| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 55.70M | 63.52M | 377.71M | 60.92M | 51.84M | 24.00K |
| Gross Profit | -356.09M | -304.04M | 377.71M | -250.67M | -180.29M | -103.16M |
| EBITDA | -430.13M | -393.64M | -146.95M | -324.33M | -230.06M | -128.03M |
| Net Income | -414.64M | -376.74M | -132.53M | -289.09M | -370.64M | -194.59M |
Balance Sheet | ||||||
| Total Assets | 1.31B | 1.10B | 1.46B | 1.34B | 1.47B | 451.68M |
| Cash, Cash Equivalents and Short-Term Investments | 1.07B | 850.74M | 1.19B | 1.08B | 965.65M | 299.67M |
| Total Debt | 151.42M | 161.43M | 172.69M | 179.00M | 147.64M | 107.64M |
| Total Liabilities | 345.08M | 370.28M | 478.38M | 608.24M | 647.72M | 206.12M |
| Stockholders Equity | 966.00M | 733.54M | 981.33M | 733.47M | 826.74M | 245.56M |
Cash Flow | ||||||
| Free Cash Flow | -352.36M | -356.19M | -182.93M | -26.42M | -113.08M | -112.10M |
| Operating Cash Flow | -338.18M | -347.25M | -149.19M | 22.53M | -66.27M | -95.74M |
| Investing Cash Flow | -103.56M | 185.01M | 71.84M | -461.34M | -294.14M | -100.12M |
| Financing Cash Flow | 479.61M | 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 |
|---|---|---|---|---|---|---|---|
60 Neutral | $3.72B | ― | -28.17% | ― | 129.21% | 80.35% | |
59 Neutral | $1.99B | ― | -7.52% | ― | 27.51% | 38.72% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
45 Neutral | $2.64B | ― | -44.44% | ― | ― | -5.30% | |
45 Neutral | $4.23B | ― | -95.93% | ― | ― | -27.70% | |
44 Neutral | $2.44B | -5.42 | -47.19% | ― | -84.07% | -157.71% | |
43 Neutral | $3.52B | ― | -34.78% | ― | ― | -34.96% |
Beam Therapeutics, Inc., a biotechnology company based in Cambridge, Massachusetts, focuses on developing precision genetic medicines through its base editing technology to provide life-long cures for genetic diseases. The company operates in the biotechnology sector and is committed to advancing its portfolio of programs and maintaining a strong intellectual property position.
Study Overview: Beam Therapeutics, Inc. is conducting a Phase 1/2 study titled ‘A Phase 1/2 Dose-exploration and Dose-expansion Study to Evaluate the Safety and Efficacy of BEAM-302 in Adult Patients With Alpha-1 Antitrypsin Deficiency (AATD)-Associated Lung Disease and/or Liver Disease.’ The study aims to assess the safety, tolerability, pharmacokinetics/pharmacodynamics (PK/PD), and efficacy of BEAM-302, as well as to determine the optimal biological dose (OBD) for treating AATD-associated conditions.
Beam Therapeutics, Inc. is conducting a Phase 1/2 study titled A Phase 1/2, Dose-Exploration Study to Evaluate the Safety and Efficacy of BEAM-301 in Patients With Glycogen Storage Disease Type Ia (GSDIa). This study aims to assess the safety, tolerability, and efficacy of BEAM-301, a novel treatment for patients with GSDIa who have specific genetic variants. The study’s significance lies in its potential to offer a new therapeutic option for this rare metabolic disorder.
Beam Therapeutics, Inc. is conducting the BEACON trial, officially titled ‘A Phase 1/2 Study Evaluating the Safety and Efficacy of a Single Dose of Autologous CD34+ Base Edited Hematopoietic Stem Cells (BEAM-101) in Patients With Sickle Cell Disease and Severe Vaso-Occlusive Crises.’ The study aims to assess the safety and efficacy of BEAM-101 in treating severe sickle cell disease, a condition with significant health impacts. This trial holds potential significance for advancing treatment options for this debilitating disease.