Immix Biopharma to Host Conference Call for Investors, Analysts and Members of the Media
Immix Biopharma to Host Conference Call for Investors, Analysts and Members of the Media
- Company management will provide an update on positive new developments regarding CAR-T NXC-201 in relapsed/refractory AL Amyloidosis. Following management's formal remarks, there will be a question-and-answer session.
- 公司管理層將提供關於復發/難治性阿爾茨海默病中CAR-t NXC-201的積極新進展的更新。在管理層正式發言後,將進行問答環節。
- Conference Call to be held Tuesday, December 10, 2024 at 4:30 p.m. Eastern Time
- 電話會議將在2024年12月10日(星期二)東部時間下午4:30舉行
- Interested parties can attend the conference call via Zoom using the following link:
- 有興趣的各方可以通過以下鏈接使用Zoom參會:
LOS ANGELES, CA, Dec. 09, 2024 (GLOBE NEWSWIRE) -- Immix Biopharma, Inc. ("ImmixBio", "Company", "We" or "Us" or "IMMX"), a clinical-stage biopharmaceutical company developing cell therapies for AL Amyloidosis and select immune-mediated diseases, announced that it will hold a conference call for investors, analysts and members of the media on Tuesday, December 10, 2024 at 4:30 p.m. Eastern Time.
洛杉磯,加利福尼亞州,2024年12月09日(全球新聞網)-- Immix Biopharma, Inc.("ImmixBio", "公司", "我們"或"IMMX"),一家臨床階段的生物製藥公司,開發用於阿爾茨海默病和部分免疫介導疾病的電芯療法,宣佈將於2024年12月10日東部時間下午4:30舉行投資者、分析師和媒體成員的電話會議。
Company management will provide an update on positive new developments regarding CAR-T NXC-201 in relapsed/refractory AL Amyloidosis. Following management's formal remarks, there will be a question-and-answer session.
公司管理層將提供有關重發/難治性AL澱粉樣變病的CAR-t NXC-201正面新進展的更新。在管理層正式發言後,將進行問答環節。
Interested parties can attend the conference call via Zoom using the following link:
相關方可以通過以下鏈接使用Zoom參加電話會議:
About NXC-201
NXC-201 is a sterically-optimized BCMA-targeted chimeric antigen receptor T (CAR-T) cell therapy. Initial data from Phase 1b/2 ex-U.S. study NEXICART-1 has demonstrated robust clinical responses with no neurotoxicity of any kind in relapsed/refractory AL Amyloidosis.
關於NXC-201
NXC-201是一種空間優化的BCMA靶向嵌合抗原受體t(CAR-T)細胞療法。來自美國以外的1b/2期研究NEXICARt-1的初步數據顯示,在重發/難治性AL澱粉樣變病患者中,臨床反應良好,且沒有任何神經毒性。
NXC-201 is being studied in a comprehensive clinical development program for the treatment of patients with relapsed/refractory AL amyloidosis, with the potential to expand into select immune-mediated diseases. The NXC-201 NEXICART-2 (NCT06097832) U.S. clinical trial builds on a robust clinical dataset. NXC-201 has been awarded Orphan Drug Designation (ODD) in AL Amyloidosis by the US FDA and in the EU by the EMA.
NXC-201正在一個全面的臨床開發項目中研究,旨在治療重發/難治性AL澱粉樣變病患者,並有潛力擴展到選擇性的免疫介導疾病。NXC-201 NEXICARt-2(NCT06097832)美國臨床試驗建立在強大的臨床數據集基礎上。NXC-201已獲得美國FDA及歐盟EMA對AL澱粉樣變的孤兒藥資格(ODD)。
About AL Amyloidosis
AL amyloidosis is caused by abnormal plasma cells in the bone marrow, which produce misfolded amyloid proteins that build-up in the heart, kidney, liver, and other organs. This build-up causes progressive and widespread damage to multiple organs, including heart failure, and leads to high mortality rates.
關於AL澱粉樣變
AL澱粉樣變是由骨髓中的異常漿細胞引起的,這些細胞產生錯誤摺疊的澱粉樣蛋白,這些蛋白在心臟、腎臟、肝臟及其他器官中積聚。此積聚導致多臟器的逐步和廣泛損害,包括心力衰竭,並導致高死亡率。
The U.S. observed prevalence of relapsed/refractory AL Amyloidosis is estimated to be growing at 12% per year according to Staron, et al Blood Cancer Journal, to approximately 33,277 patients in 2024.
根據Staron等人在《血液癌症雜誌》中的報道,美國復發/難治性AL澱粉樣變的觀察到的患病率預計每年增長12%,到2024年約爲33,277名患者。
The Amyloidosis market was $3.6 billion in 2017, and is expected to reach $6 billion in 2025, according to Grand View Research.
根據Grand View Research,澱粉樣變市場在2017年達到36億美元,預計到2025年將達到60億美元。
About Immix Biopharma, Inc.
Immix Biopharma, Inc. (ImmixBio) (Nasdaq: IMMX) is a clinical-stage biopharmaceutical company developing cell therapies for AL Amyloidosis and select immune-mediated diseases. Our lead candidate is sterically-optimized BCMA-targeted chimeric antigen receptor T (CAR-T) cell therapy NXC-201. NXC-201 is being evaluated in the U.S. Phase 1b/2 trial NEXICART-2 (NCT06097832) as well as the ex-U.S. study NEXICART-1 (NCT04720313). NXC-201 has demonstrated no neurotoxicity of any kind in AL Amyloidosis and short duration of cytokine release syndrome (CRS), supporting expansion into select immune-mediated diseases. NXC-201 has been awarded Orphan Drug Designation (ODD) in AL Amyloidosis by the US FDA and in the EU by the EMA. Learn more at and .
關於Immix Biopharma公司
Immix Biopharma, Inc.(ImmixBio)(納斯達克:IMMX)是一家臨床階段生物製藥公司,正在開發針對AL澱粉樣變性和特定免疫介導疾病的細胞治療。我們的主要候選藥物是空間優化BCMA靶向嵌合抗原受體T細胞療法NXC-201。NXC-201正在美國進行1b/2期臨床試驗NEXICARt-2(NCT06097832)以及在美國以外的NEXICARt-1研究(NCT04720313)。NXC-201在AL澱粉樣變性中未顯示任何類型的神經毒性,並且細胞因子釋放綜合症(CRS)持續時間短,支持向特定免疫介導疾病的擴展。NXC-201已獲得美國FDA和歐洲EMA對AL澱粉樣變性孤兒藥資格的認定。更多信息請訪問和。
Forward Looking Statements
This press release contains forward-looking statements regarding Immix Biopharma, Inc., its results of operations, prospects, future business plans and operations and the matters discussed above, including, but not limited to, the receipt of, timing of receipt, finalization of the terms of, and allocation of funds in connection with, the grant discussed above and potential benefits of our product candidate CAR-T NXC-201. These statements involve risks and uncertainties, and actual results may differ materially from any future results expressed or implied by the forward-looking statements. Forward-looking statements also include, but are not limited to, our plans, objectives, expectations and intentions and other statements that contain words such as "expects", "contemplates", "anticipates", "plans", "intends", "believes", "estimates", "potential", and variations of such words or similar expressions that convey the uncertainty of future events or outcomes, or that do not relate to historical matters. Those forward-looking statements involve known and unknown risks, uncertainties and other factors that could cause actual results to differ materially. Among those factors are: (i) the risk that the further data from the ongoing Phase 1b/2 clinical trials for CAR-T NXC-201 will not be favorably consistent with the initial data initial data readouts, (ii) the risk that the Company may not be able to advance to registration-enabling studies for CAR-T NXC-201 or other product candidates, (iii) that success in early phases of pre-clinical and clinicals trials do not ensure later clinical trials will be successful; (iv) that no drug product developed by the Company has received FDA pre-market approval or otherwise been incorporated into a commercial drug product, (v) the risk that the Company may not be able to obtain additional working capital with which to continue the clinical trials for CAR-T NXC-201, or advance to the initiation of registration-enabling studies, for such product candidates as and when needed and (vii) those other risks disclosed in the section "Risk Factors" included in the Company's Annual Report on Form 10-K filed with the SEC on March 29, 2024 and other periodic reports subsequently filed with the Securities and Exchange Commission. These reports are available at www.sec.gov. Immix Biopharma cautions that the foregoing list of important factors is not complete. Immix Biopharma cautions readers not to place undue reliance on any forward-looking statements. Immix Biopharma does not undertake, and specifically disclaims, any obligation to update or revise such statements to reflect new circumstances or unanticipated events as they occur, except as required by law. If we update one or more forward-looking statements, no inference should be drawn that we will make additional updates with respect to those or other forward-looking statements.
前瞻性聲明
本新聞稿包含關於Immix Biopharma, Inc.及其運營結果、前景、未來業務計劃和操作以及上述討論事項的前瞻性陳述,包括但不限於與上述討論的撥款相關的接收、接收時間、條款的最終確定和資金的分配,以及我們產品候選藥物CAR-t NXC-201的潛在益處。這些陳述涉及風險和不確定性,實際結果可能與任何前瞻性陳述所表達或暗示的未來結果存在重大差異。前瞻性陳述還包括但不限於我們的計劃、目標、期望和意圖,以及其他包含「期望」、「考慮」、「預期」、「計劃」、「打算」、「相信」、「估計」、「潛力」和這些詞的變體或類似表達的陳述,這些表達傳達了未來事件或結果的不確定性,或者與歷史事項無關。那些前瞻性陳述涉及已知和未知的風險、不確定性和其他因素,這些因素可能導致實際結果存在重大差異。在這些因素中包括:(i) 進一步的數據來自CAR-t NXC-201正在進行的1b/2期臨床試驗可能與初步數據讀數不一致的風險;(ii) 公司可能無法推進CAR-t NXC-201或其他產品候選藥物的註冊支持研究的風險;(iii) 早期臨床和前臨床試驗的成功並不保證後續臨床試驗會成功;(iv) 該公司開發的無藥物產品未獲得FDA的上市前批准或以其他方式被納入商業藥物產品;(v) 公司可能無法獲得額外的流動資金以繼續CAR-t NXC-201的臨床試驗或推進註冊支持研究所需的產品候選藥物的風險;(vii) 其他在公司於2024年3月29日向SEC提交的10-K表格的「風險因素」部分中披露的風險,以及隨後的其他定期報告。這些報告可在www.sec.gov上獲取。Immix Biopharma提醒,以上重要因素的列表並不完整。Immix Biopharma提醒讀者不要對任何前瞻性陳述寄予過多的信任。Immix Biopharma不承擔特別聲明的任何義務,並明確否認更新或修訂這些聲明以反映新情況或不可預見事件的義務,除非法律要求。如果我們更新一項或多項前瞻性陳述,不應推斷我們將對這些或其他前瞻性陳述進行額外更新。
Contacts
Mike Moyer
LifeSci Advisors
mmoyer@lifesciadvisors.com
聯繫人
邁克·莫耶
LifeSci顧問
mmoyer@lifesciadvisors.com
Company Contact
irteam@immixbio.com
公司聯繫人
irteam@immixbio.com
譯文內容由第三人軟體翻譯。