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Jasper Therapeutics Presents Data From Preclinical Briquilimab Study at the 2024 EHA Hybrid Congress

Jasper Therapeutics Presents Data From Preclinical Briquilimab Study at the 2024 EHA Hybrid Congress

Jasper Therapeutics在2024年EHA混合大會上展示了Briquilimab的臨床前研究數據
Jasper Therapeutics ·  06/14 12:00

REDWOOD CITY, Calif., June 14, 2024 (GLOBE NEWSWIRE) -- Jasper Therapeutics, Inc. (Nasdaq: JSPR) (Jasper), a clinical stage biotechnology company focused on development of briquilimab, a novel antibody therapy targeting c-Kit (CD117) to address mast cell driven diseases such as chronic spontaneous urticaria (CSU), chronic inducible urticaria (CIndU) and asthma, today is presenting preclinical data demonstrating the effect of briquilimab on hematopoietic stem cells (HSCs) at the European Hematology Association (EHA) Hybrid Congress, being held June 13 – 16, 2024 in Madrid, Spain.

加利福尼亞州紅木城,2024年6月14日,全球新聞社——Jasper Therapeutics,Inc.(納斯達克股票代碼:JSPR)(簡稱Jasper)——一家專注於生物技術,臨床階段的生物技術公司,致力於開發靶向c-Kit(CD117)的新型抗體治療藥物briquilimab來治療由肥大細胞驅動的疾病,如慢性自發性蕁麻疹(CSU)、慢性誘發性蕁麻疹(CIndU)和哮喘,今天在西班牙馬德里舉行的2024年歐洲血液學會(EHA)混合大會上,發佈了展示briquilimab對造血幹細胞(HSCs)作用的臨床前數據。

The study being presented evaluated the molecular basis of inhibition of the stem cell factor (SCF)/c-Kit signaling pathway via briquilimab and its functional impact on healthy human HSC survival, proliferation, and differentiation. Results from the study demonstrate that blocking of SCF/c-Kit signaling by briquilimab does not cause apoptosis of HSCs, and that HSCs cultured in the presence of briquilimab differentiate directly into CD34- cells with higher c-Kit expression and without increased CD38 expression.

該研究評估了通過briquilimab 抑制幹細胞因子(SCF)/ c-Kit信號通路的分子基礎及其對健康人HSC的存活、增殖和分化的功能影響。研究結果表明,briquilimab 對 SCF/c-Kit信號的阻斷並未導致HSC的凋亡,而在briquilimab存在下培養的HSCs則直接分化成CD34-細胞,並具有更高的c-Kit表達而沒有增加的CD38表達。

"We are pleased to present preclinical data demonstrating the effect of c-Kit inhibition on the HSC compartment," said Wendy Pang, M.D., Ph.D., Senior Vice President, Research and Translational Medicine of Jasper. "While blocking of SCF/c-Kit signaling by briquilimab does lead to mast cell apoptosis, it is important that it does not have a similar effect on healthy HSCs, and these data indicate that briquilimab instead skews them towards a distinct alternative HSC differentiation pathway. We believe the results of the study align with those observed to-date in clinical trials of anti-c-Kit agents and support the safety profile of briquilimab in mast cell diseases."

“我們很高興呈現臨床前數據,展示c-Kit抑制劑對HSC組成的影響,”Jasper的研究與轉化醫學高級副總裁鄧雯醫學博士表示。“雖然briquilimab抑制SCF/c-Kit信號通路可以導致肥大細胞凋亡,但它不會對健康HSCs產生類似的影響,這些數據表明briquilimab將其偏向於不同的HSC分化通路。我們認爲研究結果與迄今爲止抗c-Kit藥物的臨床試驗觀察結果相一致,並支持briquilimab在肥大細胞疾病的安全性資料”。

Details of the presentation are below:

演示的細節如下:

Title: Briquilimab Potently Inhibits SCF/c-Kit Signaling, Which Does Not Induce Healthy HSC Apoptosis, But Skews HSC Differentiation Potential
Abstract Number: P1391
Session Type: Poster Session
Session Title: Hematopoiesis, Stem Cells and Microenvironment
Location: Poster Area (Hall 7)
Date/Time: Friday, June 14, 2024; 6:00-7:00pm CEST

標題:Briquilimab Potently Inhibits SCF/c-Kit Signaling, Which Does Not Induce Healthy HSC Apoptosis, But Skews HSC Differentiation Potential
摘要編號:P1391
會議類型:海報展示會議
會議主題:造血、幹細胞和微環境
地點:海報區域(第7廳)
日期/時間:2024年6月14日(星期五);夏令時下午6:00-7:00

The presentation will be available on the EHA website as well as the events page on the Jasper Therapeutics IR website.

展示將在歐洲血液學會網站和Jasper Therapeutics IR網站上提供。公司的投資者關係網站的事件頁面在Jasper Therapeutics IR網站上。

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, and is planning to initiate a clinical study in patients with asthma. 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), acute myeloid leukemia (AML), myelodysplastic syndromes (MDS), Fanconi anemia (FA), and sickle cell disease (SCD).

Briquilimab(前稱JSP191)是一種目標化的非糖基化單克隆抗體,可阻止幹細胞因子與細胞表面受體c-Kit,即CD117的結合,從而抑制受體信號。這種抑制會破壞關鍵的生存信號,通過自噬促使肥大細胞減少,從而去除由肥大細胞驅動的炎症反應。Jasper目前正在進行briquilimab在患有CSU或CIndU患者中作爲治療藥物的臨床研究,並計劃開始一項在哮喘患者中的研究。Briquilimab目前也正在進行作爲治療LR-MDS的患者和作爲細胞療法稀有疾病的條件製劑的患者的臨床研究。迄今爲止,briquilimab在145名受試者和健康志願者中證明具有實際功效和安全性,並且在嚴重聯合免疫缺陷(SCID)、急性髓細胞白血病(AML)、骨髓增生異常綜合症(MDS)、Fanconi貧血(FA)和鐮狀細胞病(SCD)作爲條件製劑的臨床結果。

About Jasper

關於Jasper

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是一家臨床階段的生物技術公司,正在開發靶向c-Kit(CD117)的單克隆抗體briquilimab,作爲治療慢性肥大細胞和幹細胞疾病的治療藥物,例如慢性蕁麻疹和低到中風險的MDS,並作爲肥大細胞病、FA和SCID等罕見病Stem cells治療移植的製劑。到目前爲止,briquilimab已經在145名受試者和健康志願者中證明具有實際功效和安全性,並具有SCID、AML、MDS、FA和SCD的臨床結果。欲了解更多信息,請訪問我們的網站:www.jaspertherapeutics.com.

Forward-Looking Statements

前瞻性聲明

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, CIndU, and asthma, its ability to block SCF/c-Kit signaling and not cause apoptosis of HSCs, the potential for HSCs cultured in the presence of briquilimab to differentiate directly into CD34- cells with higher c-Kit expression and without increased CD38 expression, its ability to skew healthy HSCs towards a distinct alternative HSC differentiation pathway, and the safety profile of briquilimab in mast cell diseases. 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.

本新聞稿中包含的某些不是歷史事實的陳述,是針對1995年美國私人證券訴訟改革法安全港規定的前瞻性陳述。前瞻性陳述有時會伴隨着諸如“相信”、“可能”、“將”、“估計”、“繼續”、“預期”、“應該”、“願意”、“規劃”、“預測”、“潛在”、“看起來”、“尋找”、“未來”、“前景”等的詞語,預測或指示未來事件或趨勢,或者不是歷史事實陳述這些語言。這些前瞻性陳述包括但不限於有關briquilimab的潛力,包括其在肥大細胞驅動的疾病,如CSU、CIndU和哮喘中的潛力,其阻止SCF/c-Kit信號且不會引起HSCs凋亡的能力,存在briquilimab的情況下培養的HSCs分化成CD34-細胞並具有更高的c-Kit表達而沒有增加CD38表達的潛力,偏向於不同的HSC分化通路以維持健康的HSC的能力,以及在肥大細胞疾病中briquilimab的安全性資料。這些語句基於各種假設,無論此新聞稿中是否已確定,並且基於Jasper的當前預期,而不是實際表現的預測。這些前瞻性陳述僅供說明目的,不打算作爲投資者的保證、保證、預測或事實或概率的明確陳述。許多實際事件和情況都超出了Jasper的控制範圍。這些前瞻性陳述受到一系列風險和不確定性的影響,包括一般經濟、政治和商業條件; Jasper開發的潛在產品候選品可能不會按預期時間表或根本不會在臨床發展中進展或獲得所需的監管批准; 臨床試驗可能無法證實本新聞稿中所描述或假設的任何安全性、效力或其他產品特性; Jasper將無法成功市場或獲得其產品候選品的市場接受; 先前的研究結果可能無法複製; Jasper的產品候選品可能對患者沒有益處或沒有成功商業化; 患者願意嘗試新療法以及醫生開處方這些療法的意願; 競爭對Jasper的業務產生的影響; 依賴Jasper進行實驗室、臨床開發、製造和其他重要服務的第三方未能令人滿意地執行; 健康流行病的影響可能會影響Jasper的業務、運營、臨床開發計劃和時間表以及供應鏈; Jasper將無法爲其實驗室研究、臨床開發、製造和其他關鍵服務獲得充分的知識產權保護,或將侵犯他人的知識產權保護; 其他Jasper在SEC的提交文件中不時表明的風險和不確定性,包括其於2023年12月31日結束的年度報告正式入場申請書和其隨後的季度報告正式入場申請書。如果這些風險中的任何一項成爲現實,或Jasper的假設證明不正確,則與這些前瞻性陳述所暗示的結果可能有很大不同。雖然Jasper可能會在未來某個時間選擇更新這些前瞻性陳述,但Jasper明確聲明不承擔任何義務這樣做。這些前瞻性陳述不應被視爲Jasper對本新聞稿日期之後的任何日期的評估。因此,不應過分依賴這些前瞻性陳述。

Contacts:

聯繫人:

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

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

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

Alex Gray(投資人)
Jasper治療
650-549-1454
agray@jaspertherapeutics.com

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

Lauren Walker(媒體)
Real Chemistry
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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