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Jasper Therapeutics to Present at Cantor Fitzgerald’s The Future of Oncology Virtual Symposium

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Jasper Therapeutics, Inc. (NASDAQ: JSPR) announced its participation in the Cantor Fitzgerald The Future of Oncology Virtual Symposium from April 3-5, 2023. Senior Vice President Wendy Pang will join a panel discussion on April 5 at 1:00 PM ET, addressing novel mechanisms for hematological malignancies. Jasper is developing briquilimab, a monoclonal antibody targeting c-Kit (CD117) for conditions like chronic spontaneous urticaria and lower to intermediate risk myelodysplastic syndromes (MDS). The therapy has shown promising safety and efficacy in over 130 subjects, with implications for stem cell transplants in rare diseases.

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REDWOOD CITY, Calif., March 31, 2023 (GLOBE NEWSWIRE) -- Jasper Therapeutics, Inc. (NASDAQ: JSPR), a biotechnology company focused on development of briquilimab, a novel antibody therapy targeting c-Kit (CD117) to address diseases such as chronic spontaneous urticaria, lower to intermediate risk myelodysplastic syndromes (MDS) as well as novel stem cell transplant conditioning regimes, today announced that it will participate at the Cantor Fitzgerald The Future of Oncology Virtual Symposium, to be held from April 3-5, 2023 in a virtual format.

Wendy Pang, M.D., Ph.D., Jasper’s Senior Vice President, Research and Translational Medicine, will be participating in a panel titled, “Novel Mechanisms to Address Unmet Need in Hematological Malignancies/Disorders”, on Wednesday, April 5th at 1:00 PM ET. Details for the live and archived webcast will be posted on the Company’s Investor Events webpage.

About Jasper Therapeutics
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 myelodysplastic syndromes (MDS) and as a conditioning agent for stem cell transplants for rare diseases such as sickle cell disease (SCD), Fanconi anemia (FA) and severe combined immunodeficiency (SCID). To date, briquilimab has a demonstrated efficacy and safety profile in over 130 dosed subjects and healthy volunteers, with clinical outcomes as a conditioning agent in SCID, acute myeloid leukemia (AML), MDS, FA, and SCD. In addition, briquilimab is being advanced as a transformational non-genotoxic conditioning agent for gene therapy. For more information, please visit us at www.jaspertherapeutics.com.

Forward-Looking Statements
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 Jasper’s priority development programs, Jasper’s resources, and its plan for achieving near-term clinical milestones. 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. Actual events and circumstances are difficult or impossible to predict and will differ from assumptions. 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; risks relating to uncertainty regarding the regulatory pathway for Jasper’s product candidates; the risk that prior study results may not be replicated; 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 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, including the ongoing COVID-19 pandemic; 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. 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.

Contacts:

John Mullaly (investors)
LifeSci Advisors
617-429-3548
jmullaly@lifesciadvisors.com

Jeet Mahal (investors)
Jasper Therapeutics
650-549-1403
jmahal@jaspertherapeutics.com


FAQ

What is the date of Jasper Therapeutics' participation in the Cantor Fitzgerald Symposium?

Jasper Therapeutics will participate in the Cantor Fitzgerald The Future of Oncology Virtual Symposium from April 3-5, 2023.

Who from Jasper Therapeutics will speak at the Symposium?

Wendy Pang, M.D., Ph.D., Senior Vice President of Research and Translational Medicine, will speak at the event.

What is briquilimab developed by Jasper Therapeutics?

Briquilimab is a monoclonal antibody targeting c-Kit (CD117) used for chronic spontaneous urticaria and myelodysplastic syndromes.

What conditions does briquilimab target?

Briquilimab targets chronic spontaneous urticaria, lower to intermediate risk myelodysplastic syndromes, and serves as a conditioning agent for stem cell transplants.

How many subjects have been dosed with briquilimab so far?

Briquilimab has been administered to over 130 subjects and healthy volunteers.

Jasper Therapeutics, Inc.

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Biotechnology
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United States of America
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