Breakdown | ||||
Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|
Income Statement | Total Revenue | |||
0.00 | 0.00 | 0.00 | 0.00 | 0.00 | Gross Profit |
0.00 | -2.46M | -3.35M | -1.09M | -700.00K | EBIT |
-343.89M | -242.16M | -170.96M | -150.03M | -58.65M | EBITDA |
-343.89M | -233.48M | -164.75M | -148.20M | -58.34M | Net Income Common Stockholders |
-317.42M | -235.94M | -165.24M | -149.28M | -58.74M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | |||
642.27M | 123.10M | 256.01M | 376.57M | 345.31M | Total Assets |
691.23M | 165.08M | 306.32M | 425.66M | 353.33M | Total Debt |
23.99M | 27.41M | 30.48M | 32.64M | 0.00 | Net Debt |
-411.46M | -94.21M | -141.66M | -168.19M | -300.85M | Total Liabilities |
61.40M | 73.79M | 53.96M | 57.47M | 10.97M | Stockholders Equity |
629.84M | 91.29M | 252.36M | 368.20M | 342.37M |
Cash Flow | Free Cash Flow | |||
-294.75M | -188.89M | -156.71M | -123.18M | -47.67M | Operating Cash Flow |
-292.37M | -188.16M | -153.65M | -119.56M | -46.51M | Investing Cash Flow |
-204.08M | 83.31M | 87.20M | -137.89M | -45.66M | Financing Cash Flow |
809.89M | 54.32M | 37.39M | 157.82M | 380.69M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
77 Outperform | $13.74B | 32.75 | 8.05% | ― | 17.35% | 151.40% | |
69 Neutral | $9.67B | 41.83 | 19.71% | ― | 52.97% | ― | |
64 Neutral | $128.40B | ― | -3.15% | ― | 11.64% | -114.72% | |
56 Neutral | $4.14B | ― | 33.08% | ― | -13.97% | 43.51% | |
49 Neutral | $5.12B | ― | -93.03% | ― | -10.48% | -18.79% | |
49 Neutral | $6.90B | -0.08 | -53.01% | 2.43% | 24.84% | -3.06% | |
41 Neutral | $1.30B | ― | -88.03% | ― | ― | 14.93% |
Dyne Therapeutics has reported promising clinical data from its Phase 1/2 ACHIEVE trial of DYNE-101, targeting myotonic dystrophy type 1 (DM1), showing significant improvements in disease biomarkers and functional endpoints. The company plans a global Registrational Expansion Cohort to support a U.S. Accelerated Approval submission in 2026, highlighting the potential of DYNE-101 to transform treatment paradigms for DM1. Additionally, in the DELIVER trial for DYNE-251, targeting Duchenne muscular dystrophy, the company revealed favorable safety data and plans to pursue accelerated approval pathways, with submissions expected early in 2026.