方法不僅增強了對腫瘤的靶向作用,還提高了整體治療的安全性。我們預計IP輸送可能使我們使用的劑量比靜脈輸送可能更高。”

About Anixa Biosciences, Inc.

Anixa生物科學公司(Anixa Biosciences)

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是一家專注於腫瘤治療和預防的臨床階段的生物技術公司。 Anixa的治療組合包括與Moffitt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,稱爲嵌合內分泌受體T細胞(CER-T)技術。該公司疫苗組合包括與Cleveland Clinic合作開發的疫苗,以預防乳腺癌(特別是三陰性乳腺癌,該疾病是最致命的形式之一)和卵巢癌,以及額外的癌症疫苗,用於治療包括肺部,結腸和前列腺等高發惡性腫瘤在內的許多難治癌症。這些疫苗技術專注於免疫對某些形式的癌症表達的“退役”蛋白質。Anixa與世界知名的研究機構的合作模式允許公司在發展和商業化期間不斷檢查互補領域的新興技術。要了解更多信息,請訪問www.anixa.com或在 關於Anixa Biosciences,Inc. 或關注anixa。推特, LinkedIn, Facebook和頁面。YouTube.

Forward-Looking Statements

前瞻性聲明

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.

本新聞稿中不是歷史事實的聲明可被視爲美國《1995年私人證券訴訟改革法》中的前瞻性聲明。前瞻性聲明不是歷史事實的陳述,而是反映Anixa有關未來事件和結果的當前期望。我們通常使用“相信”,“預計”,“計劃”,“打算”,“預測”,“可能”,“將”等類似詞語來識別前瞻性聲明。這樣的前瞻性聲明,包括關於我們的預期,涉及風險,不確定性和其他因素的聲明,其中一些因素超出我們的控制,這可能導致我們的實際結果,績效或成就或行業成果與任何未來結果,績效或成就所反映的相比有實質性區別。我們的前瞻性聲明,包括有關我們的預期的聲明,涉及風險,不確定性和其他因素,其中一些因素在我們最近的年度報告的“項目1A - 風險因素”和其他章節,包括在我們的季度報告中提到 10-Q和當前的8-K報告。我們承諾不公開更新或修訂任何前瞻性聲明,無論是因爲獲得新信息,未來事件或其他原因,除非法律要求。在評估本新聞稿中所呈現的信息時,如果評估此類前瞻性聲明,應謹慎。

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

聯繫方式:
Mike Catelani
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。

譯文內容由第三人軟體翻譯。


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