BioCardia Announces Positive Consultation With Japan PMDA on CardiAMP Cell Therapy for Ischemic Heart Failure
BioCardia Announces Positive Consultation With Japan PMDA on CardiAMP Cell Therapy for Ischemic Heart Failure
Next PMDA Consultation after Review of CardiAMP HF Trial Data
下一次PMDA諮詢將在CardiAMP心衰試驗數據審查後進行
SUNNYVALE, Calif., Dec. 04, 2024 (GLOBE NEWSWIRE) -- BioCardia, Inc. [Nasdaq: BCDA], a global leader in cellular and cell-derived therapeutics for the treatment of cardiovascular and pulmonary diseases, announced today the successful completion of a consultation with Japan's Pharmaceutical and Medical Device Agency (PMDA) on the next steps for the submission for registration of its lead therapeutic asset, BCDA-01, for the treatment of ischemic heart failure of reduced ejection fraction (HFrEF).
加利福尼亞州陽光谷,2024年12月04日 (全球新聞)-- biocardia,公司[納斯達克:BCDA],全球領先的心血管和肺部疾病細胞及電芯衍生療法公司,今天宣佈與日本藥品和醫療器械管理局(PMDA)成功完成諮詢,討論提交其主要治療項目BCDA-01註冊的下一步,BCDA-01用於治療缺血性心力衰竭(HFrEF)。
"This most recent meeting with PMDA had several important outcomes," said Peter Altman, Ph.D., BioCardia's President and Chief Executive Officer." First, PMDA has invited our next consultation after the submission of our final clinical data with two-year follow-up to review the sufficiency of evidence to support claims of safety and efficacy for the BCDA-01 program. Second, PMDA remains open to the results from the CardiAMP Heart Failure Trial and our previous trials being sufficient evidence for registering CardiAMP Cell Therapy System for patients with heart failure in Japan."
「此次與PMDA的最新會議有幾個重要成果,」biocardia總裁兼首席執行官彼得·阿爾特曼博士表示。「首先,PMDA已邀請我們在提交最終臨床數據及兩年跟蹤之後進行下一次諮詢,以審查支持BCDA-01項目安全性和有效性聲明的證據是否充足。其次,PMDA仍然開放認爲,CardiAMP心力衰竭試驗及我們之前試驗的結果足以爲在日本註冊CardiAMP電芯療法系統的心力衰竭患者提供證據。」
Dr. Altman continued, "We are working on data lock from our fully enrolled 125 patient CardiAMP Heart Failure Trial and anticipate final data will be available in the first quarter of 2025."
阿爾特曼博士繼續說道,「我們正在處理125名患者的CardiAMP心力衰竭試驗的數據封鎖,並預計最終數據將在2025年第一季度可用。」
CardiAMP Cell Therapy for the treatment of HFrEF (BCDA-01) has received Breakthrough Designation from Food and Drug Administration Center for Biological Evaluation and Research (FDA CBER), with development supported by the Maryland Stem Cell Research Fund. All CardiAMP Cell Therapy clinical trials in the United States (BCDA-01 and BCDA-02) are also supported by reimbursement from the Center for Medicaid and Medicare Services (CMS).
CardiAMP電芯療法(BCDA-01)已獲得食品和藥物管理局生物評價與研究中心(FDA CBER)的突破性設計ations,開發得到了馬里蘭州幹細胞研究基金的支持。所有CardiAMP電芯療法在美國的臨床試驗(BCDA-01和BCDA-02)同樣得到了康哲藥業(CMS)的報銷支持。
About BioCardia:
關於biocardia:
BioCardia, Inc., headquartered in Sunnyvale, California, is a global leader in cellular and cell-derived therapeutics for the treatment of cardiovascular and pulmonary disease. CardiAMP autologous and CardiALLO allogeneic cell therapies are the Company's biotherapeutic platforms with three clinical stage product candidates in development. These therapies are enabled by its Helix biotherapeutic delivery and Morph vascular navigation product platforms. For more information visit: .
BioCardia公司總部位於加利福尼亞州的陽光谷,是治療心血管和肺部疾病的細胞和細胞衍生療法的全球領導者。CardiAMP自體細胞和CardiALLO異體細胞療法是公司的生物治療平台,目前正在開發三個臨床階段的產品候選者。這些療法得益於其Helix生物治療輸送和Morph血管導航產品平台。欲了解更多信息,請訪問:。
Forward Looking Statements:
前瞻性陳述:
This press release contains forward-looking statements that are subject to many risks and uncertainties. Forward-looking statements include, among other things, references to the Company's investigational product candidates, the timing of data lock on the CardiAMP Heart Failure Trial, the timing of availability of data from this trial, and future consultations with Japan PMDA. These forward-looking statements are made as of the date of this press release, and BioCardia assumes no obligation to update the forward-looking statements.
本新聞稿包含前瞻性聲明,這些聲明受到許多風險和不確定性的影響。前瞻性聲明包括公司研發產品候選者的相關內容、CardiAMP心力衰竭試驗的數據鎖定時間、該試驗數據的可用時間以及與日本PMDA的未來諮詢。這些前瞻性聲明是在本新聞稿發佈之日作出的,BioCardia不承擔更新前瞻性聲明的義務。
We may use terms such as "believes," "estimates," "anticipates," "expects," "plans," "intends," "may," "could," "might," "will," "should," "approximately" or other words that convey the uncertainty of future events or outcomes to identify these forward-looking statements. Although we believe that we have a reasonable basis for each forward-looking statement contained herein, we caution you that forward-looking statements are not guarantees of future performance and that our actual results may differ materially from the forward-looking statements contained in this press release. As a result of these factors, we cannot assure you that the forward-looking statements in this press release will prove to be accurate. Additional factors that could materially affect actual results can be found in BioCardia's Form 10-K filed with the Securities and Exchange Commission on March 27, 2024, under the caption titled "Risk Factors" and in our subsequently filed Quarterly Reports on Form 10-Q. BioCardia expressly disclaims any intent or obligation to update these forward-looking statements, except as required by law.
我們可能會使用諸如「相信」、「估計」、「預期」、「期望」、「計劃」、「意圖」、「可能」、「可以」、「也許」、「將要」、「應該」、「大約」或其他傳達未來事件或結果不確定性的詞彙來識別這些前瞻性聲明。雖然我們相信我們爲本聲明中包含的每個前瞻性聲明提供了合理的基礎,但我們提醒您,前瞻性聲明並不能保證未來的業績,並且我們的實際結果可能與本新聞稿中包含的前瞻性聲明有顯著不同。由於這些因素,我們無法保證本新聞稿中的前瞻性聲明將被證明是準確的。可能會顯著影響實際結果的其他因素可以在BioCardia於2024年3月27日在證券交易委員會提交的10-K表格中找到,標題爲「風險因素」,以及我們隨後提交的10-Q季度報告。BioCardia明確聲明不承擔更新這些前瞻性聲明的意圖或義務,除非法律要求。
Media Contact:
Miranda Peto, Investor Relations
Email: mpeto@BioCardia.com
Phone: 650-226-0120
媒體聯繫人:
Miranda Peto,投資者關係
郵箱:mpeto@BioCardia.com
電話:650-226-0120
Investor Contact:
David McClung, Chief Financial Officer
Email: investors@BioCardia.com
Phone: 650-226-0120
投資者聯繫:
David McClung, 首席財務官
郵箱:investors@BioCardia.com
電話:650-226-0120
譯文內容由第三人軟體翻譯。