Capricor Therapeutics Inc (CAPR)

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Capricor Therapeutics Reports Third Quarter 2018 Financial Results and Provides Corporate Update

November 13, 2018

To Host Conference Call and Webcast Today at 4:30 p.m. ET

LOS ANGELES, Nov. 13, 2018 (GLOBE NEWSWIRE) -- Capricor Therapeutics (NASDAQ: CAPR), a clinical-stage biotechnology company focused on the development of first-in-class biological therapeutics for the treatment of Duchenne muscular dystrophy and other rare disorders, today announced its financial results for the third quarter of 2018, which ended September 30, 2018, and provided a corporate update.

“Capricor continues its progress in the clinical development of our novel cell therapy, CAP-1002, to treat Duchenne muscular dystrophy, and we are moving forward with our exosome-based therapy, CAP-2003,” said Linda Marbán, Ph.D., Capricor CEO. “Our HOPE-2 clinical trial, which is testing the safety and efficacy of CAP-1002 in boys and young men in the advanced stages of Duchenne, is well underway with 11 sites recruiting participants and more sites expected to begin enrollment before the end of the year. Pre-clinical and clinical studies have shown that CAP-1002 is generally safe, well-tolerated and demonstrated significant and sustained signals of improvement in cardiac and skeletal muscle function in patients with Duchenne muscular dystrophy.”

Capricor has been granted RMAT and Orphan Drug Designation by the U.S. Food and Drug Administration (FDA) for CAP-1002. The company’s leaders and key opinion leaders in the Duchenne community are scheduled to meet with the FDA in December under Capricor’s RMAT designation to discuss milestones for development and commercialization of CAP-1002.

Capricor has entered into a collaboration with the U.S. Army Institute of Surgical Research (USAISR), which is studying the potential for CAP-2003 to address trauma-related injuries and conditions.

CAP-2003 is comprised of proprietary extracellular vesicles, including exosomes, which are derived from cardiosphere-derived cells. Exosomes are nano-sized, membrane-enclosed vesicles, that are secreted by cells and contain bioactive molecules, including proteins, RNAs and microRNAs. Exosomes act as messengers to regulate the functions of neighboring cells. Because of these unique capacities, researchers are increasingly viewing exosomes as both a potential therapeutic and a vehicle to deliver gene and other therapies to targeted tissues in the human body.

“We are pleased to see that the power of exosomes is beginning to be recognized by the academic and the biotech communities,” said Dr. Marbán. “Pre-clinical studies indicate CAP-2003 has potential as a treatment for diseases of inflammation and fibrosis, which may mean it can potentially serve as both a therapy for those diseases and as a delivery vehicle for gene and other therapies to treat those diseases.”

Third Quarter Highlights and Recent Clinical and Operational Developments

Eleven study sites have opened and enrollment is underway in the HOPE-2 clinical trial. It is a Phase II, randomized, double-blind, placebo-controlled study in patients in the later stages of Duchenne muscular dystrophy, a fatal genetic disease with few treatment options. Current plans are to open up to 15 study sites and enroll approximately 84 patients. HOPE-2 will evaluate the safety and efficacy of repeat doses of CAP-1002, which consists of allogeneic cardiosphere-derived cells, or CDCs. CAP-1002 has been shown to exert potent immunomodulatory activity and stimulate cellular regrowth.
Capricor announced it will be meeting with the FDA in December as part of the expedited review process CAP-1002 received under the RMAT designation, which the FDA granted to CAP-1002 in February 2018. The FDA grants the RMAT designation to regenerative medicine therapies intended to treat a serious condition and for which preliminary clinical evidence indicates a potential to address unmet medical needs for that condition.
At the Gordon Research Conference on Extracellular Vesicles in Newry, Maine in August, Capricor presented a poster on the mechanism of action and the immunomodulatory capacities of CAP-2003. The poster provided additional evidence that exosomes may be the active pharmaceutical ingredient in CAP-1002. The pre-clinical studies further elucidated Capricor’s progress in developing the exosomes which comprise CAP-2003 as an exciting new potential therapeutic for diseases of inflammation and fibrosis.
In October, Capricor presented a poster at the 2018 Cell & Gene Meeting on the Mesa in La Jolla, CA. The poster reported on a pre-clinical study that assessed the biological mechanisms of action of paracrine factors and exosomes secreted by CDCs, the active component of CAP-1002. The poster showed that growth factors released by CDCs are able to activate survival signals in treated cells. Capricor also reported that the exosomes were responsible for CAP-1002’s immunomodulatory effects.
In November, Capricor presented a poster at the Action Duchenne International Conference in Birmingham, UK. The poster reported on a pre-clinical study that found exosomes secreted by CDCs were effective in increasing exercise capabilities and muscle activity in a mouse model of Duchenne muscular dystrophy. The poster also reported that the exosomes secreted by the CDCs reduced muscle fibrosis, which causes a loss of muscle function in Duchenne patients, and the proliferation of activated T cells, which help govern the body’s immune response, in the Duchenne mouse model.
Capricor provided corporate updates at the BTIG Fall Biotechnology Conference in New York and at the American Society of Exosomes and Microvesicles Annual Meeting in October. In November, Capricor provided an update on its research and development of cell and exosome-based therapies for Duchenne muscular dystrophy and other rare diseases during the BIO-Europe® 24th Annual International Partnering Conference in Copenhagen, Denmark.
Anticipated Events and Milestones in Fourth Quarter of 2018

Meet with the FDA to discuss Capricor’s Duchenne program through the RMAT process.
Continue to add additional sites and enroll patients in the HOPE-2 clinical trial.
Continue to conduct pre-clinical research for CAP-2003 to treat various diseases of inflammation and fibrosis.
Continue to develop processes for manufacturing scale-up and technology transfer of CAP-1002.
Third Quarter Results

The Company reported a net loss of approximately $4.1 million, or $0.14 per share, for the third quarter of 2018, compared to a net loss of approximately $2.7 million, or $0.12 per share, for the third quarter of 2017.

As of September 30, 2018, the Company's cash, cash equivalents and marketable securities totaled approximately $10.4 million, compared to approximately $14.1 million on December 31, 2017. Additionally, in the third quarter of 2018, Capricor raised approximately $1.1 million in net proceeds at an average price of approximately $1.44 per share under its at-the-market offering program. Capricor believes that its current financial resources should be sufficient to fund its operations and meet its financial obligations into the second quarter of 2019 based on the Company's current projections.

Conference Call and Webcast

To participate in the conference call, please dial 866-717-4562 (domestic) or 210-874-7812 (international) and reference the access code: 4974294.

To participate via a webcast, please visit: https://edge.media-server.com/m6/p/msqxw8py. The webcast will be archived for approximately 30 days and will be available at http://capricor.com/news/events/.

About Capricor Therapeutics

Capricor Therapeutics, Inc. (NASDAQ: CAPR) is a clinical-stage biotechnology company focused on the discovery, development and commercialization of first-in-class biological therapeutics for the treatment of rare disorders. Capricor’s lead candidate, CAP-1002, is an allogeneic cell therapy that is currently in clinical development for the treatment of Duchenne muscular dystrophy. Capricor has also established itself as one of the leading companies investigating the field of extracellular vesicles and is exploring the potential of CAP-2003, a cell-free, exosome-based candidate, to treat a variety of disorders. The HOPE-Duchenne trial was funded in part by the California Institute for Regenerative Medicine. For more information, visit www.capricor.com.

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