{"id":943543,"date":"2026-03-11T09:32:09","date_gmt":"2026-03-11T13:32:09","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/tempest-announces-partnership-for-tpst-2003-in-preparation-for-planned-u-s-registrational-study-in-2026\/"},"modified":"2026-03-11T09:32:09","modified_gmt":"2026-03-11T13:32:09","slug":"tempest-announces-partnership-for-tpst-2003-in-preparation-for-planned-u-s-registrational-study-in-2026","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/tempest-announces-partnership-for-tpst-2003-in-preparation-for-planned-u-s-registrational-study-in-2026\/","title":{"rendered":"Tempest Announces Partnership for TPST-2003 in Preparation for Planned U.S. Registrational Study in 2026"},"content":{"rendered":"<div class=\"mw_release\">\n<ul type=\"disc\">\n<li style=\"margin-bottom:6pt;text-align:justify\">\n          <em>Cincinnati Children\u2019s Applied Gene and Cell Therapy Center selected to conduct tech transfer, development and IND-enabling manufacturing<\/em>\n        <\/li>\n<li style=\"margin-bottom:6pt\">\n          <em>All activities other than long-term stability testing planned to be complete in Q3 2026 to support potential IND filing in Q4 2026<\/em>\n        <\/li>\n<li style=\"margin-bottom:6pt\">\n          <em>Selection of tech transfer partner follows Tempest\u2019s recent announcement of positive interim data from the ongoing REDEEM-1 Phase 1\/2a trial of TPST-2003, including 100% CR in all six efficacy evaluable patients, and accelerated development timeline<\/em><br \/>\n          \n        <\/li>\n<\/ul>\n<p align=\"justify\">BRISBANE, Calif., March  11, 2026  (GLOBE NEWSWIRE) &#8212; Tempest Therapeutics, Inc. (Nasdaq: TPST) (\u201cTempest\u201d), a clinical-stage biotechnology company developing a pipeline of advanced CAR-T cell therapy product candidates to treat cancer, today announced the selection of Cincinnati Children\u2019s Applied Gene and Cell Therapy Center (\u201cAGCTC\u201d) as the lead contract development and manufacturing partner to conduct the formal technology transfer of TPST-2003, Tempest\u2019s dual-targeting CD19\/BCMA CAR-T therapy under development for the treatment of relapsed\/refractory multiple myeloma (\u201crrMM\u201d).<\/p>\n<p align=\"justify\">Tempest recently announced that, as of a January 31, 2026 data cutoff, a total of 36 patients with rrMM had received one infusion of TPST-2003, including 24 patients in a prior Phase 1\/2 investigator-initiated trial (IIT) and 12 patients in the ongoing REDEEM-1 trial, representing one of the largest datasets evaluating a CD19\/BCMA dual-targeting CAR-T therapy. As of the data cutoff, all six efficacy evaluable patients enrolled in the REDEEM-1 trial had achieved a complete response (CR) according to the International Myeloma Working Group (IMWG) uniform response criteria. Among 25 evaluable patients with measurable disease at baseline across both studies, the overall response rate (\u201cORR\u201d) was 100% (25\/25). Tempest plans to present the results of the REDEEM-1 trial and updated results from the IIT at a scientific meeting later this year.<\/p>\n<p align=\"justify\">\u201cThe recent positive results from the ongoing REDEEM-1 trial position TPST-2003 as a potential class-leading therapy for rrMM, which, subject to FDA approval, could offer a meaningful option for patients with rrMM,\u201d said Dr. Matt Angel, President and Chief Executive Officer of Tempest. \u201cThe potential to treat patients with extramedullary disease (EMD) and patients who have previously received a BCMA-targeting CAR-T is particularly exciting. We are very pleased to have selected the AGCTC as our partner to execute the technology transfer of TPST-2003 as we prepare for our planned U.S. clinical development.\u201d<\/p>\n<p align=\"justify\">The AGCTC is a research, development, and manufacturing hub advancing future cell and gene therapy (CGT) treatments for patients with unmet needs. Established in 2001, the center has evolved into a nationally recognized leader in CTG CDMO services with a proven track record that reflects Cincinnati Children\u2019s commitment to solving unmet medical needs through translational science. AGCTC is part of the Cincinnati Children\u2019s Cancer and Blood Diseases Institute, which is ranked #1 in the nation by U.S. News &amp; World Report for pediatric cancer care.<\/p>\n<p align=\"justify\">\u201cWe are proud to have been selected to support the development of this exciting product candidate,\u201d said Dr. Chaozhong Zou, Executive Director and General Manager of AGCTC, Cancer and Blood Diseases Institute, Cincinnati Children\u2019s Hospital Medical Center. \u201cThe parallel-structure dual-targeting CAR architecture of TPST-2003 is truly innovative, and fits perfectly within our experience supporting technology transfer of engineered cell therapy products, including our extensive experience making novel CAR-T programs IND-ready. We look forward to generating the information needed to advance TPST-2003 to the next stage of development.\u201d<\/p>\n<p align=\"justify\">\n        <strong>About TPST-2003<\/strong>\n      <\/p>\n<p align=\"justify\">TPST-2003 is an autologous CD19\/BCMA dual-targeting CAR-T therapy designed to improve response depth and durability in patients with relapsed\/refractory multiple myeloma (rrMM) through a parallel dual-targeting CAR structure designed to address tumor heterogeneity and antigen escape. TPST-2003 is being developed in China by Tempest\u2019s partner, Novatim Immune Therapeutics (\u201cNovatim\u201d). Under its agreement with Novatim, Tempest has the exclusive right to develop TPST-2003 outside of China, India, Turkey, and Russia.<\/p>\n<p align=\"justify\">\n        <strong>About REDEEM-1<\/strong>\n      <\/p>\n<p align=\"justify\">REDEEM-1 (Study nos. CTR20233309\/NCT06223646) is a Phase 1\/2a clinical trial evaluating TPST-2003 in patients with relapsed\/refractory multiple myeloma, including patients with high-risk cytogenetics and patients with extramedullary disease. The REDEEM-1 trial has a targeted full enrollment of 29 patients. The REDEEM-1 trial is sponsored and being conducted by Tempest\u2019s partner, Novatim Immune Therapeutics, with a total of eight clinical sites registered in China: Peking Union Medical College Hospital (Dr. Jian Li; lead site), The First Affiliated Hospital of Nanchang University (Dr. Fei Li), Peking University First Hospital (Dr. Yujin Dong), Henan Cancer Hospital (Dr. Baijun Fang), Shanxi Provincial Cancer Hospital (Dr. Liping Su), The Second Xiangya Hospital of Central South University (Dr. Hongling Peng), The First Affiliated Hospital of China Medical University (Dr. Xiaojing Yan), and The Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College (Dr. Dehui Zou).<\/p>\n<p align=\"justify\">\n        <strong>Additional clinical trials evaluating TPST-2003<\/strong>\n      <\/p>\n<p align=\"justify\">A Phase 1\/2 IIT (Study no. NCT04714827) is evaluating TPST-2003 in patients with relapsed\/refractory multiple myeloma, including patients with high-risk cytogenetics and patients with extramedullary disease. The IIT is sponsored and being conducted by Tempest\u2019s partner, Novatim Immune Therapeutics, with a total of two clinical sites registered in China: Shanghai Fourth People\u2019s Hospital (Dr. Weijun Fu; lead site) and Shanxi Provincial Cancer Hospital (Dr. Liping Su).<\/p>\n<p align=\"justify\">A Phase 1 trial (Study nos. CTR20242409\/NCT06518876) is evaluating TPST-2003 in patients with POEMS, a rare blood disorder caused by abnormal plasma cells. The Phase 1 trial is sponsored and being conducted by Tempest\u2019s partner, Novatim Immune Therapeutics, with a total of three clinical sites registered in China: Peking Union Medical College Hospital (Dr. Jian Li; lead site), Xuanwu Hospital Capital Medical University (Dr. Wanling Sun), and West China Hospital, Sichuan University (Dr. Yu Wu).<\/p>\n<p>\n        <strong>About Tempest Therapeutics<\/strong>\n      <\/p>\n<p align=\"justify\">Tempest Therapeutics is a clinical-stage biotechnology company developing a pipeline of advanced CAR-T cell therapy product candidates to treat cancer. Tempest is headquartered in Brisbane, California. More information about Tempest can be found on the company\u2019s website at https:\/\/www.tempesttx.com.<\/p>\n<p>\n        <strong>Forward-Looking Statements <\/strong>\n      <\/p>\n<p align=\"justify\">This press release contains forward-looking statements (including within the meaning of Section 21E of the Securities Exchange Act of 1934, as amended, and Section 27A of the Securities Act of 1933, as amended (the \u201cSecurities Act\u201d)) concerning Tempest Therapeutics, Inc. These statements may discuss goals, intentions, and expectations as to future plans, trends, events, results of operations or financial condition, or otherwise, based on current beliefs of the management of Tempest Therapeutics, as well as assumptions made by, and information currently available to, management of Tempest Therapeutics. Forward-looking statements generally include statements that are predictive in nature and depend upon or refer to future events or conditions, and include words such as \u201cmay,\u201d \u201cwill,\u201d \u201cshould,\u201d \u201cwould,\u201d \u201ccould\u201d, \u201cexpect,\u201d \u201canticipate,\u201d \u201cplan,\u201d \u201clikely,\u201d \u201cbelieve,\u201d \u201cestimate,\u201d \u201cproject,\u201d \u201cintend,\u201d and other similar expressions. All statements that are not historical facts are forward-looking statements, including but not limited to, statements regarding: Tempest Therapeutics\u2019 plan to present data from clinical trials, including the REDEEM-1 trial; the design, initiation, progress, timing, scope and results of clinical trials, including the anticipated initiation of U.S. registrational trial for TPST-2003 in Q4 2026; the planned advancement of a diversified next-generation CAR-T pipeline; anticipated therapeutic benefit and regulatory development of Tempest Therapeutics\u2019 product candidates, including TPST-2003; and Tempest Therapeutics\u2019 ability to achieve its operational plans. Any forward-looking statements in this press release are based on Tempest Therapeutics\u2019 current expectations, estimates and projections about its industry as well as management\u2019s current beliefs and expectations of future events only as of today and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements. These risks and uncertainties include, but are not limited to Tempest Therapeutics\u2019 need for additional capital to fund its planned programs and operations and to continue to operate as a going concern; unexpected safety or efficacy data observed during preclinical or clinical trials; the possibility that results from prior clinical trials and preclinical studies may not necessarily be predictive of future results; past results may not be indicative of future results; clinical trial site activation or enrollment rates that are lower than expected; loss of key personnel; changes in expected or existing competition; changes in the regulatory environment; risks relating to volatility and uncertainty in the capital markets for biotechnology companies; and unexpected litigation or other disputes. These and other factors that may cause actual results to differ from those expressed or implied are discussed in greater detail in the \u201cRisk Factors\u201d section of Tempest\u2019s Quarterly Report on Form 10-Q for the quarter ended September 30, 2025, filed with the Securities and Exchange Commission (\u201cSEC\u201d) on November 5, 2025, and the \u201cRisk Factors\u201d section under Proposal 5 contained in Tempest\u2019s definitive proxy statement on Schedule 14A, filed with the SEC on December 31, 2025, and in other documents filed by Tempest from time to time with the SEC. Except as required by applicable law, Tempest Therapeutics undertakes no obligation to revise or update any forward-looking statement, or to make any other forward-looking statements, whether as a result of new information, future events or otherwise. These forward-looking statements should not be relied upon as representing Tempest Therapeutics\u2019 views as of any date subsequent to the date of this press release and should not be relied upon as prediction of future events. In light of the foregoing, investors are urged not to rely on any forward-looking statement in reaching any conclusion or making any investment decision about any securities of Tempest Therapeutics.<\/p>\n<p>\n        <strong>Investor Contacts:<\/strong>\n      <\/p>\n<p>Sylvia Wheeler<br \/>Wheelhouse Life Science Advisors<br \/><u><a href=\"https:\/\/www.globenewswire.com\/Tracker?data=LgTvQQiulmxStIaBnokx9DrQ7x1eRBYQU5AjYknTZXFcloAmbdCIYbLQaZDoNrjIgNeR1vUjhp2Wo_a_yO9kZMH2t6om-9AbgKUXBypuK25edNsV-5w36cxc55TOuEjQ\" rel=\"nofollow\" target=\"_blank\">swheeler@wheelhouselsa.com<\/a><\/u><\/p>\n<p>Aljanae Reynolds <br \/>Wheelhouse Life Science Advisors<br \/><u><a href=\"https:\/\/www.globenewswire.com\/Tracker?data=SKL5gKX_t6zDjNnz7A3FWkma4ngIc58zk8kqQB7uy0p-zQyBsTvaEqtJ06vShrstvhdmb0k-wLpDv-ZvnPxE9nVyWCNEcj7ZSJD1O2WchrYCMZh3lQ0S6dbl4xXJgYqG\" rel=\"nofollow\" target=\"_blank\">areynolds@wheelhouselsa.com<\/a><\/u><\/p>\n<p>      <img decoding=\"async\" alt=\"\" class=\"__GNW8366DE3E__IMG\" src=\"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=OTY2OTc4MiM3NDc5MTgzIzIxODk5MzQ=\" \/><br \/>\n      <br \/>\n      <img decoding=\"async\" alt=\"\" src=\"https:\/\/ml.globenewswire.com\/media\/ZjY0OWNlMjUtMzc4NS00YTA1LTlhOGEtZDc4ZDY2NDRlNjRkLTEyMDE0ODctMjAyNi0wMy0xMS1lbg==\/tiny\/Tempest-Therapeutics.png\" \/>\n    <\/div>\n<div class=\"mw_contactinfo\"><\/div>\n","protected":false},"excerpt":{"rendered":"<p>Cincinnati Children\u2019s Applied Gene and Cell Therapy Center selected to conduct tech transfer, development and IND-enabling manufacturing All activities other than long-term stability testing planned to be complete in Q3 2026 to support potential IND filing in Q4 2026 Selection of tech transfer partner follows Tempest\u2019s recent announcement of positive interim data from the ongoing REDEEM-1 Phase 1\/2a trial of TPST-2003, including 100% CR in all six efficacy evaluable patients, and accelerated development timeline BRISBANE, Calif., March 11, 2026 (GLOBE NEWSWIRE) &#8212; Tempest Therapeutics, Inc. (Nasdaq: TPST) (\u201cTempest\u201d), a clinical-stage biotechnology company developing a pipeline of advanced CAR-T cell therapy product candidates to treat cancer, today announced the selection of Cincinnati Children\u2019s Applied Gene and Cell Therapy Center (\u201cAGCTC\u201d) as &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/www.marketnewsdesk.com\/index.php\/tempest-announces-partnership-for-tpst-2003-in-preparation-for-planned-u-s-registrational-study-in-2026\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;Tempest Announces Partnership for TPST-2003 in Preparation for Planned U.S. Registrational Study in 2026&#8221;<\/span><\/a><\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[],"tags":[],"class_list":["post-943543","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.5 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Tempest Announces Partnership for TPST-2003 in Preparation for Planned U.S. Registrational Study in 2026 - Market Newsdesk<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.marketnewsdesk.com\/index.php\/tempest-announces-partnership-for-tpst-2003-in-preparation-for-planned-u-s-registrational-study-in-2026\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Tempest Announces Partnership for TPST-2003 in Preparation for Planned U.S. Registrational Study in 2026 - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"Cincinnati Children\u2019s Applied Gene and Cell Therapy Center selected to conduct tech transfer, development and IND-enabling manufacturing All activities other than long-term stability testing planned to be complete in Q3 2026 to support potential IND filing in Q4 2026 Selection of tech transfer partner follows Tempest\u2019s recent announcement of positive interim data from the ongoing REDEEM-1 Phase 1\/2a trial of TPST-2003, including 100% CR in all six efficacy evaluable patients, and accelerated development timeline BRISBANE, Calif., March 11, 2026 (GLOBE NEWSWIRE) &#8212; Tempest Therapeutics, Inc. (Nasdaq: TPST) (\u201cTempest\u201d), a clinical-stage biotechnology company developing a pipeline of advanced CAR-T cell therapy product candidates to treat cancer, today announced the selection of Cincinnati Children\u2019s Applied Gene and Cell Therapy Center (\u201cAGCTC\u201d) as &hellip; Continue reading &quot;Tempest Announces Partnership for TPST-2003 in Preparation for Planned U.S. Registrational Study in 2026&quot;\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.marketnewsdesk.com\/index.php\/tempest-announces-partnership-for-tpst-2003-in-preparation-for-planned-u-s-registrational-study-in-2026\/\" \/>\n<meta property=\"og:site_name\" content=\"Market Newsdesk\" \/>\n<meta property=\"article:published_time\" content=\"2026-03-11T13:32:09+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=OTY2OTc4MiM3NDc5MTgzIzIxODk5MzQ=\" \/>\n<meta name=\"author\" content=\"Newsdesk\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Newsdesk\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"8 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/tempest-announces-partnership-for-tpst-2003-in-preparation-for-planned-u-s-registrational-study-in-2026\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/tempest-announces-partnership-for-tpst-2003-in-preparation-for-planned-u-s-registrational-study-in-2026\\\/\"},\"author\":{\"name\":\"Newsdesk\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/#\\\/schema\\\/person\\\/482f27a394d4fda80ecb5499e519d979\"},\"headline\":\"Tempest Announces Partnership for TPST-2003 in Preparation for Planned U.S. Registrational Study in 2026\",\"datePublished\":\"2026-03-11T13:32:09+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/tempest-announces-partnership-for-tpst-2003-in-preparation-for-planned-u-s-registrational-study-in-2026\\\/\"},\"wordCount\":1578,\"image\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/tempest-announces-partnership-for-tpst-2003-in-preparation-for-planned-u-s-registrational-study-in-2026\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/www.globenewswire.com\\\/newsroom\\\/ti?nf=OTY2OTc4MiM3NDc5MTgzIzIxODk5MzQ=\",\"inLanguage\":\"en-US\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/tempest-announces-partnership-for-tpst-2003-in-preparation-for-planned-u-s-registrational-study-in-2026\\\/\",\"url\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/tempest-announces-partnership-for-tpst-2003-in-preparation-for-planned-u-s-registrational-study-in-2026\\\/\",\"name\":\"Tempest Announces Partnership for TPST-2003 in Preparation for Planned U.S. Registrational Study in 2026 - 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