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Kiromic BioPharma Announces Deltacel Phase 1 Clinical Trial Enters Patient Recruitment Phase at Beverly Hills Cancer Center

Kiromic BioPharma Announces Deltacel Phase 1 Clinical Trial Enters Patient Recruitment Phase at Beverly Hills Cancer Center

Kiromic BioPharma 宣佈 Deltacel 1 期臨床試驗在比佛利山莊癌症中心進入患者招募階段
Kiromic BioPharma ·  2023/11/09 13:00

Company is Activating Additional Clinical Trial Sites Across the U.S.

公司正在激活美國各地的更多臨床試驗基地

HOUSTON--(BUSINESS WIRE)--Nov. 9, 2023--

休斯頓--(美國商業資訊)--2023年11月9日--

Kiromic BioPharma, Inc. (OTC PINK: 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, announces the Deltacel Phase 1 Clinical Trial is now recruiting patients at the Beverly Hills Cancer Center (BHCC). The study will evaluate Deltacel (KB-GDT-01), Kiromic's allogeneic, off-the-shelf, Gamma Delta T-cell (GDT) therapy, in patients with metastatic non-small cell lung cancer (NSCLC).

Kiromic BioPharma, Inc.(OTC PINK:KRBP)(“KRBP” 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 Deltacel宣佈,用於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 1期臨床試驗目前正在比佛利山莊癌症中心(BHCC)招募患者。該研究將評估 Deltacel (KB-GDT-01),Kiromic的異基因、現成伽瑪三角洲T細胞(GDT)療法,適用於轉移性非小細胞肺癌(NSCLC)患者。

The Company continues to engage additional clinical trial sites across the U.S, and will provide updates as additional sites are activated, and as patient recruitment starts at those locations.

該公司將繼續在美國各地聘請更多臨床試驗場所,並將在其他地點啓動以及在這些地點開始招募患者時提供最新信息。

The Phase 1 trial, titled "Safety Study for a Gamma Delta T Cell Product Used With Low Dose Radiotherapy in Patients With Stage 4 Metastatic NSCLC" (ID# NCT06069570), expects to enroll up to 48 patients. In this open-label, two-part trial, patients with stage 4 NSCLC will receive two intravenous infusions of Deltacel along with four courses of low-dose, localized radiation, over a 10-day period. The primary objective of the study is to evaluate the safety of Deltacel in combination with low-dose radiation; the secondary outcome measures are objective response, progression-free survival, overall survival, time to progression, time to treatment response, and disease control rates.

這項 1 期試驗名爲 “用於低劑量放射治療的 Gamma Delta T 細胞產品對第 4 期轉移性 NSCLC 患者的安全性研究”(ID# NCT06069570),預計將招收多達48名患者。在這項由兩部分組成的開放標籤試驗中,4期非小細胞肺癌患者將在10天內接受兩次Deltacel靜脈輸液以及四個療程的低劑量局部放射治療。該研究的主要目的是評估Deltacel與低劑量輻射聯合使用的安全性;次要結果指標是客觀反應、無進展存活率、總體存活率、進展時間、治療反應時間和疾病控制率。

"We are delighted to announce the start of patient recruitment in our first clinical trial, and we look forward to working with BHCC and the other prestigious trial sites we will be activating across the U.S. Importantly, we are on target to dose our first patient, and we expect to have early tolerability and safety data from this patient available by the end of 2023," stated Pietro Bersani, Chief Executive Officer of Kiromic BioPharma. "We plan to assess preliminary efficacy by end of January 2024, and complete the dose-escalation portion of the study by the second half of 2024, at which point we expect to have sufficient evidence supporting the tolerability and the efficacy of Deltacel. These are crucial steps forward as we advance our goal to bring a transformative new treatment to patients with advanced NSCLC."

Kiromic BioPharma首席執行官彼得羅·貝爾薩尼表示:“我們很高興地宣佈我們的第一項臨床試驗開始招募患者,我們期待與BHCC以及我們將在美國各地啓動的其他著名試驗機構合作。重要的是,我們的目標是爲第一位患者提供劑量,我們預計將在2023年底之前獲得該患者的早期耐受性和安全性數據。”“我們計劃在2024年1月底之前評估初步療效,並在2024年下半年之前完成研究的劑量遞增部分,屆時我們預計將有足夠的證據支持Deltacel的耐受性和療效。在我們推進爲晚期非小細胞肺癌患者提供變革性新療法的目標的過程中,這些是向前邁出的關鍵一步。”

About Deltacel (KB-GDT-01)

關於 Deltacel (KB-GDT-01)

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 non–small cell lung cancer. An allogeneic product consisting of unmodified, donor-derived gamma delta T cells, Deltacel is Kiromic BioPharma's lead candidate in its 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)是一種在研的伽瑪三角洲T細胞(GDT)療法,目前正在進行Deltacel-01 1期試驗,用於治療非小細胞肺癌。Deltacel是一種由未經修飾的捐贈者衍生的伽瑪三角洲T細胞組成的異基因產品,是Kiromic BioPharma在其GDT平台上的主要候選藥物。Deltacel旨在利用GDT細胞的天然效力來靶向實體癌,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%。來自兩項臨床前研究的數據表明,當Deltacel與低劑量輻射結合使用時,它具有良好的安全性和有效性。

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 state-of-the-art cancer treatment modalities all under one roof, but also leading clinical trials and research for cancer that are offered at very few centers in the world, attracting patients globally and saving lives. By providing access to groundbreaking clinical trials, the Beverly Hills Cancer Center offers patients the opportunity to participate in the most advanced cancer treatments in development in the world. Beverly Hills Cancer Center is comprised 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. For more information, visit: www.bhcancercenter.com.

作爲一傢俬人、學術和社區癌症中心,比佛利山癌症中心不僅在一個屋檐下提供最先進的癌症治療方式,而且還領先的癌症臨床試驗和研究,這些試驗和研究在世界上很少有中心提供,吸引了全球患者並挽救了生命。通過提供開創性的臨床試驗,比佛利山莊癌症中心爲患者提供了參與世界上最先進的癌症治療方法的機會。比佛利山癌症中心由國際認可的多學科醫療團隊組成,該團隊由腫瘤內科醫生、放射腫瘤學家、放射科醫生、血液學家和內科醫生組成,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。欲了解更多信息,請訪問: www.bhcancercenter.co

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目標識別相結合的地方,它可以顯著縮短開發活藥所需的年限和數億美元。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

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》的安全港條款、經修訂的1934年《證券交易法》第21E條以及其他聯邦證券法作出此類前瞻性陳述。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,你可以用諸如 “將”、“潛在”、“可能”、“可以”、“相信”、“打算”、“繼續”、“計劃”、“預期”、“預期”、“預期”、“估計”、“可能” 或這些術語或其他類似術語的負面詞彙來識別前瞻性陳述。這些前瞻性陳述包括但不限於有關以下方面的陳述:Kiromic實現目標的能力以及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業績、活動水平、業績或成就與這些前瞻性陳述所表達或暗示的明示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,以及我們在美國證券交易委員會的其他文件中不時詳細介紹的風險和不確定性。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

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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