EPIRUS Biopharmaceuticals, Inc.

EPIRUS Biopharmaceuticals, Inc.

EPRSQ
EPIRUS Biopharmaceuticals, Inc.US flagOther OTC
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1,571.00Market Cap
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Capital Structure

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Working Capital

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Growth Rates

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Quarterly Revenue

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Quarterly Earnings Per Share

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Quarterly Dividends Per Share

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Company Description

APIChat
CEO
Jeff Kagy
Full Time Employees
73
Sector
Healthcare
Industry
Biotechnology
Address
699 Boylston Street Boston MA United States of America 02116
IPO Date
Nov 9, 2005
Business
EPIRUS Biopharmaceuticals, Inc. EPIRUS Biopharmaceuticals, Inc. (EPRSQ) is a biopharmaceutical company focused on the development and commercialization of biosimilar monoclonal antibodies targeting immuno-inflammatory diseases and related conditions. The company offers a pipeline of biosimilar product candidates, including BOW015 (infliximab, reference product Remicade), BOW050 (adalimumab, reference product Humira), BOW070 (tocilizumab, reference product Actemra), BOW080 (eculizumab, reference product Soliris), BOW090 (ustekinumab, reference product Stelara), and BOW100 (golimumab, reference product Simponi); these candidates address therapeutic areas such as rheumatoid arthritis, inflammatory bowel disease, psoriasis, and rare blood disorders. EPIRUS Biopharmaceuticals conducts research, development, clinical trials, and manufacturing of these cost-effective biologic alternatives, utilizing advanced biotechnology to replicate the structure and function of reference biologics, with operations serving customers worldwide. Founded in 2013 and headquartered in Boston, Massachusetts, the company targets patients and healthcare providers seeking affordable treatments for chronic inflammatory and autoimmune conditions. In recent years, EPIRUS Biopharmaceuticals has pursued strategic growth through partnerships with entities like Livzon Mabpharm Inc. and Polpharma S.A. to accelerate product development and expand market reach; it completed the acquisition of Bioceros Holding B.V. in 2015, adding preclinical candidates to its pipeline and enhancing in-house development capabilities. These initiatives support ongoing global Phase 3 studies and commercialization efforts outside the U.S., amid a shift toward biosimilars amid its current over-the-counter trading status.