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NKGen Biotech Announces FDA Clearance Of IND Application For SNK01 NK Cell Therapy in Parkinson's Disease

NKGen Biotech Announces FDA Clearance Of IND Application For SNK01 NK Cell Therapy in Parkinson's Disease

NKGen Biotech宣布美国食品药品管理局批准帕金森氏病的 SNK01 NK 细胞疗法的临床申请
Benzinga ·  04/29 08:08

NKGen advances its neurodegenerative disease program with FDA IND clearance for its Phase 1/2a SNK01 Clinical Trial in patients with Parkinson's disease.

NKGen推进其神经退行性疾病项目,美国食品药品管理局批准了其针对帕金森氏病患者的1/2a期 SNK01 临床试验。

The Company expects to initiate a Phase 1 clinical trial in PD in 2H 2024.

该公司预计将在2024年下半年启动PD的1期临床试验。

SANTA ANA, Calif., April 29, 2024 (GLOBE NEWSWIRE) -- NKGen Biotech, Inc. (NASDAQ:NKGN) ("NKGen" or the "Company"), a clinical-stage biotechnology company focused on the development and commercialization of innovative autologous, allogeneic and CAR-NK natural killer ("NK") cell therapeutics, today announced that the U.S. Food and Drug Administration ("FDA") has cleared the Company's Investigational New Drug ("IND") application for SNK01 NK cell therapy for the treatment of Parkinson's disease ("PD"). SNK01 is an autologous, nongenetically modified NK cell product that has enhanced cytotoxicity and activating receptor expression, potentially addressing a novel approach to tackling Parkinson's disease.

加利福尼亚州圣安娜,2024年4月29日(GLOBE NEWSWIRE)——专注于创新自体、异基因和CAR-NK自然杀手(“NK”)细胞疗法开发和商业化的临床阶段生物技术公司 NKGen Biotech, Inc.(纳斯达克股票代码:NKGN)(“NKGen” 或 “公司”)今天宣布,美国食品药品监督管理局(“FDA”)已批准该公司用于治疗帕金森氏病(“PD”)的 SNK01 NK细胞疗法的研究性新药(“IND”)申请。SNK01 是一种自体、非基因改造的 NK 细胞产物,具有增强细胞毒性并激活受体表达,有可能解决一种治疗帕金森氏病的新方法。

The FDA IND clearance enables NKGen to initiate a Phase 1/2a clinical trial evaluating the safety, tolerability, and exploratory efficacy of SNK01 in patients with PD. The trial is designed to enroll up to 30 patients (20 receiving SNK01 and 10 receiving placebo). NKGen expects to begin the trial, with the first patient dosed, in the second half of 2024.

美国食品药品管理局的IND批准使NKGen能够启动一项1/2a期临床试验,评估 SNK01 对PD患者的安全性、耐受性和探索性疗效。该试验旨在招收多达 30 名患者(20 名接受 SNK01,10 名接受安慰剂)。NKGen预计将在2024年下半年开始试验,为第一位患者服药。

"The IND clearance marks a significant milestone as we advance our pipeline of NK cell therapy in neurodegenerative diseases," said Paul Y. Song, MD, Chairman and Chief Executive Officer of NKGen. "This is our second IND approval for SNK01 within the past several months and underscores our focused dedication towards developing safe and effective treatments that target both protein deposition and neuroinflammation for patients with neurodegenerative diseases such as Alzheimer's and Parkinson's. We are excited to start our first clinical trial in PD as there currently is a high unmet medical need in this indication."

NKGen董事长兼首席执行官Paul Y. Song医学博士表示:“在我们推进神经退行性疾病NK细胞疗法产品线的过程中,IND的批准标志着一个重要的里程碑。”“这是我们在过去几个月内第二次获得 SNK01 的IND批准,这凸显了我们致力于为阿尔茨海默氏症和帕金森氏症等神经退行性疾病患者开发针对蛋白质沉积和神经炎症的安全有效的治疗方法。我们很高兴在PD开始我们的第一项临床试验,因为目前该适应症有大量未得到满足的医疗需求。”

Dr. Song further commented, "Given the encouraging outcomes regarding the reduction in neuroinflammation observed in our Phase 1 Alzheimer's trials, we are optimistic about the potential benefits that may emerge in our Parkinson's trial. Although these two neurodegenerative diseases differ, both share a neuroinflammatory component, which has led to our hypothesis that SNK01 may be beneficial in both indications. While directly inhibiting neuroinflammation, whether as an independent approach or in conjunction with other interventions, may not address the etiology, it can potentially decrease the production of factors that contribute to neurotoxicity, thereby hopefully leading to clinical improvements."

宋博士进一步评论说:“鉴于我们在1期阿尔茨海默氏症试验中观察到的减少神经炎症的令人鼓舞的结果,我们对帕金森氏症试验可能产生的潜在益处持乐观态度。尽管这两种神经退行性疾病不同,但它们都具有神经炎性成分,这使我们假设 SNK01 可能对两种适应症都有益。尽管直接抑制神经炎症,无论是作为独立方法还是与其他干预措施结合使用,都可能无法解决病因,但它有可能减少导致神经毒性的因子的产生,从而有望带来临床改善。”

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