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Jasper Therapeutics Announces First Patient Dosed in Phase 1b/2a SPOTLIGHT Clinical Study of Briquilimab in Chronic Inducible Urticaria

Jasper Therapeutics Announces First Patient Dosed in Phase 1b/2a SPOTLIGHT Clinical Study of Briquilimab in Chronic Inducible Urticaria

Jasper Therapeutics宣佈在治療慢性誘發性蕁麻疹的1b/2a期臨床研究中爲首位患者服用劑量
Jasper Therapeutics ·  03/19 12:00

REDWOOD CITY, Calif., March 19, 2024 (GLOBE NEWSWIRE) -- Jasper Therapeutics, Inc. (Nasdaq: JSPR) (Jasper), a biotechnology company focused on development of briquilimab, a novel antibody therapy targeting c-Kit (CD117) in mast cell driven diseases such as chronic spontaneous urticaria (CSU) and chronic inducible urticaria (CIndU), today announced that the first patient has been dosed in Jasper's Phase 1b/2a (SPOTLIGHT) clinical study of subcutaneous briquilimab for the treatment of CIndU. The SPOTLIGHT study is evaluating a single administration, at two different dose levels, of subcutaneous briquilimab in adult patients with cold urticaria (ColdU) or symptomatic dermographism (SD).

加利福尼亞州雷德伍德城,2024年3月19日(GLOBE NEWSWIRE)——專注於開發briquilimab的生物技術公司Jasper Therapeutics, Inc.(納斯達克股票代碼:Jsper)(Jasper)今天宣佈,這是一種針對慢性自發性蕁麻疹(CSU)和慢性誘發性蕁麻疹(CindU)等肥大細胞驅動疾病的C-kit(CD117)的新型抗體療法在賈斯珀的皮下布里曲利單抗治療CindU的1b/2a期(SPOTLIGHT)臨床研究中,第一位患者已經服用了劑量。SPOTLIGHT研究正在評估在感冒性蕁麻疹(ColDU)或有症狀的皮膚造影術(SD)的成年患者中,在兩種不同的劑量水平下單次使用briquilimab。

"We are excited to announce dosing of the first patient in the SPOTLIGHT study in patients with CIndU, our second clinical program evaluating briquilimab in a mast cell-mediated disease," said Edwin Tucker, Chief Medical Officer of Jasper. "As with our BEACON study in CSU, we expect the SPOTLIGHT study to establish proof of concept for the depletion of mast cells by briquilimab in CIndU and help us to determine doses and dosing regimens for future registrational studies. We plan to provide enrollment updates as we progress through the study and anticipate reporting preliminary data in the second half of 2024."

賈斯珀首席醫學官埃德溫·塔克說:“我們很高興地宣佈,SPOTLIGHT研究中的第一位患者在CindU患者中給藥,這是我們第二個評估briquilimab治療肥大細胞介導疾病的臨床項目。”“與我們在科羅拉多州立大學的BEACON研究一樣,我們預計SPOTLIGHT研究將爲briquilimab在CindU中消耗肥大細胞提供概念驗證,並幫助我們爲未來的註冊研究確定劑量和給藥方案。隨着研究的進展,我們計劃提供最新入學情況,並預計將在2024年下半年報告初步數據。”

The SPOTLIGHT study is expected to enroll approximately 15 patients across 2 dose cohorts. The primary endpoints are safety and tolerability of briquilimab with secondary endpoints focused on efficacy measures and pharmacokinetics. The study is being conducted at four sites in the EU. Jasper anticipates reporting preliminary data from the SPOTLIGHT study in the second half of 2024.

SPOTLIGHT研究預計將在2個劑量隊列中招收約15名患者。主要終點是briquilimab的安全性和耐受性,次要終點側重於療效指標和藥代動力學。該研究正在歐盟的四個地點進行。賈斯珀預計將在2024年下半年報告SPOTLIGHT研究的初步數據。

"c-Kit inhibitors are a promising class of monoclonal therapeutics with demonstrated efficacy in mast cell driven diseases," said Marcus Maurer, M.D., Professor of Dermatology and Allergy at Charité – Universitätsmedizin in Berlin. "As a potent and differentiated c-Kit inhibitor, I believe briquilimab has the potential to serve as an important treatment option for patients suffering from CIndU, and I look forward to enrolling patients into the SPOTLIGHT study and additionally into the BEACON study for CSU."

柏林查裏特大學皮膚病學和過敏學教授馬庫斯·毛雷爾醫學博士說:“C-kit抑制劑是一類前景看好的單克隆療法,在肥大細胞驅動的疾病中已顯示出療效。”“作爲一種有效的差異化C-kit抑制劑,我相信briquilimab有可能成爲CindU患者的重要治療選擇,我期待着讓患者參與SPOTLIGHT研究以及科羅拉多州立大學的BEACON研究。”

About Briquilimab

關於 briquilimab

Briquilimab (formerly JSP191) is a targeted aglycosylated monoclonal antibody that blocks stem cell factor from binding to the cell-surface receptor c-Kit, also known as CD117, thereby inhibiting signaling through the receptor. This inhibition disrupts the critical survival signal, leading to the depletion of the mast cells via apoptosis which removes the underlying source of the inflammatory response in mast cell driven diseases such as chronic urticaria. Jasper is currently conducting clinical studies of briquilimab as a treatment in patients with CSU or with CIndU. Briquilimab is also currently in clinical studies as a treatment for patients with LR-MDS and as a conditioning agent for cell therapies for rare diseases. To date, briquilimab has a demonstrated efficacy and safety profile in more than 145 dosed participants and healthy volunteers, with clinical outcomes as a conditioning agent in severe combined immunodeficiency (SCID), AML, MDS, FA, and sickle cell disease (SCD).

Briquilimab(前身爲 JSP191)是一種靶向的糖基化單克隆抗體,可阻止幹細胞因子與細胞表面受體 C-kit(也稱爲 CD117)結合,從而抑制通過受體的信號傳導。這種抑制會干擾關鍵的存活信號,通過細胞凋亡導致肥大細胞消耗,從而消除肥大細胞驅動的疾病(例如慢性蕁麻疹)炎症反應的潛在來源。賈斯珀目前正在對briquilimab作爲科羅拉多州立大學或CinDU患者的治療藥物進行臨床研究。Briquilimab目前也在臨床研究中,它既是LR-MDS患者的治療方法,也是罕見疾病細胞療法的調理劑。迄今爲止,briquilimab在超過145名給藥參與者和健康志願者中具有顯著的療效和安全性,作爲重度聯合免疫缺陷(SCID)、急性髓細胞白血病、MDS、FA和鐮狀細胞病(SCD)的調理劑具有臨床療效。

About Jasper

關於賈斯珀

Jasper is a clinical-stage biotechnology company developing briquilimab, a monoclonal antibody targeting c-Kit (CD117) as a therapeutic for chronic mast and stem cell diseases such as chronic urticaria and lower to intermediate risk MDS and as a conditioning agent for stem cell transplants for rare diseases such as SCD, FA and SCID. To date, briquilimab has a demonstrated efficacy and safety profile in more than 145 dosed participants and healthy volunteers, with clinical outcomes as a conditioning agent in SCID, AML, MDS, FA, and SCD. For more information, please visit us at www.jaspertherapeutics.com.

Jasper是一家處於臨床階段的生物技術公司,正在開發briquilimab,這是一種靶向 c-kit (CD117) 的單克隆抗體,用於治療慢性蕁麻疹和低至中等風險 MDS 等慢性肥大和幹細胞疾病,並作爲 SCD、FA 和 SCID 等罕見疾病幹細胞移植的調節劑。迄今爲止,briquilimab在超過145名給藥參與者和健康志願者中已得到證實的療效和安全性,作爲SCID、AML、MDS、FA和SCD的調理劑,其臨床結果爲調理劑。欲了解更多信息,請訪問我們的網站 www.jaspertherapeut

Forward-Looking Statements

前瞻性陳述

Certain statements included in this press release that are not historical facts are forward-looking statements for purposes of the safe harbor provisions under the United States Private Securities Litigation Reform Act of 1995. Forward-looking statements are sometimes accompanied by words such as "believe," "may," "will," "estimate," "continue," "anticipate," "intend," "expect," "should," "would," "plan," "predict," "potential," "seem," "seek," "future," "outlook" and similar expressions that predict or indicate future events or trends or that are not statements of historical matters. These forward-looking statements include, but are not limited to, statements regarding briquilimab's potential, including with respect to its potential in mast cell driven diseases such as CSU and CIndU and its potential to serve as an important treatment option for patients suffering from CIndU; Jasper's expectations regarding its Phase 1b/2a SPOTLIGHT study of subcutaneous briquilimab in CIndU, including the expected enrollment, cohorts and site locations, the expected timing for reporting preliminary data, the expectation that the SPOTLIGHT or BEACON studies will establish proof of concept or help Jasper determine doses and dosing regimens for future registrational studies; and Jasper's expectations regarding its BEACON study in CSU, including the expectation that Jasper will enroll additional patients in the BEACON study for CSU. These statements are based on various assumptions, whether or not identified in this press release, and on the current expectations of Jasper and are not predictions of actual performance. These forward-looking statements are provided for illustrative purposes only and are not intended to serve as, and must not be relied on by an investor as, a guarantee, an assurance, a prediction or a definitive statement of fact or probability. Many actual events and circumstances are beyond the control of Jasper. These forward-looking statements are subject to a number of risks and uncertainties, including general economic, political and business conditions; the risk that the potential product candidates that Jasper develops may not progress through clinical development or receive required regulatory approvals within expected timelines or at all; the risk that clinical trials may not confirm any safety, potency or other product characteristics described or assumed in this press release; the risk that Jasper will be unable to successfully market or gain market acceptance of its product candidates; the risk that prior study results may not be replicated; the risk that Jasper's product candidates may not be beneficial to patients or successfully commercialized; patients' willingness to try new therapies and the willingness of physicians to prescribe these therapies; the effects of competition on Jasper's business; the risk that third parties on which Jasper depends for laboratory, clinical development, manufacturing and other critical services will fail to perform satisfactorily; the risk that Jasper's business, operations, clinical development plans and timelines, and supply chain could be adversely affected by the effects of health epidemics; the risk that Jasper will be unable to obtain and maintain sufficient intellectual property protection for its investigational products or will infringe the intellectual property protection of others; and other risks and uncertainties indicated from time to time in Jasper's filings with the SEC, including its Annual Report on Form 10-K for the year ended December 31, 2023 and subsequent Quarterly Reports on Form 10-Q. If any of these risks materialize or Jasper's assumptions prove incorrect, actual results could differ materially from the results implied by these forward-looking statements. While Jasper may elect to update these forward-looking statements at some point in the future, Jasper specifically disclaims any obligation to do so. These forward-looking statements should not be relied upon as representing Jasper's assessments of any date subsequent to the date of this press release. Accordingly, undue reliance should not be placed upon the forward-looking statements.

就1995年《美國私人證券訴訟改革法》的安全港條款而言,本新聞稿中包含的某些非歷史事實的陳述是前瞻性陳述。前瞻性陳述有時伴隨着諸如 “相信”、“可能”、“將”、“估計”、“繼續”、“預測”、“打算”、“預期”、“應該”、“將”、“計劃”、“潛在”、“看來”、“尋找”、“未來”、“展望” 等詞語以及預測或表明未來事件或趨勢或不是歷史問題陳述的類似表達。這些前瞻性陳述包括但不限於有關briquilimab潛力的陳述,包括其在科羅拉多州立大學和CindU等肥大細胞驅動疾病中的潛力及其作爲CindU患者重要治療選擇的潛力;賈斯珀對CindU皮下briquilimab的1b/2a期SPOTLIGHT研究,包括預期入組、隊列和研究地點的預期,報告初步數據的預期時間,SPOTLIGHT或BEACON研究的期望將建立概念驗證或幫助賈斯珀確定未來註冊研究的劑量和給藥方案;以及賈斯珀對科羅拉多州立大學BEACON研究的期望,包括預計賈斯珀將在科羅拉多州立大學的BEACON研究中招收更多患者。這些陳述基於各種假設,無論是否在本新聞稿中提出,也基於賈斯珀當前的預期,不是對實際業績的預測。這些前瞻性陳述僅用於說明目的,無意用作擔保、保證、預測或明確的事實或概率陳述,投資者也不得依賴這些陳述作爲擔保、保證、預測或明確的事實或概率陳述。許多實際事件和情況都超出了賈斯珀的控制範圍。這些前瞻性陳述受許多風險和不確定性的影響,包括總體經濟、政治和商業狀況;賈斯珀開發的潛在候選產品可能無法在預期的時間表內或根本無法通過臨床開發取得進展或獲得所需的監管部門批准的風險;臨床試驗可能無法證實本新聞稿中描述或假設的任何安全性、效力或其他產品特徵的風險;賈斯珀無法成功上市或獲得市場認可的風險其候選產品;先前研究結果無法複製的風險;賈斯珀的候選產品可能無法使患者受益或無法成功商業化的風險;患者嘗試新療法的意願和醫生開這些療法的意願;競爭對賈斯珀業務的影響;賈斯珀賴以提供實驗室、臨床開發、製造和其他關鍵服務的第三方無法令人滿意地表現的風險;賈斯珀的風險 Per 的業務、運營、臨床發展計劃和時間表以及供應鏈可能會受到以下因素的不利影響:健康流行病的影響;賈斯珀無法爲其研究產品獲得和維持足夠的知識產權保護或侵犯他人知識產權保護的風險;以及賈斯珀向美國證券交易委員會提交的文件中不時指出的其他風險和不確定性,包括其截至2023年12月31日止年度的10-K表年度報告和隨後的表格季度報告 10-Q。如果其中任何風險得以實現或賈斯珀的假設被證明不正確,則實際結果可能與這些前瞻性陳述所暗示的結果存在重大差異。儘管賈斯珀可能會選擇在未來的某個時候更新這些前瞻性陳述,但賈斯珀明確表示不承擔任何更新這些前瞻性陳述的義務。不應將這些前瞻性陳述視爲賈斯珀對本新聞稿發佈之日後任何日期的評估。因此,不應過分依賴前瞻性陳述。

Contacts:

聯繫人:

Joyce Allaire (investors)
LifeSci Advisors
617-435-6602
jallaire@lifesciadvisors.com

喬伊斯·阿萊爾(投資者)
生命科學顧問
617-435-6602
jallaire@lifesciadvisors.com

Alex Gray (investors)
Jasper Therapeutics
650-549-1454
agray@jaspertherapeutics.com

亞歷克斯·格雷(投資者)
賈斯珀療法
650-549-1454
agray@jaspertherapeutics.com

Lauren Walker (media)
Real Chemistry
646-564-2156
lbarbiero@realchemistry.com

勞倫·沃克(媒體)
真正的化學
646-564-2156
lbarbiero@realchemistry.com

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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