Breakdown | ||||
Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 | Dec 2019 |
---|---|---|---|---|
Income Statement | Total Revenue | |||
56.60M | 54.09M | 76.88M | 35.00M | 173.44M | Gross Profit |
25.99M | -24.69M | 39.17M | -23.50M | 124.28M | EBIT |
-306.81M | -262.82M | -195.90M | -156.43M | -36.44M | EBITDA |
-126.09M | -284.50M | -169.35M | -181.94M | -73.64M | Net Income Common Stockholders |
-144.72M | -366.71M | -202.14M | -262.05M | -155.50M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | |||
2.30B | 2.48B | 2.50B | 2.71B | 2.99B | Total Assets |
2.49B | 2.66B | 2.83B | 3.07B | 3.43B | Total Debt |
8.42M | 4.24M | 2.75M | 1.59M | 3.81M | Net Debt |
-321.70M | -2.47B | -2.49B | -2.71B | -2.99B | Total Liabilities |
148.94M | 117.16M | 100.89M | 85.42M | 102.17M | Stockholders Equity |
2.34B | 2.54B | 2.73B | 2.98B | 3.32B |
Cash Flow | Free Cash Flow | |||
-163.32M | -156.85M | -154.13M | -123.87M | -102.57M | Operating Cash Flow |
-144.16M | -142.45M | -146.93M | -84.91M | -74.34M | Investing Cash Flow |
149.84M | -1.30B | -274.49M | 132.30M | 602.27M | Financing Cash Flow |
-81.50M | -1.42M | -31.10M | -21.67M | -48.22M |
Ascletis Pharma Inc. has announced its 2025 Annual General Meeting, scheduled for May 22, 2025, in Hangzhou, China. The meeting will address several key business items, including the consideration of the company’s audited financial statements for 2024, the re-election of directors, and the re-appointment of KPMG as the auditor. Additionally, resolutions will be proposed to authorize the company’s board to manage share allotments and repurchases, potentially impacting the company’s capital structure and shareholder value.
Ascletis Pharma Inc. announced positive results from its Phase Ib study of ASC30, a small molecule oral GLP-1 receptor agonist, which showed significant body weight reduction in participants with obesity. The study supports a ‘lower starting dose and slower titration’ strategy for the upcoming Phase IIa study, which has been submitted to the FDA, indicating potential advancements in obesity treatment and reinforcing Ascletis’s position in the pharmaceutical industry.
Ascletis Pharma Inc. announced positive interim results from its U.S. Phase Ib trial of ASC30, a potentially first-in-class subcutaneous injection small molecule GLP-1R agonist. The trial demonstrated a 36-day half-life for one formulation, supporting less frequent administration, and showed a favorable safety profile with no serious adverse events. This advancement could enhance Ascletis’ positioning in the obesity treatment market, offering a novel therapeutic option with both oral and injectable formulations.
Ascletis Pharma Inc. announced its annual results for 2024, revealing a significant increase in R&D expenses due to its focus on developing treatments for obesity and metabolic diseases. Despite a substantial loss for the year, the company has sufficient cash reserves to support its operations and R&D activities until 2029, highlighting its commitment to advancing its pipeline and maintaining a competitive edge in the biomedical industry.
Ascletis Pharma Inc. announced positive results from its Phase Ib studies of ASC47, a weight loss drug candidate, demonstrating a significant half-life and good tolerability in both healthy subjects and patients with obesity. The U.S. FDA has cleared the IND application for ASC47 in combination with semaglutide, potentially enhancing the company’s positioning in the obesity treatment market by offering a promising new therapy option.
Ascletis Pharma Inc. announced positive interim results from its U.S. Phase Ib study of the ASC30 oral tablet, showing significant mean body weight reductions in patients with obesity. The ASC30 tablet was well tolerated, with no serious adverse events reported, enhancing its potential as a promising treatment for obesity. This advancement strengthens Ascletis’s position in the pharmaceutical industry and could have significant implications for stakeholders and the obesity treatment market.