Stock Price
16.07
Daily Change
0.06 0.37%
Monthly
-4.52%
Yearly
-14.57%
Q4 Forecast
15.71

EPS Reference Time Actual Consensus Previous
2026-11-05 FY2026Q3 PM 0.13 0.23 -0.13
2026-08-05 FY2026Q2 PM 0.64 0.21 2.02
2026-05-06 FY2026Q1 PM 3.16 1.11 -3.42
2026-02-25 FY2025Q4 PM -3.58 -1.27 1.90
2025-11-03 FY2025Q3 PM -0.13 -0.6 0.62



Peers Price Chg Day Year Date
Daiichi Sankyo 2,852.50 -5.00 -0.18% -18.62% Nov/13
Acadia Pharmaceuticals 18.75 0.61 3.36% -21.94% Nov/13
Agios Pharmaceuticals 31.59 -0.17 -0.54% -27.63% Nov/13
Alnylam Pharmaceuticals 165.04 8.39 5.36% -63.26% Nov/13
Amgen 465.67 -1.39 -0.30% 38.29% Nov/13
Tectonic Therapeutic 21.14 0.10 0.48% 14.02% Nov/13
BioCryst Pharmaceuticals 7.61 -0.07 -0.91% 7.49% Nov/13
Biogen 253.40 2.92 1.17% 51.24% Nov/13
BioMarin Pharmaceutical 57.23 0.53 0.93% 4.57% Nov/13
Capricor Therapeutics 9.53 -0.71 -6.93% 70.18% Nov/13

Indexes Price Day Year Date
USND 25136 -229.82 -0.91% 9.76% Nov/13
US Index 2000 2790 -8.57 -0.31% 16.84% Nov/13

Sarepta Therapeutics traded at $16.07 this Friday November 13th, increasing $0.06 or 0.37 percent since the previous trading session. Looking back, over the last four weeks, Sarepta Therapeutics gained 4.52 percent. Over the last 12 months, its price fell by 14.57 percent. Looking ahead, we forecast Sarepta Therapeutics to be priced at 15.71 by the end of this quarter and at 14.67 in one year, according to Trading Economics global macro models projections and analysts expectations.

Sarepta Therapeutics, Inc. is a commercial-stage biopharmaceutical company. The Company is focused on the discovery and development of ribonucleic acid (RNA)-targeted therapeutics, gene therapy and other genetic therapeutic modalities for the treatment of rare diseases. It is developing therapeutic candidates for a range of diseases and disorders, including Duchenne muscular dystrophy (DMD), Limb-girdle muscular dystrophies (LGMDs) and other neuromuscular and central nervous system (CNS) related disorders. Its commercial products, EXONDYS 51 (eteplirsen) Injection, VYONDYS 53 (golodirsen) Injection and AMONDYS 45 (casimersen) Injection is for the treatment of DMD in patients, who have a confirmed mutation of the DMD gene that is amenable to exon 51, exon 53 and exon 45 skipping. It is also developing gene therapy programs for various forms of LGMDs. Its LGMD product candidate, SRP-9003, is designed to transfer a gene that codes for and restores beta-sarcoglycan protein.