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Capricor Therapeutics and Parent Project Muscular Dystrophy to Host Webinar to Provide Recent Updates on CAP-1002 Program

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Capricor Therapeutics (NASDAQ: CAPR) will present 18-month data from its ongoing HOPE-2 open-label trial for CAP-1002, targeting Duchenne muscular dystrophy (DMD). The webinar is scheduled for January 25, 2023, at 1:00 p.m. ET, in collaboration with Parent Project Muscular Dystrophy (PPMD). CAP-1002 is a cardiac-derived cell therapy currently in late-stage clinical trials for DMD treatment. This presentation aims to share significant findings and ongoing research developments. A replay will be available on PPMD's website. For further details, visit www.parentprojectmd.org.

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-Company to present 18-month data results from ongoing HOPE-2 open label extension trial of CAP-1002 in patients with Duchenne muscular dystrophy-

-Webinar to be held on Wednesday, January 25, 2023 at 1:00 p.m. ET-

SAN DIEGO, Jan. 19, 2023 (GLOBE NEWSWIRE) -- Capricor Therapeutics (NASDAQ: CAPR) a biotechnology company focused on the development of transformative cell and exosome-based therapeutics for the treatment and prevention of muscular and other select diseases, announced today that the Company will present 18-month data results from its ongoing HOPE-2 open-label extension study with lead asset CAP-1002 for treating Duchenne muscular dystrophy (DMD). These recent updates will be presented on a webinar, hosted with the nonprofit organization, Parent Project Muscular Dystrophy (PPMD), on Wednesday, January 25, 2023 at 1:00 p.m. ET.

To listen to the webinar, please click the following link: http://join.parentprojectmd.org/webinar.

For additional details on the webinar, please visit www.parentprojectmd.org. A replay of the webinar will be made available on PPMD’s website.

About Capricor Therapeutics

Capricor Therapeutics, Inc. (NASDAQ: CAPR) biotechnology company focused on the development of transformative cell and exosome-based therapeutics for the treatment and prevention of muscular and other select diseases. Capricor’s lead candidate, CAP-1002, is an allogeneic cardiac-derived cell therapy that is currently in late-stage clinical development for treating Duchenne muscular dystrophy. Capricor is also developing its exosome technology as a next-generation therapeutic platform. The Company’s current focus is on developing exosomes capable of delivering nucleic acids, including mRNA, as well as proteins to treat or prevent a variety of diseases. For more information, visit capricor.com, and follow the Company on FacebookInstagram and Twitter.

Cautionary Note Regarding Forward-Looking Statements

Statements in this press release regarding the efficacy, safety, and intended utilization of Capricor’s product candidates; the initiation, conduct, size, timing and results of discovery efforts and clinical trials; the pace of enrollment of clinical trials; plans regarding regulatory filings, future research and clinical trials; regulatory developments involving products, including the ability to obtain regulatory approvals or otherwise bring products to market; the ability to achieve product milestones and to receive milestone payments from commercial partners; plans regarding current and future collaborative activities and the ownership of commercial rights; scope, duration, validity and enforceability of intellectual property rights; future royalty streams and revenue projections; expectations with respect to the expected use of proceeds from the recently completed offerings and the anticipated effects of the offerings; and any other statements about Capricor’s management team’s future expectations, beliefs, goals, plans or prospects constitute forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Any statements that are not statements of historical fact (including statements containing the words “believes,” “plans,” “could,” “anticipates,” “expects,” “estimates,” “should,” “target,” “will,” “would” and similar expressions) should also be considered to be forward-looking statements. There are a number of important factors that could cause actual results or events to differ materially from those indicated by such forward-looking statements. More information about these and other risks that may impact Capricor’s business is set forth in Capricor’s Annual Report on Form 10-K for the year ended December 31, 2021, as filed with the Securities and Exchange Commission on March 11, 2022 and in our Quarterly Report on Form 10-Q for the quarter ended September 30, 2022 as filed with the Securities and Exchange Commission on November 10, 2022. All forward-looking statements in this press release are based on information available to Capricor as of the date hereof, and Capricor assumes no obligation to update these forward-looking statements.

CAP-1002 is an Investigational New Drug and is not approved for any indications. None of Capricor’s exosome-based candidates have been approved for clinical investigation.

For more information, please contact:

Capricor Media Contact:
Raquel Cona
KCSA Strategic Communications
rcona@kcsa.com
212.896.1204

Capricor Investor Contact:
Joyce Allaire
LifeSci Advisors, LLC
jallaire@lifesciadvisors.com
617.435.6602

Capricor Company Contact:
AJ Bergmann, Chief Financial Officer
abergmann@capricor.com
310.358.3200


FAQ

What are the details of the Capricor webinar on CAP-1002?

The webinar will take place on January 25, 2023, at 1:00 p.m. ET, presenting 18-month data from the HOPE-2 trial for CAP-1002.

What is CAP-1002's indication and development status?

CAP-1002 is being developed as a treatment for Duchenne muscular dystrophy and is currently in late-stage clinical trials.

How can I access the CAP-1002 webinar?

You can listen to the webinar by visiting the Parent Project Muscular Dystrophy website on January 25, 2023.

Who is hosting the Capricor webinar?

The webinar is hosted in collaboration with Parent Project Muscular Dystrophy (PPMD).

What is Capricor Therapeutics focused on?

Capricor Therapeutics focuses on developing cell and exosome-based therapeutics for muscular and other select diseases.

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