Breakdown | |||||
TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|---|
Income Statement | Total Revenue | ||||
0.00 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | Gross Profit |
-265.58K | 0.00 | -445.55K | -440.00K | -267.20K | -225.23K | EBIT |
-21.88M | -31.84M | -41.13M | -24.18M | -6.87M | -5.22M | EBITDA |
-26.97M | -31.25M | -40.19M | -24.54M | -6.60M | -5.56M | Net Income Common Stockholders |
-28.14M | -32.19M | -39.00M | -24.54M | -7.02M | -5.41M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | ||||
1.21M | 6.01M | 19.81M | 49.78M | 27.87M | 3.95M | Total Assets |
3.08M | 7.53M | 22.11M | 52.48M | 29.82M | 5.73M | Total Debt |
546.47K | 569.94K | 136.12K | 275.98K | 393.35K | 702.61K | Net Debt |
-661.10K | -5.44M | -8.59M | -3.50M | -27.48M | -3.25M | Total Liabilities |
21.01M | 20.48M | 9.59M | 4.88M | 1.75M | 1.58M | Stockholders Equity |
-17.93M | -12.96M | 12.51M | 47.61M | 28.07M | 4.14M |
Cash Flow | Free Cash Flow | ||||
-19.47M | -18.90M | -30.44M | -14.75M | -6.86M | -4.94M | Operating Cash Flow |
-19.47M | -18.90M | -30.34M | -14.42M | -6.84M | -3.94M | Investing Cash Flow |
9.04M | 11.12M | 34.78M | -46.34M | -228.78K | 994.37K | Financing Cash Flow |
5.13M | 5.07M | 503.46K | 36.66M | 31.00M | 5.10M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
79 Outperform | C$72.38M | 13.73 | 19.57% | ― | 38.28% | ― | |
66 Neutral | C$50.69M | 25.35 | 6.85% | ― | 2.72% | -47.79% | |
53 Neutral | C$88.38M | ― | -149.09% | ― | ― | -67.03% | |
52 Neutral | $5.14B | 3.39 | -43.55% | 2.83% | 16.49% | -0.19% | |
33 Underperform | C$65.70M | ― | 248.46% | ― | ― | 32.71% | |
25 Underperform | C$62.94M | ― | ― | -32.14% | -52.38% |
Sernova Biotherapeutics has secured a $4 million loan from Navigate Private Yield Fund LP III to advance its clinical development plans, particularly for its Cell Pouch Bio-hybrid Organ aimed at treating type 1 diabetes. This funding, supported by a secured guarantee from the company’s U.S. subsidiary and a board member, will be used for working capital and corporate purposes, positioning Sernova as a leading company in U.S. clinical trials for implantable and retrievable diabetes treatment solutions.
Spark’s Take on TSE:SVA Stock
According to Spark, TipRanks’ AI Analyst, TSE:SVA is a Underperform.
Sernova Biotherapeutics faces critical financial challenges with no revenue and ongoing losses, posing a high-risk profile. Technical indicators suggest bearish trends, compounded by an unfavorable valuation. However, recent positive corporate developments, including clinical trial advancements, offer some potential for future growth. The stock remains high-risk and speculative.
To see Spark’s full report on TSE:SVA stock, click here.
Sernova Biotherapeutics announced that their Cell Pouch Bio-hybrid Organ, aimed at providing a functional cure for type 1 diabetes, will be featured at the 2025 Cell & Gene Meeting on the Med in Rome. This highlights the company’s collaboration with Evotec and the scientific community’s interest in their innovative approach, potentially impacting the treatment landscape for chronic diseases like diabetes.
Spark’s Take on TSE:SVA Stock
According to Spark, TipRanks’ AI Analyst, TSE:SVA is a Underperform.
Sernova faces significant financial risks with no revenue and ongoing losses. While technical indicators suggest bearish trends, recent corporate developments in clinical trials and leadership changes could offer some longer-term potential. However, the current financial distress overshadows these prospects, making the stock very high-risk.
To see Spark’s full report on TSE:SVA stock, click here.
Sernova Biotherapeutics has announced a positive update on its Phase 1/2 clinical trial for the Cell Pouch Bio-hybrid Organ aimed at treating type 1 diabetes. The Data and Safety Management Board has approved the enrollment of the final patient in Cohort B, and Sernova is preparing to advance to Cohort C in the second half of 2025. The trial’s primary endpoint is to demonstrate the safety and tolerability of islet transplantation into the Cell Pouch. The ongoing trial has shown promising results, including islet cell survival and insulin independence in patients, with no evidence of detrimental fibrosis. Sernova plans to collaborate with Evotec to launch a T1D trial using induced pluripotent stem cell islet-like clusters following the conclusion of Cohort C.
Sernova Biotherapeutics has appointed Dr. Pericles Calias as Chief Development Officer and Head of R&D to enhance its operational depth and expertise in cell therapy. Dr. Calias brings extensive experience in drug product development and regulatory approvals, which is expected to accelerate the advancement of Sernova’s Cell Pouch Bio-hybrid Organ as a functional cure for T1D, potentially transforming treatment paradigms and benefiting patients with chronic diseases.
Sernova Biotherapeutics has received FDA clearance for its Investigational New Drug application to evaluate the Cell Pouch bio-hybrid organ with auto-transplanted thyroid cells in patients undergoing thyroid surgery. This development marks a significant step forward in Sernova’s efforts to provide a long-term solution for hypothyroidism without the need for hormone replacement or immune suppression. The clearance allows Sernova to expand its clinical trials and strengthen its position in the regenerative medicine field.