Sarepta Therapeutics, Inc. Share Price & Technical Analysis

SRPT · $16.80 (-0.94%)

Healthcare / Biotechnology

AI Score 20 · Bearish

$16.80

-0.94%

Sarepta Therapeutics, Inc., a commercial-stage biopharmaceutical company, focuses on the discovery and development of RNA-targeted therapeutics, siRNA platform, gene therapy, and other genetic therapeutic modalities for the treatment of rare diseases. It offers EXONDYS 51 for the treatment of Duchenne in patients who have a confirmed mutation of the dystrophin gene that is amenable to exon 51 skip

Price chart

Seasonality

May has 3 positive and 2 negative years (last 5 years shown)

-20% return in May, -12% avg return in past 3 year May month.

-14% return in 2026, -37% avg return in past 3 years.

Swipe sideways to see all months →

JanFebMarAprMayJunJulAugSepOctNovDecYr
26-7%-16%34%-5%-20%-14%
25-7%-4%-40%-3%-40%-55%-4%13%7%27%-12%3%-116%
2425%7%2%-2%2%23%-10%-5%-8%1%6%-8%32%
23-3%-2%-4%-10%1%-7%-5%12%0%-44%19%19%-26%
22-21%7%3%-8%1%3%25%18%1%3%7%6%46%

Monthly return % by calendar month · historical pattern, not a forecast

AI snapshotScore 20/100

Bearish · Downtrend · Weak

Sarepta Therapeutics, Inc., a commercial-stage biopharmaceutical company, focuses on the discovery and development of RNA-targeted therapeutics, siRNA platform, gene therapy, and other genetic therapeutic modalities for the treatment of rare diseases. It offers EXONDYS 51 for the treatment of Duchenne in patients who have a confirmed mutation of the dystrophin gene that is amenable to exon 51 skipping; VYONDYS 53 for the treatment of Duchenne in patients who have a confirmed mutation of the dystrophin gene that is amenable to exon 53 skipping; AMONDYS 45 for the treatment of Duchenne in patients who have a confirmed mutation of the dystrophin gene that is amenable to exon 45 skipping; and ELEVIDYS, an AAV-based gene therapy, which is contraindicated in patients with any deletion in exon 8 and/or exon 9 in the Duchenne gene. The company also develops SRP-9003, a gene therapy program for the treatment of LGMD2E; SRP-1001 to selectively target and knockdown DUX4 using RNAi in Phase 1/2a clinical trials; and SRP-1003 for reduction of expression of the DMPK gene in Phase 1/2a clinical trials. It has collaboration and license agreements with F. Hoffman-La Roche Ltd; Arrowhead Pharmaceuticals, Inc.; University of Western Australia; Nationwide Children's Hospital; Hansa Biopharma; and Duke University. The company was incorporated in 1980 and is headquartered in Cambridge, Massachusetts.

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Key metrics

Market cap

$2.00B

P/E ratio

54.11

52W high

$43.92

52W low

$10.42

Volume

19,59,125

Beta

0.26

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