Breakdown | ||||
Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|
Income Statement | Total Revenue | |||
63.52M | 377.71M | 60.92M | 51.84M | 24.00K |
Gross Profit | ||||
63.52M | -59.67M | 38.34M | 35.40M | -103.16M |
EBIT | ||||
-415.57M | -176.49M | -338.48M | -392.46M | -132.76M |
EBITDA | ||||
-415.57M | -156.47M | -324.33M | -392.46M | -128.03M |
Net Income Common Stockholders | ||||
-376.74M | -132.53M | -263.59M | -341.36M | -256.42M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | |||
850.74M | 1.19B | 1.08B | 965.65M | 299.67M |
Total Assets | ||||
1.10B | 1.46B | 1.34B | 1.47B | 451.68M |
Total Debt | ||||
161.43M | 172.69M | 179.00M | 142.35M | 100.23M |
Net Debt | ||||
-120.54M | -263.21M | -53.76M | -823.30M | -61.94M |
Total Liabilities | ||||
370.28M | 478.38M | 608.24M | 647.72M | 206.12M |
Stockholders Equity | ||||
733.54M | 981.33M | 733.47M | 826.74M | 245.56M |
Cash Flow | Free Cash Flow | |||
-356.19M | -182.93M | -26.42M | -113.08M | -112.10M |
Operating Cash Flow | ||||
-347.25M | -149.19M | 22.53M | -66.27M | -95.74M |
Investing Cash Flow | ||||
185.01M | 71.84M | -461.34M | -294.14M | -100.12M |
Financing Cash Flow | ||||
7.74M | 276.45M | 111.59M | 756.14M | 322.32M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
48 Neutral | $6.36B | 1.28 | -45.04% | 2.64% | 19.24% | 1.69% | |
47 Neutral | $308.49M | ― | 181.41% | ― | 8001.47% | -37.69% | |
41 Neutral | $732.90M | ― | -54.00% | ― | 59.55% | 3.09% | |
39 Underperform | $1.63B | ― | -43.94% | ― | -83.18% | -144.95% | |
37 Underperform | $2.53B | ― | -74.17% | ― | ― | -43.10% | |
35 Underperform | $808.75M | ― | -78.34% | ― | ― | -70.45% |
On March 10, 2025, Beam Therapeutics announced positive initial data from its Phase 1/2 trial of BEAM-302 for treating alpha-1 antitrypsin deficiency (AATD). The trial demonstrated that BEAM-302, a liver-targeting lipid-nanoparticle formulation, was well tolerated and showed dose-dependent increases in functional AAT levels and decreases in mutant Z-AAT levels. This marks the first clinical genetic correction of a disease-causing mutation, offering potential treatment for both lung and liver disease in AATD patients. The company plans further dose escalation and expects to present more data in the second half of 2025.
Beam Therapeutics announced advancements in its base editing portfolio with key milestones anticipated in 2025. This progress is expected to bolster its industry positioning by advancing clinical programs, which aim to deliver life-long, curative genetic medicines, potentially impacting stakeholders through enhanced therapeutic options and financial stability.