Breakdown | |||||
TTM | Mar 2024 | Mar 2023 | Mar 2022 | Mar 2021 | Mar 2020 |
---|---|---|---|---|---|
Income Statement | Total Revenue | ||||
3.41M | 4.45M | 1.19M | 1.98M | 1.53M | 34.23K | Gross Profit |
3.01M | 4.01M | 1.12M | 1.98M | 1.53M | 33.42K | EBIT |
-6.10M | -4.42M | -7.48M | -5.63M | -3.88M | -2.26M | EBITDA |
-6.24M | -4.56M | -7.26M | -3.64M | -2.34M | -2.22M | Net Income Common Stockholders |
-6.19M | -4.50M | -6.24M | -3.64M | -2.28M | -2.22M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | ||||
3.20M | 3.39M | 9.26M | 14.61M | 1.85M | 1.11M | Total Assets |
5.03M | 14.85M | 18.68M | 24.48M | 10.88M | 9.12M | Total Debt |
0.00 | 1.59M | 2.27M | 2.10M | 0.00 | 0.00 | Net Debt |
-3.20M | -1.80M | -6.99M | -12.51M | -1.85M | -1.11M | Total Liabilities |
1.03M | 3.43M | 2.85M | 2.64M | 539.13K | 510.62K | Stockholders Equity |
4.00M | 11.42M | 15.84M | 21.85M | 10.34M | 8.61M |
Cash Flow | Free Cash Flow | ||||
-2.76M | -5.13M | -5.31M | -4.42M | ― | -2.09M | Operating Cash Flow |
-2.76M | -5.13M | -5.29M | -4.40M | -2.92M | -2.09M | Investing Cash Flow |
-2.62K | -2.23K | -58.42K | -26.64K | ― | 0.00 | Financing Cash Flow |
1.68M | -772.98K | -84.22K | 17.19M | 3.66M | 1.96M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
54 Neutral | AU$205.01M | ― | -37.20% | ― | ― | 32.02% | |
54 Neutral | $5.31B | 3.29 | -45.39% | 2.79% | 16.77% | -0.07% | |
51 Neutral | AU$68.68M | ― | -131.55% | ― | 12.53% | -11.04% | |
46 Neutral | AU$25.60M | ― | -41.60% | ― | ― | ― | |
43 Neutral | AU$38.41M | ― | -75.39% | ― | ― | 44.29% |
Amplia Therapeutics Ltd. presented interim data from its ACCENT trial at the AACR annual meeting, showcasing the promising efficacy of its FAK inhibitor, narmafotinib, in combination with chemotherapy for advanced pancreatic cancer. The data indicates that narmafotinib is well tolerated and shows better outcomes compared to chemotherapy alone, with a higher disease control rate and longer median duration on trial. This development could enhance Amplia’s positioning in the oncology market and provide new hope for stakeholders involved in pancreatic cancer treatment.
Amplia Therapeutics Limited has initiated trial activities for a new pancreatic cancer treatment in the US, combining their FAK inhibitor narmafotinib with the chemotherapy FOLFIRINOX. The trial, managed by a multinational CRO, aims to assess the safety, tolerability, and efficacy of this combination in advanced pancreatic cancer patients, potentially enhancing treatment outcomes and strengthening Amplia’s position in the oncology field.
Amplia Therapeutics has reported promising updated data from its ongoing ACCENT trial, which is evaluating the FAK inhibitor narmafotinib in combination with chemotherapy for advanced pancreatic cancer. The trial has shown encouraging efficacy with 13 confirmed partial responses and good tolerability, suggesting that narmafotinib may enhance the effectiveness of chemotherapy. This data will be presented at the American Association of Cancer Research Annual Meeting, highlighting the drug’s potential impact on pancreatic cancer treatment and reinforcing Amplia’s position in the oncology sector.
Amplia Therapeutics announced a positive outcome from its Type D meeting with the FDA regarding its planned clinical trial in the US for narmafotinib, a FAK inhibitor, in combination with FOLFIRINOX for advanced pancreatic cancer. The FDA’s approval of the proposed changes to the trial protocol allows Amplia to proceed with final planning stages, potentially positioning narmafotinib as a preferred drug in combination therapies for pancreatic cancer, enhancing its market position and offering promising prospects for stakeholders.
Amplia Therapeutics Limited has announced a change in the exercise prices of its unlisted options following a successful A$13 million capital raising completed in December 2024. The adjustments, set to take effect on February 20, 2025, are in line with ASX Listing Rule 6.22.2 and will involve distributing replacement holding statements and application forms to all option holders, potentially impacting stakeholder engagement and financial strategies.