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Kiromic BioPharma Reports Favorable Early Safety and Tolerability Data From First Patient Enrolled in the Phase 1 Deltacel-01 Clinical Trial

Kiromic BioPharma Reports Favorable Early Safety and Tolerability Data From First Patient Enrolled in the Phase 1 Deltacel-01 Clinical Trial

Kiromic BioPharma報告了參加1期Deltacel-01臨床試驗的首位患者的良好早期安全性和耐受性數據
Kiromic BioPharma ·  01/05 13:00

Company Executives Available to Meet with Investment Professionals January 8-10 in San Francisco

公司高管將於1月8日至10日在舊金山與投資專業人士會面

HOUSTON--(BUSINESS WIRE)--Jan. 5, 2024-- Kiromic BioPharma, Inc. (OTCQB: KRBP) ("Kiromic" or the "Company"), a clinical-stage, fully-integrated biotherapeutics company using its proprietary DIAMOND artificial intelligence and data mining platform to develop cell therapies with a focus on immuno-oncology, reports favorable safety and tolerability from the first patient 23 days after Deltacel infusion in the Phase 1 clinical trial for treatment of stage 4 metastatic non-small cell lung cancer (NSCLC) at Beverly Hills Cancer Center, located in Beverly Hills, California, USA. Specifically, laboratory test results and observations by clinical staff identified no adverse events and confirmed that Deltacel is being well tolerated with initial safety profile. Continued monitoring of safety and tolerability will provide more insights as the trial enrolls additional patients.

休斯頓--(美國商業資訊)--2024年1月5日-- Kiromic BioPharma, Inc.(場外交易代碼:KRBP)(“Kiromic” 或 “公司”),一家處於臨床階段、完全整合的生物療法公司,使用其專有的 DIAMOND 開發以免疫腫瘤學爲重點的細胞療法的人工智能和數據挖掘平台報告稱,在美國加利福尼亞州比佛利山莊的比佛利山莊癌症中心進行的治療4期轉移性非小細胞肺癌(NSCLC)的1期臨床試驗中,在Deltacel輸液23天后,首位患者具有良好的安全性和耐受性。具體而言,實驗室測試結果和臨床工作人員的觀察沒有發現任何不良事件,並證實了Deltacel的耐受性良好,初步的安全性如何。隨着試驗招收更多患者,持續監測安全性和耐受性將提供更多見解。

Kiromic expects to report preliminary efficacy results from this patient by the end of January 2024. Two more patients are expected to be enrolled between January and February 2024.

Kiromic預計將在2024年1月底之前報告該患者的初步療效結果。預計將在2024年1月至2月期間再入組兩名患者。

"Our first-in-human clinical trial of Deltacel is proceeding very well and on plan," said Pietro Bersani, Chief Executive Officer of Kiromic. "With no adverse events observed during the first 23 days post-treatment, we have strong indication that Deltacel is well tolerated. We look forward to discussing updates with members of the investment community during our meetings next week in San Francisco, concurrent with the 42nd Annual J.P. Morgan Healthcare Conference."

Kiromic首席執行官彼得羅·貝爾薩尼表示:“我們對Deltacel的首次人體臨床試驗進展順利,正在按計劃進行。”“由於在治療後的前23天內沒有觀察到任何不良事件,我們有強烈的跡象表明Deltacel的耐受性良好。我們期待在下週在舊金山舉行的會議上與投資界成員討論最新情況,同時舉行42次會議 摩根大通年度醫療保健會議。”

Investment professionals interested in meeting with Mr. Bersani, Chief Financial Officer Brian Hungerford and Chief Scientific Officer Dr. Leonardo Mirandola at LHA's offsite event being held January 8-10 should contact Tirth Patel at tpatel@lhai.com.

有興趣在1月8日至10日舉行的LHA場外活動上與伯薩尼先生、首席財務官布萊恩·亨格福德和首席科學官萊昂納多·米蘭多拉博士會面的投資專業人士應通過以下方式與Tirth Patel聯繫 tpatel@lhai.com

"We are very pleased to see favorable initial safety and tolerability data from the first patient treated in our Deltacel-01 study," said Dr. Afshin Eli Gabayan, Medical Oncologist, Medical Director, and Principal Investigator at Beverly Hills Cancer Center. "Seeing no adverse events reported 23 days after Deltacel infusion provides early validation that this novel cell therapy is well tolerated when combined with low dose radiation for lung cancer patients. We look forward to further evaluating optimal dose level, efficacy, and long-term safety outcomes as additional patients are enrolled and treated. If this promising initial data is replicated in more patients, Deltacel could become a new alternative treatment option for NSCLC patients."

比佛利山莊癌症中心腫瘤內科醫生、醫學董事兼首席研究員阿夫辛·埃利·加巴揚博士說:“我們很高興看到我們在Deltacel-01研究中首次接受治療的患者提供了良好的初步安全性和耐受性數據。”“在Deltacel輸注23天后沒有報告任何不良事件,這可以及早驗證這種新型細胞療法與低劑量輻射相結合對肺癌患者的耐受性良好。隨着更多患者的入組和治療,我們期待進一步評估最佳劑量水平、療效和長期安全結果。如果將這一令人鼓舞的初步數據複製到更多患者身上,Deltacel可能成爲非小細胞肺癌患者新的替代治療選擇。”

About Deltacel-01

關於 Deltacel-01

In Kiromic's open-label Phase 1 clinical trial, titled "Phase 1 Trial Evaluating the Safety and Tolerability of Gamma Delta T Cell Infusions in Combination With Low Dose Radiotherapy in Subjects With Stage 4 Metastatic Non-Small Cell Lung Cancer" (NCT06069570), patients with stage 4 NSCLC will receive two intravenous infusions of Deltacel with four courses of low-dose, localized radiation over a 10-day period. The primary objective of the study is to evaluate safety, while secondary ones include objective response, progression-free survival, overall survival, time to progression, time to treatment response and disease control rates.

在 Kiromic 的開放標籤 1 期臨床試驗中,名爲 “評估第 4 期轉移性非小細胞肺癌受試者的伽瑪三角洲T細胞輸液聯合低劑量放射治療的安全性和耐受性” 的1期臨床試驗(NCT06069570),4期非小細胞肺癌患者將在10天內接受兩次靜脈注射Deltacel和四個療程的低劑量局部放療。該研究的主要目標是評估安全性,而次要目標包括客觀反應、無進展存活率、總存活率、進展時間、治療反應時間和疾病控制率。

About Deltacel

關於 Deltacel

Deltacel (KB-GDT-01) is an investigational gamma delta T-cell (GDT) therapy currently in the Deltacel-01 Phase 1 trial for the treatment of NSCLC. An allogeneic product consisting of unmodified, donor-derived gamma delta T cells, Deltacel is the leading candidate in Kiromic's GDT platform. Deltacel is designed to exploit the natural potency of GDT cells to target solid cancers, with an initial focus on NSCLC, the most prevalent type of lung cancer and representing about 80% to 85% of lung cancer cases. Data from two preclinical studies demonstrated Deltacel's favorable safety and efficacy profile when it was combined with low-dose radiation.

Deltacel(KB-GDT-01)是一種正在研究的伽瑪三角洲T細胞(GDT)療法,目前正在進行用於治療非小細胞肺癌的Deltacel-01 1期試驗。Deltacel是一種由未改性、供體衍生的伽瑪三角洲T細胞組成的異基因產品,是Kiromic的GDT平台的主要候選產品。Deltacel旨在利用GDT細胞的自然效力靶向實體癌,最初的重點是非小細胞肺癌,這是最常見的肺癌類型,約佔肺癌病例的80%至85%。兩項臨床前研究的數據表明,Deltacel與低劑量輻射聯合使用時具有良好的安全性和有效性。

About Kiromic BioPharma

關於 Kiromic BioPharma

Kiromic BioPharma, Inc. is a clinical-stage, fully integrated biotherapeutics company using its proprietary DIAMOND artificial intelligence (AI) 2.0 target discovery engine to develop and commercialize cell therapies focusing on immuno-oncology. Kiromic is developing a multi-indication allogeneic cell therapy platform that exploits the natural potency of Gamma Delta T-cells to target solid tumors. Kiromic's DIAMONDAI is where data science meets target identification to dramatically compress the years and hundreds of millions of dollars required to develop a live drug. The Company maintains offices in Houston, Texas. To learn more, visit www.kiromic.com and connect with us on Twitter and LinkedIn.

Kiromic BioPharma, Inc. 是一家處於臨床階段、完全整合的生物療法公司,使用其專有的 DIAMOND 人工智能 (AI) 2.0 瞄準發現引擎,開發和商業化細胞以免疫腫瘤學爲重點的療法。Kiromic正在開發一種多適應症同種異體細胞治療平台,該平台利用Gamma Delta T細胞的天然效力來靶向實體瘤。Kiromic 的鑽石人工智能是數據科學與靶標識別相結合的地方,可以顯著縮短開發活體藥物所需的時間和數億美元。該公司在德克薩斯州休斯敦設有辦事處。要了解更多信息,請訪問 www.kiromic.com 然後通過以下方式聯繫我們 推特領英

About Beverly Hills Cancer Center

關於比佛利山莊癌症中心

As a private, academic, community-based cancer center, Beverly Hills Cancer Center not only provides the latest state-of-the-art cancer treatments all under one roof, but also provides leading clinical trials and research, attracting patients globally. By providing access to groundbreaking clinical trials, the Beverly Hills Cancer Center offers patients the opportunity to participate in the most advanced cancer treatments currently in development in the world. Beverly Hills Cancer Center is composed of an internationally recognized multidisciplinary medical team consisting of Medical Oncologists, Radiation Oncologists, Radiologists, Hematologists and Internists who provide exceptional patient care and support services including a robust and highly efficient team of clinical research professionals. More information is available on: www.BHCancerCenter.com.

作爲一家以社區爲基礎的私立學術癌症中心,比佛利山莊癌症中心不僅在一個屋檐下提供最新的最先進的癌症治療方法,而且還提供領先的臨床試驗和研究,吸引全球患者。通過提供獲得開創性臨床試驗的機會,比佛利山莊癌症中心爲患者提供了參與目前世界上正在開發的最先進的癌症治療的機會。比佛利山癌症中心由一支國際認可的多學科醫療團隊組成,包括腫瘤內科醫生、放射腫瘤學家、放射科醫生、血液學家和內科醫生,他們提供卓越的患者護理和支持服務,包括一支強大而高效的臨床研究專業人員團隊。更多信息可在以下網址獲得: www.bhcancerCenter.co

Forward-Looking Statements

前瞻性陳述

This press release contains forward-looking statements that involve substantial risks and uncertainties. Kiromic makes such forward-looking statements pursuant to the safe harbor provisions of the United States Private Securities Litigation Reform Act, Section 21E of the Securities Exchange Act of 1934, as amended, and other federal securities laws. All statements other than statements of historical facts are forward-looking statements. In some cases, you can identify forward-looking statements by terms such as: "will," "potential," "could," "can," "believe," "intends," "continue," "plans," "expects," "anticipates," "estimates," "may," or the negative of these terms or other comparable terminology. These forward-looking statements include, but are not limited to, statements regarding: Kiromic's ability to achieve its objectives and Kiromic's financing strategy and availability of funds. These forward-looking statements involve known and unknown risks, uncertainties and other factors that may cause actual results, levels of activity, performance, or achievements to be materially different from the information expressed or implied expressed or implied by these forward-looking statements. These risks and uncertainties include, but are not limited to, the risks and uncertainties discussed in our Annual Report on Form 10-K for the year ended December 31, 2022, and as detailed from time to time in our other SEC filings. You should not rely upon forward-looking statements as predictions of future events. Although we believe that the expectations reflected in the forward-looking statements are reasonable, we cannot guarantee that the future results, levels of activity, performance, or events and circumstances reflected in the forward-looking statements will be achieved or occur. Moreover, neither we nor any other person assumes responsibility for the accuracy and completeness of the forward-looking statements. Such forward-looking statements relate only to events as of the date of this press release. We undertake no obligation to update any forward-looking statements except to the extent required by law.

本新聞稿包含涉及重大風險和不確定性的前瞻性陳述。Kiromic根據美國《私人證券訴訟改革法》、經修訂的1934年《證券交易法》第21E條以及其他聯邦證券法的安全港條款做出此類前瞻性陳述。除歷史事實陳述以外的所有陳述均爲前瞻性陳述。在某些情況下,您可以通過諸如 “將”、“潛在”、“可能”、“可以”、“相信”、“打算”、“繼續”、“計劃”、“預期”、“預期”、“估計”、“可能” 等術語來識別前瞻性陳述,或者這些術語或其他類似術語的否定詞。這些前瞻性陳述包括但不限於以下方面的陳述:Kiromic實現其目標的能力、Kiromic的融資策略和資金可用性。這些前瞻性陳述涉及已知和未知的風險、不確定性和其他因素,這些因素可能導致實際結果、活動水平、業績或成就與這些前瞻性陳述所表達或暗示的信息存在重大差異。這些風險和不確定性包括但不限於我們在截至2022年12月31日止年度的10-K表年度報告中討論的風險和不確定性,以及我們在其他美國證券交易委員會文件中不時詳述的風險和不確定性。您不應依賴前瞻性陳述作爲對未來事件的預測。儘管我們認爲前瞻性陳述中反映的預期是合理的,但我們不能保證前瞻性陳述中反映的未來業績、活動水平、業績或事件和情況能夠實現或發生。此外,我們和任何其他人均不對前瞻性陳述的準確性和完整性承擔責任。此類前瞻性陳述僅與截至本新聞稿發佈之日的事件有關。除非法律要求,否則我們沒有義務更新任何前瞻性陳述。

Kiromic BioPharma
Linda Phelan Dyson, MPH
Global Head, Corporate Communications
ldyson@kiromic.com
281-468-7683

Kiromic BioPharm
Linda Phelan Dyson,MPH
企業傳播全球主管
ldyson@kiromic.com
281-468-7683

LHA Investor Relations
Tirth T. Patel
tpatel@lhai.com
212-201-6614

LHA 投資者關係
Tirth T. Patel
tpatel@lhai.com
212-201-6614

Beverly Hills Cancer Center
Sharon Neman
Chief Strategy Officer
SN@BHCancerCenter.com
310-432-8925

比佛利山莊癌症中心
莎朗·內曼
首席戰略官
SN@BHCancerCenter.com
310-432-8925

Source: Kiromic BioPharma, Inc.

來源:Kiromic BioPharma, Inc.

譯文內容由第三人軟體翻譯。


以上內容僅用作資訊或教育之目的,不構成與富途相關的任何投資建議。富途竭力但無法保證上述全部內容的真實性、準確性和原創性。
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