Sarepta Therapeutics,, Inc. Common Stock (SRPT) Stock Price
SRPTStock
$17.10−26.74%52W
Market Cap$1.81B
P/E7.77x
PEG Ratio-0.09
Div yield—
Beta0.47
SRPT Share Price Chart
Favorite Metrics
Price vs S&P 500 (26W)-32.70%
Price vs S&P 500 (4W)-13.77%
PEG Ratio-0.09
VGM Score53.14
P/E Ratio (Annual)7.77x
SRPT Earnings Surprise History
| Quarter | Report date | EPS estimate | EPS actual | Surprise |
|---|---|---|---|---|
| Q2 2026 | $0.49 | $0.64 | +31.67%(+$0.15) | |
| Q1 2026 | $1.05 | $3.16 | +202.07%(+$2.11) | |
| Q4 2025 | -$0.77 | -$3.58 | -365.29%(-$2.81) | |
| Q3 2025 | -$0.37 | -$0.13 | +65.03%(+$0.24) | |
| Q2 2025 | $1.16 | $2.02 | +73.90%(+$0.86) |
SRPT Analyst Recommendations
Jun 2026
Jul 2026
Aug 2026
Sep 2026
3.42
3.38
3.45
3.45
Industry Peers — Pharmaceuticals(574)
| Symbol | Value Score | Growth Score | Momentum Score | P/S Ratio (TTM) | Revenue Growth TTM (YoY) | Gross Margin (TTM) | EPS Growth (5Y) | Price |
|---|---|---|---|---|---|---|---|---|
SRPTSarepta Therapeutics,, Inc. Common Stock | C | C | B | 0.9x | -20.4% | 67.5% | — | $17.10 |
| LLYEli Lilly & Co. | D | B | A | 14.9x | 49.6% | 83.4% | 27.6% | $1257.03 |
| JNJJohnson & Johnson | D | C | B | 6.2x | 7.8% | 67.7% | 14.9% | $255.56 |
| ABBVABBVIE INC. | D | C | A | 7.8x | 10.4% | 72.8% | -2.9% | $285.42 |
| MRKMerck & Co., Inc. | D | C | A | 5.4x | 4.6% | 77.3% | 21.2% | $145.95 |
| NVSNovartis AG | C | C | B | 4.9x | 3.3% | 75.0% | 15.3% | $150.62 |
| AZNAstraZeneca PLC | C | B | B | 4.3x | 8.6% | 81.3% | 21.9% | $165.41 |
| ABTAbbott Laboratories | C | C | B | 3.9x | 8.1% | 56.8% | 8.2% | $104.89 |
| NVONovo-Nordisk A/S | B | C | C | 3.5x | 5.6% | 80.7% | 20.7% | $38.83 |
| PFEPfizer Inc. | C | D | A | 2.6x | -0.2% | 74.7% | -3.5% | $29.58 |
| VRTXVertex Pharmaceuticals Inc | D | C | B | 10.1x | 10.2% | 86.0% | 8.3% | $499.74 |
About Sarepta Therapeutics,, Inc. Common Stock
Sarepta Therapeutics is a commercial-stage biopharmaceutical company specializing in RNA-targeted and gene therapies for rare neuromuscular disorders. The company has four FDA-approved treatments for Duchenne muscular dystrophy and maintains a pipeline of additional candidates for neuromuscular and other rare diseases. Its integrated business model encompasses discovery through patient delivery of genetic medicines for underserved patient populations.