Breakdown | ||||
Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|
Income Statement | Total Revenue | |||
210.78M | 129.01M | 0.00 | 0.00 | 0.00 | Gross Profit |
210.78M | 29.13M | -1.90M | -1.12M | -326.00K | EBIT |
47.01M | -3.16M | -97.25M | -51.13M | -26.67M | EBITDA |
47.01M | -321.00K | -95.35M | -50.01M | -26.34M | Net Income Common Stockholders |
65.63M | -6.68M | -87.46M | -50.07M | -26.38M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | |||
420.00M | 351.97M | 45.16M | 291.06M | 39.05M | Total Assets |
526.32M | 469.19M | 252.06M | 305.83M | 43.53M | Total Debt |
59.21M | 68.23M | 25.94M | 0.00 | 0.00 | Net Debt |
-42.00M | 628.00K | -19.22M | -291.06M | -39.05M | Total Liabilities |
97.64M | 226.83M | 39.50M | 7.12M | 85.02M | Stockholders Equity |
428.68M | 242.36M | 212.55M | 298.72M | -41.49M |
Cash Flow | Free Cash Flow | |||
-44.72M | 134.19M | -96.67M | -55.44M | -27.89M | Operating Cash Flow |
-41.56M | 139.80M | -93.79M | -50.86M | -25.57M | Investing Cash Flow |
-27.80M | -138.40M | -148.65M | -4.58M | -2.32M | Financing Cash Flow |
102.96M | 21.04M | 479.00K | 307.46M | 50.09M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
69 Neutral | $9.77B | 41.86 | 19.71% | ― | 52.97% | ― | |
64 Neutral | $400.38M | 5.59 | 19.56% | ― | 63.38% | ― | |
51 Neutral | $1.60B | ― | -73.24% | ― | -4.42% | -42.17% | |
49 Neutral | $6.90B | 0.02 | -54.05% | 2.46% | 24.91% | -3.14% | |
48 Neutral | $13.03B | ― | -28.77% | ― | -52.75% | 25.00% | |
47 Neutral | $2.07B | ― | -600.68% | ― | -98.62% | -86.21% | |
36 Underperform | $3.56B | ― | -33.47% | ― | 13.99% | 0.17% |
On February 24, 2025, Entrada Therapeutics announced that the FDA has lifted the clinical hold on ENTR-601-44, granting authorization for a Phase 1b clinical study of the drug aimed at treating Duchenne muscular dystrophy (DMD) in adult patients. This significant regulatory milestone allows Entrada to initiate its ELEVATE-44-102 study in the U.S. and expand its global clinical program, potentially positioning the company as a leader in developing therapies for DMD.
On February 3, 2025, Entrada Therapeutics announced receiving authorization from the UK’s Medicines and Healthcare Products Regulatory Agency to initiate a Phase 1/2 clinical trial of ENTR-601-44 for Duchenne muscular dystrophy. This trial, set to start in the second quarter of 2025, aims to evaluate the safety, tolerability, and efficacy of ENTR-601-44 in patients amenable to exon 44 skipping, marking a significant step in addressing the medical needs of this patient population with limited treatment options.