Nippon Shinyaku and Capricor Therapeutics Enter into an Exclusive Partnership for Commercialization and Distribution of CAP-1002 for the Treatment* of Duchenne Muscular Dystrophy in US
Nippon Shinyaku Co., Ltd. and Capricor Therapeutics have formed an exclusive distribution agreement for CAP-1002, aimed at treating Duchenne muscular dystrophy (DMD) in the U.S. This investigational therapy is not yet approved in the U.S. CAP-1002 uses human cardiosphere-derived cells, targeting a range of DMD patients. A Phase II trial showed promise in enhancing upper limb and cardiac functions. The drug has received orphan and RMAT designations from the FDA, paving the way for a Phase III trial, with a potential market launch post-BLA approval.
- Exclusive agreement for distributions of CAP-1002 increases market potential in DMD treatment.
- Phase II study results indicate improved motor and cardiac functions in non-ambulatory DMD patients.
- Received orphan drug and RMAT designations from the FDA, facilitating priority review and accelerated approval.
- None.
KYOTO, Japan, Jan. 25, 2022 /PRNewswire/ -- *NS Pharma Note: CAP-1002 is an investigational therapy and not approved in the US.
This press release is being provided for a US audience as a reference. The original news release was issued by Nippon Shinyaku Co., Ltd., the parent company of NS Pharma on January 25, 2022 (Japan standard time). Please click here (https://www.nippon-shinyaku.co.jp/english/index.php). The text contains content related to U.S. unapproved drugs and unapproved indications.
Nippon Shinyaku Co., Ltd. (Headquarters: Kyoto, Japan, President: Toru Nakai) announced today that Nippon Shinyaku and Capricor Therapeutics (Headquarters: California, USA, CEO: Linda Marbán, NASDAQ: CAPR) have entered into an exclusive distribution agreement for CAP-1002 for the treatment* of Duchenne muscular dystrophy (DMD) in the territory of US.
DMD is a progressive muscular dystrophy caused by a deficiency of the dystrophin protein leading to weakness of skeletal, cardiac, and pulmonary muscles. DMD has a variety of genotypic variants, and therapeutic agents have been developed for patients with DMD caused by specific genetic mutations, thus contributing to the fulfillment of unmet medical needs. However, treatment for DMD patients due to the other type of genetic mutations and treatment for relatively older, non-ambulant DMD patients is still unsatisfactory, and effective therapies are required to be developed.
CAP-1002 is comprised of human allogeneic cardiosphere-derived cells. Exosomes (extracellular vesicles) secreted by CAP-1002 are thought to be the mechanism of action of CAP-1002 and have been shown to reduce oxidative stress, inflammation, fibrosis, and increase myocyte generation, as well as improve motor and cardiac function. CAP-1002 is expected to be effective in a wide range of DMD patients, regardless of the type of genetic mutation, and a Phase II clinical trial (HOPE-2 study) suggested improved upper limb function and improved cardiac function in non-ambulatory DMD patients. CAP-1002 has received orphan drug designation and RMAT designation from the U.S. Food and Drug Administration (FDA) and Capricor is currently ready to initiate a Phase III clinical trial (HOPE-3 study) at several US health institutions. After the BLA approval in US, CAP-1002 will be marketed by our wholly owned subsidiary NS Pharma, Inc. (New Jersey, USA, President: Tsugio Tanaka).
Nippon Shinyaku is focusing on the field of intractable, rare disorders, and have commercialized our in-house developed DMD treatment, Viltepso® (an antisense exon skipping agent) in the US. Executing this agreement with Capricor, Nippon Shinyaku aims to contribute further to the treatment for patients suffering from DMD.
About exosomes
Exosomes (extracellular vesicles) are vesicles of about 30 to 150 nanometers in diameter surrounded by a lipid-doublet membrane that are secreted by cells. Exosomes were previously considered relating to the excretion of intracellular waste products, but in recent years, it has been discovered and well known that exosomes contain proteins and nucleic acids and act as important mediators of intercellular communication. Research and development of clinical applications, such as therapeutic, diagnostic, and DDS, using this function has been actively pursued.
About Orphan Drug Designation
The Orphan Drug Designation is provided for orphan drugs and biologics intended for the safe and effective treatment, diagnosis or prevention of rare diseases/disorders that affect fewer than 200,000 people in the US, or that affect more than 200,000 persons but are not expected to recover the costs of developing and marketing a treatment drug. With orphan drug designation, the FDA grants a seven-year market exclusivity and provides tax incentives to the orphan drugs and biologics.
About RMAT designation
RMAT (Regenerative Medicine Advanced Therapy) is an FDA-designated system for advanced regenerative medicine therapies targeted at developing serious diseases that have shown certain effect in clinical trials based on the 21st Century Treatment Act (21st Century Cures Act) in US. Companies with RMAT designations are given the opportunity for priority review and accelerated approval for the product.
About Nippon Shinyaku
Our mission is to help people lead healthier and happier lives. Through creating unique medicines that will bring hope to patients and families struggling with illness, we aim to be an organization trusted by the community. Please visit our website (https://www.nippon-shinyaku.co.jp/english/) for products or detailed information.
About Capricor Therapeutics
Capricor Therapeutics, Inc. (NASDAQ: CAPR) is a biotechnology company focused on developing transformative cell and exosome-based therapeutics and vaccines for treating and preventing a broad spectrum of diseases. Capricor is also developing its exosome technology as a next-generation therapeutic platform for the delivery of nucleic acids, including mRNA to treat or prevent a variety of diseases. For more information, visit https://www.capricor.com.
Contact
Corporate Communications Dept., Nippon Shinyaku Co., Ltd.
FAX: +81-75-321-9128
About VILTEPSO® (viltolarsen) injection
Indication
VILTEPSO is indicated for the treatment of Duchenne muscular dystrophy (DMD) in
patients who have a confirmed mutation of the DMD gene that is amenable to exon 53
skipping. This indication is approved under accelerated approval based on an increase
in dystrophin production in skeletal muscle observed in patients treated with VILTEPSO.
Continued approval for this indication may be contingent upon verification and
description of clinical benefit in a confirmatory trial.
Important Safety Information
In clinical studies, no patients experienced kidney toxicity during treatment with
VILTEPSO. However, kidney toxicity from drugs like VILTEPSO may be possible. Your
doctor may monitor the health of your kidneys before starting and during treatment with
VILTEPSO.
Common side effects include upper respiratory tract infection, injection site reaction,
cough, and fever.
For more information about VILTEPSO, see full Prescribing Information.
View original content:SOURCE NS Pharma
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