Breakdown | TTM | Jun 2024 | Jun 2023 | Jun 2022 | Jun 2021 | Jun 2020 |
---|---|---|---|---|---|---|
Income Statement | ||||||
Total Revenue | 40.88K | 94.95K | 301.12K | 1.54M | 663.32K | 0.00 |
Gross Profit | -285.19K | 10.28K | -3.22M | -5.72M | -39.16K | -275.05K |
EBITDA | -3.98M | -36.44M | -6.87M | -12.83M | -9.18M | -7.71M |
Net Income | -4.84M | -36.57M | -5.57M | -11.95M | -8.55M | -7.02M |
Balance Sheet | ||||||
Total Assets | 2.39M | 5.18M | 33.89M | 37.70M | 39.37M | 35.79M |
Cash, Cash Equivalents and Short-Term Investments | 38.19K | 586.16K | 146.21K | 2.75M | 4.97M | 1.70M |
Total Debt | 6.30M | 5.95M | 437.90K | 500.91K | 551.08K | 632.32K |
Total Liabilities | 10.36M | 9.36M | 2.18M | 2.01M | 1.54M | 1.24M |
Stockholders Equity | -8.40M | -4.51M | 31.80M | 35.20M | 37.83M | 34.55M |
Cash Flow | ||||||
Free Cash Flow | -5.29M | -4.39M | -7.25M | -9.43M | -8.62M | -6.95M |
Operating Cash Flow | -5.29M | -4.39M | -7.25M | -9.43M | -8.62M | -6.94M |
Investing Cash Flow | 919.74K | 919.74K | 2.83M | -207.78K | 1.38M | 1.11M |
Financing Cash Flow | 4.36M | 3.92M | 1.77M | 7.10M | 10.53M | 4.50M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
57 Neutral | AU$6.84M | 60.67 | 2.14% | ― | ― | ― | |
54 Neutral | AU$43.23M | 17.07 | 26.99% | ― | ― | 51.85% | |
49 Neutral | AU$2.49B | 4.37 | -64.25% | 2.83% | 36.51% | 13.14% | |
46 Neutral | AU$2.68M | ― | -392.18% | ― | ― | 34.26% | |
46 Neutral | AU$11.11M | ― | -64.72% | ― | 139.19% | 33.33% | |
40 Underperform | AU$5.23M | ― | -263.02% | ― | -85.34% | 86.74% |
Zelira Therapeutics announced the publication of a clinical study demonstrating the efficacy and safety of its proprietary cannabinoid-based therapy, ZLT-L-007, in treating diabetic neuropathy. The study showed that ZLT-L-007 significantly outperformed Lyrica® (Pregabalin) in reducing pain and improving quality of life for patients, marking a potential shift in the standard-of-care treatment for diabetic neuropathy. The study, conducted under rigorous clinical standards, reported no serious adverse events, suggesting a promising future for ZLT-L-007 in the market.
Zelira Therapeutics has enhanced its financial flexibility by receiving a $1.15 million R&D Tax Incentive refund and establishing a $1 million At-the-Market funding facility. These financial moves support its ongoing development programs, including preparations for the FDA clinical trial of HOPE® 1. The company also completed the full conversion of US$3.25 million convertible notes into equity, strengthening its capital structure. The development of capsule formulations for HOPE® and Zenivol® using Zyraydi™ technology is on track for completion in mid to late 2025, aligning with Zelira’s strategy to enhance product consistency and market readiness.
Zelira Therapeutics has announced the full conversion of $USD3.25 million in Convertible Notes into equity within its HOPE® 1 SPV, which supports the clinical and regulatory development of treatments for Autism Spectrum Disorder. This conversion aligns investor interests, eliminates debt obligations, and strengthens the SPV’s capital structure, positioning it well for future institutional capital raises. The company has made significant progress in its clinical trial program, having completed a Pre-IND meeting with the U.S. FDA, which confirmed the appropriateness of targeting Phelan-McDermid Syndrome, a rare subset of Autism, for study. Zelira is now focused on submitting an IND to the FDA, initiating Phase 1 clinical trials, and filing for Orphan Drug Designation to leverage regulatory incentives.