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CAMP4 to Participate in the Piper Sandler 36th Annual Healthcare Conference

CAMP4 to Participate in the Piper Sandler 36th Annual Healthcare Conference

CAMP4將參加派傑投資第36屆年度醫療保健大會
GlobeNewswire ·  2024/12/02 21:00

CAMBRIDGE, Mass., Dec. 02, 2024 (GLOBE NEWSWIRE) -- CAMP4 Therapeutics Corporation ("CAMP4") (Nasdaq: CAMP), a clinical-stage biotechnology company developing a pipeline of regRNA-targeting therapeutics designed to upregulate gene expression with the goal of restoring healthy protein levels across a range of genetic diseases, today announced that management will present and be available for one-on-one meetings at the Piper Sandler 36th Annual Healthcare Conference to be held at the Lotte New York Palace Hotel in New York City December 3rd – 5th, 2024.

馬薩諸塞州劍橋,2024年12月02日(環球新聞社) - CAMP4 Therapeutics Corporation(「CAMP4」)(納斯達克:CAMP),一家臨床階段的生物技術公司,正在開發一系列旨在通過調節反式轉錄核糖核酸(regRNA)靶點的治療藥物,以提高基因表達水平,旨在恢復各種遺傳疾病中健康蛋白水平的治療藥物管線,今天宣佈管理團隊將在2024年12月3日至5日於紐約市洛特紐約皇宮酒店舉行的派傑投資第36屆全球醫療保健大會上舉行演示並提供一對一會議。

Piper Sandler 36th Annual Healthcare Conference
Presentations Date: December 5, 2024
Time: 1:00-1:25 PM ET
Webcast Link: Click Here
派傑投資第36屆醫療保健年會
演示日期: 2024年12月5日
時間: 美東時間下午1:00-1:25
網絡直播鏈接: 點擊這裏

A live webcast of the presentation will be available via the Events section of the Company's investor relations website at

公司投資者關係網站的活動部分將提供本次演示的現場網絡廣播

To request a meeting or for more details about the conference, please reach out to your institutional contact or email.

想要預約會議或了解更多關於會議的詳情,請聯繫您的機構聯繫人或發送電子郵件。

About CAMP4 Therapeutics

關於 CAMP4 Therapeutics

CAMP4 is developing disease-modifying treatments for a broad range of genetic diseases where amplifying healthy protein may offer therapeutic benefits. Our approach amplifies mRNA by harnessing a fundamental mechanism of how genes are controlled. To amplify mRNA, our therapeutic ASO drug candidates target regRNAs, which act locally on transcription factors and are the master regulators of gene expression. CAMP4's proprietary RAP Platform enables the mapping of regRNAs and generation of therapeutic candidates designed to target the regRNAs associated with genes underlying haploinsufficient and recessive partial loss-of-function disorders, of which there are more than 1,200, in which a modest increase in protein expression may have the potential to be clinically meaningful. Learn more about us at and follow us on LinkedIn and X.

CAMP4 正在爲一系列遺傳疾病開發可改變疾病進程的治療方法,其中增加健康蛋白質可能會帶來治療益處。我們的方法通過利用基因受控的基本機制來增加 mRNA。爲了增加 mRNA,我們的治療 ASO 藥物候選品針對 regRNAs,這些 regRNAs 在轉錄因子上起作用,並且是基因表達的主要調節器。CAMP4 的專有 RAP 平台使得能夠對 regRNAs 進行映射,生成旨在靶向與單倍畸形和隱性部分功能喪失疾病相關基因的 regRNAs 的治療候選藥物,這類疾病超過 1,200 種,在其中增加蛋白質表達可能對臨床有意義。了解更多關於我們的信息並關注我們。 LinkedInX.

Forward-Looking Statements

前瞻性聲明

This press release contains forward-looking statements which involve risks, uncertainties and contingencies, many of which are beyond the control of the Company, which may cause actual results, performance, or achievements to differ materially from anticipated results, performance, or achievements. All statements other than statements of historical facts contained in this press release are forward-looking statements. In some cases, you can identify forward-looking statements by terms such as "may," "will," "should," "expect," "plan," "anticipate," "could," "intend," "target," "project," "contemplate," "believe," "estimate," "predict," "potential" or "continue" or the negative of these terms or other similar expressions, although not all forward-looking statements contain these words. Forward-looking statements include, but are not limited to, statements concerning CAMP4's plans, objectives, expectations and intentions; the timing and results of ongoing and future clinical trials, including expectations on the timing of reporting SAD and MAD data from and seeking regulatory approval for the CMP-CPS-001 trial; its growth strategy; and cash balance guidance. The forward-looking statements in this press release speak only as of the date of this press release and are subject to a number of known and unknown risks, uncertainties and assumptions that could cause the Company's actual results to differ materially from those anticipated in the forward-looking statements, including, but not limited to: the Company's limited operating history, incurrence of substantial losses since the Company's inception and anticipation of incurring substantial and increasing losses for the foreseeable future; the Company's need for substantial additional financing to achieve the Company's goals; the uncertainty of clinical development, which is lengthy and expensive, and characterized by uncertain outcomes, and risks related to additional costs or delays in completing, or failing to complete, the development and commercialization of the Company's current product candidates or any future product candidates; delays or difficulties in the enrollment and dosing of patients in clinical trials; the impact of any significant adverse events or undesirable side effects caused by the Company's product candidates; potential competition, including from large and specialty pharmaceutical and biotechnology companies; the Company's ability to realize the benefits of the Company's current or future collaborations or licensing arrangements and ability to successfully consummate future partnerships; the Company's ability to obtain regulatory approval to commercialize any product candidate in the United States or any other jurisdiction, and the risk that any such approval may be for a more narrow indication than the Company seeks; the Company's dependence on the services of the Company's senior management and other clinical and scientific personnel, and the Company's ability to retain these individuals or recruit additional management or clinical and scientific personnel; the Company's ability to grow the Company's organization, and manage the Company's growth and expansion of the Company's operations; risks related to the manufacturing of the Company's product candidates, which is complex, and the risk that the Company's third-party manufacturers may encounter difficulties in production; the Company's ability to obtain and maintain sufficient intellectual property protection for the Company's product candidates or any future product candidates the Company may develop; the Company's reliance on third parties to conduct the Company's preclinical studies and clinical trials; the Company's compliance with the Company's obligations under the licenses granted to the Company by others, for the rights to develop and commercialize the Company's product candidates; risks related to the operations of the Company's suppliers; and other risks and uncertainties described in the section "Risk Factors" in the Company's Quarterly Report on Form 10-Q for the quarter ended September 30, 2024, as well as other information we file with the Securities and Exchange Commission. The forward-looking statements in this press release are inherently uncertain and are not guarantees of future events. Because forward-looking statements are inherently subject to risks and uncertainties, some of which cannot be predicted or quantified and some of which are beyond the Company's control, you should not unduly rely on these forward-looking statements. The events and circumstances reflected in the forward-looking statements may not be achieved or occur and actual future results, levels of activity, performance and events and circumstances could differ materially from those projected in the forward-looking statements. Moreover, the Company operates in an evolving environment. New risks and uncertainties may emerge from time to time, and management cannot predict all risks and uncertainties. Investors, potential investors, and others should give careful consideration to these risks and uncertainties. Except as required by applicable law, the Company does not undertake to publicly update or revise any forward-looking statements contained herein, whether as a result of any new information, future events, changed circumstances or otherwise.

本新聞發佈包含涉及風險、不確定性和情況的前瞻性聲明,其中許多超出了公司的控制範圍,可能導致實際結果、績效或成就與預期的結果、績效或成就有實質不同。本新聞發佈中除歷史事實聲明外的所有陳述均爲前瞻性陳述。在某些情況下,您可以通過"可能"、"將會"、"應該"、"預期"、"計劃"、"預測"、"可能"、"打算"、"目標"、"項目"、"考慮"、"相信"、"估計"、"預測"、"潛在"或"繼續"等詞語來識別前瞻性陳述,儘管並非所有前瞻性陳述均包含這些詞語。前瞻性陳述包括但不限於關於CAMP4的計劃、目標、期望和意圖的聲明;正在進行中和未來臨床試驗的時間和結果,包括對從CMP-CPS-001試驗報告SAD和MAD數據以及尋求監管部門批准的時間的期望;其增長策略;和現金餘額指引。本新聞發佈中的前瞻性陳述僅適用於本新聞發佈的發佈日期,並受到一系列已知和未知風險、不確定因素和假設的影響,這可能導致公司的實際結果與前瞻性陳述中預期的結果有實質不同,包括但不限於:公司有限的營運歷史,自成立以來的巨額虧損以及預計在可預見的未來產生大量和增加虧損;公司需要大量額外融資以實現公司的目標;臨床開發的不確定性,這是漫長且昂貴的,並具有結果不確定性的特徵,包括完成或未完成開發和商業化公司當前產品候選藥物或任何未來產品候選藥物的附加成本或延遲的風險;在臨床試驗中招募和投藥患者的延遲或困難;由公司產品候選藥物引起的任何重大不良事件或不良副作用的影響;潛在的競爭,包括來自大型和專業製藥和生物技術公司的競爭;公司實現當前或未來合作伙伴關係或許可安排的好處併成功完成未來夥伴關係的能力;公司獲得監管批准,在美國或任何其他司法管轄區商業化任何產品候選藥物的能力,以及任何此類批准可能爲公司尋求的適應症更狹窄的風險;公司依賴公司高級管理層和其他臨床和科學人員的服務,以及公司留住這些人員或招募更多管理或臨床和科學人員的能力;公司發展公司的組織能力,以及管理公司的增長和公司運營拓展的風險;與公司產品候選藥物的製造有關的風險,這是複雜的,公司的第三方製造商可能會在生產中遇到困難;公司爲公司的產品候選藥物或公司將開發的任何未來產品候選藥物獲得並保持足夠的知識產權保護的能力;公司依賴第三方進行公司的臨床前和臨床試驗;公司遵守公司根據他人授予公司的許可在這些許可中公司開發和商業化公司的產品候選藥物的權利的義務;與公司供應商的運作有關的風險;以及公司在"風險因素"一節中描述的其他風險和不確定因素,這些風險和不確定因素在公司2024年9月30日結束的第10-Q表格季度報告和我們向美國證券交易委員會提交的其他信息中都有描述。本新聞發佈中的前瞻性陳述固有地不確定,並不是對未來事件的擔保。由於前瞻性陳述固有地受到風險和不確定性的影響,其中一些無法預測或量化,有些超出公司的控制,因此您不應過度依賴這些前瞻性陳述。前瞻性陳述所反映的事件和情況可能無法實現或發生,實際未來結果、活動水平、績效以及事件和情況可能會與前瞻性陳述中所預測的有實質不同。此外,公司運營在一個不斷髮展的環境中。新的風險和不確定性可能隨時出現,管理層無法預測所有風險和不確定因素。投資者、潛在投資者和其他人士應謹慎考慮這些風險和不確定因素。除非適用法律要求,公司不承諾公開更新或修訂本文中包含的任何前瞻性陳述,無論是否基於任何新信息、未來事件、變化的情況或其他原因。

Contacts

聯繫方式

Investor Relations:
Sandya von der Weid
LifeSci Advisors
svonderweid@lifesciadvisors.com

投資者關係:
Sandya von der Weid
LifeSci顧問
svonderweid@lifesciadvisors.com

Media:
Jason Braco, Ph.D.
LifeSci Communications
jbraco@lifescicomms.com

媒體:
Jason Braco, Ph.D.
通信-半導體
jbraco@lifescicomms.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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