Sarepta Therapeutics, Inc. (SRPT) 股票分析
医疗保健Sarepta Therapeutics, Inc.
$16.67
$-0.13 (-0.77%)
最后更新: 2026年5月26日
价格走势
暂无价格数据
分析
公司概述
Sarepta Therapeutics, Inc. operates as a commercial-stage biopharmaceutical enterprise dedicated to the discovery and development of RNA-targeted therapeutics, siRNA platforms, gene therapy, and other genetic therapeutic modalities specifically for treating rare diseases. The company primarily offers treatments such as EXONDYS 51 for Duchenne muscular dystrophy, positioning itself within the highly specialized healthcare sector and the broader biotechnology industry. Its operational scale is defined by a market capitalization of $2.30B, an annual revenue of $2.20B, and a workforce consisting of 835 employees. These valuation and revenue figures indicate that while the company maintains a significant market presence within the biotech landscape, its financial structure reflects the capital-intensive nature of genetic therapy development and commercialization.
财务健康
The company reported revenue of $2.20B and EBITDA of $-613,251,008 over the trailing twelve months, while net income stood at $-713,409,984. The substantial negative gap between revenue and net income reveals a cost structure characterized by heavy losses, likely driven by research and development expenses or commercialization costs that exceed gross profit generation, resulting in a gross margin of -7.4%. Despite these operating losses, the company generated free cash flow of $95.92M, which suggests a degree of financial flexibility allowing for continued investment in its therapeutic pipeline without immediate reliance on external equity financing. The operating margin of -92.6% and profit margin of -32.5% further underscore the current phase of business development where profitability has not yet been achieved. On the balance sheet, total cash holdings of $939.65M are contrasted against total debt of $1.04B, resulting in a debt-to-equity ratio of 91.14, which indicates a highly leveraged position relative to equity capitalization. However, the current ratio of 2.32 demonstrates strong short-term liquidity, implying that the company possesses sufficient current assets to cover its short-term obligations comfortably. Additionally, the return on equity of -53.5% and return on assets of -11.2% reveal that management has yet to generate positive returns on the capital invested in the business, a common characteristic for pre-revenue or early commercial-stage biotechnology firms.
估值评估
The valuation metrics present a complex picture, with a trailing P/E ratio of N/A due to negative earnings and a forward P/E of 7.20. The disparity between a non-existent trailing P/E and a forward P/E of 7.20 implies that the market is pricing in a significant expected earnings trajectory shift, anticipating future profitability despite current losses. The price-to-book ratio stands at 2.02, indicating that the market values the company at twice its book value, which suggests a premium assigned to its intangible assets, proprietary therapies, and future revenue potential. Alternative valuation measures include a price-to-sales ratio of 1.05 and an EV/EBITDA of -3.91, suggesting that the market is valuing the company primarily on revenue multiples rather than earnings multiples given the current loss position. The stock has traded within a 52-week range between $10.42 and $64.80, with the current valuation sitting significantly below the 52-week high, reflecting recent market volatility or sentiment shifts. The beta value of 0.28 indicates that the stock exhibits low price volatility relative to the broader market, moving less than half as much as the overall market index.
Growth & Income
The company experienced a revenue growth rate of -32.7% year-over-year, while earnings growth is listed as N/A due to the absence of prior period earnings for comparison. The negative revenue growth rate indicates a contraction in sales, which in the absence of positive earnings growth suggests that revenue declines are directly impacting the bottom line rather than being offset by margin expansion. As a non-dividend payer, the company maintains a dividend yield of N/A and a payout ratio of 0.0%, meaning that all generated cash is reinvested into growth initiatives such as drug development and commercial expansion rather than distributed to shareholders. This reinvestment strategy is typical for biotechnology firms seeking to capture value from future market approvals and pipeline progression. Overall, the growth and income profile is defined by significant revenue contraction and a complete absence of current income distribution, reflecting a capital-intensive growth stage where financial resources are prioritized for long-term therapeutic development over immediate shareholder returns.
同行比较
Sarepta Therapeutics, Inc. (SRPT) 在生物技术行业运营。以下是其与市值最接近的同行的比较:
| 公司 | 代码 | 市值 | 市盈率 |
|---|---|---|---|
| Sarepta Therapeutics, Inc. | SRPT | $1.76B | 47.6 |
| Vertex Pharmaceuticals Incorporated | VRTX | $110.64B | 25.8 |
| Regeneron Pharmaceuticals, Inc. | REGN | $66.98B | 15.6 |
| argenx SE | ARGX | $50.52B | 36.0 |
生物技术行业平均市盈率为53.8倍。Sarepta Therapeutics, Inc.的市盈率为47.6。
本分析由AI生成,仅供参考,不构成投资建议。数据可能存在延迟或不准确。在做出投资决策之前,请务必进行自己的研究并咨询合格的财务顾问。
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关于Sarepta Therapeutics, Inc.
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.
公司简介以英文显示。
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