Sarepta Therapeutics

Sarepta Therapeutics

The Leader in RNA-based Medicine | Sarepta Therapeutics.

HQ location
Cambridge, United States
Launch date
Market cap
$1.8b
Enterprise value
$2.3b
Share price
$18.07 SRPT
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$700m

Post IPO Convertible
Total Funding000k

Financials

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Revenues, earnings & profits over time
USD2018201920202021202220232024
Revenues0000000000000000000000000000
% growth95 %27 %42 %30 %33 %33 %53 %
EBITDA0000000000000000000000000000
% EBITDA margin(105 %)(123 %)(98 %)(59 %)(51 %)(3 %)17 %
Profit0000000000000000000000000000
% profit margin(120 %)(188 %)(103 %)(60 %)(75 %)(43 %)12 %
EV0000000000000000000000000000
EV / revenue00.0x00.0x00.0x00.0x00.0x00.0x00.0x
EV / EBITDA00.0x00.0x00.0x00.0x00.0x00.0x00.0x
R&D budget0000000000000000000000000000
R&D % of revenue133 %147 %134 %110 %94 %71 %42 %

Source: Company filings or news article

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More about Sarepta Therapeutics
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Sarepta Therapeutics is a global biotechnology company focused on developing precision genetic medicines to treat rare diseases that significantly impact lives. The company has established a strong position in the treatment of Duchenne muscular dystrophy (DMD) and is advancing gene therapies for limb-girdle muscular dystrophy (LGMD), Charcot-Marie-Tooth (CMT) disease, MPS IIIA, and other central nervous system (CNS) disorders. Sarepta operates in the biopharmaceutical market, targeting patients with rare genetic conditions that have limited treatment options. The company's business model revolves around research and development (R&D) of innovative therapies, progressing them through clinical trials, and obtaining regulatory approvals to bring these treatments to market. Revenue is primarily generated through the sale of approved therapies and strategic partnerships. Sarepta's mission is to expedite the drug development process, reducing the time from laboratory research to patient treatment, and to build the largest gene therapy manufacturing capacity to meet global demand.

Keywords: biotechnology, genetic medicine, rare diseases, Duchenne muscular dystrophy, gene therapy, limb-girdle muscular dystrophy, Charcot-Marie-Tooth, CNS disorders, clinical trials, biopharmaceutical.

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Investments by Sarepta Therapeutics

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Eisai
ACQUISITION by Sarepta Therapeutics Jul 2014
Myonexus Therapeutics
ACQUISITION by Sarepta Therapeutics Feb 2019
StrideBio
ACQUISITION by Ginkgo Bioworks Apr 2023
AavantiBio
ACQUISITION by Solid Biosciences Sep 2022