Breakdown | ||||
Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|
Income Statement | Total Revenue | |||
0.00 | 0.00 | 0.00 | 0.00 | 0.00 | Gross Profit |
0.00 | 0.00 | 0.00 | 0.00 | 0.00 | EBIT |
-28.81M | -15.89M | -19.63M | -15.30M | -29.72M | EBITDA |
-28.79M | -15.88M | -11.76M | -15.24M | -29.67M | Net Income Common Stockholders |
-27.59M | -12.47M | -13.97M | -15.28M | -29.68M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | |||
16.02M | 22.43M | 33.36M | 16.39M | 10.09M | Total Assets |
16.26M | 22.78M | 33.53M | 16.80M | 10.97M | Total Debt |
136.00K | 203.00K | 0.00 | 71.00K | 94.00K | Net Debt |
-15.88M | -22.23M | -33.36M | -16.32M | -9.99M | Total Liabilities |
8.33M | 6.10M | 11.78M | 2.20M | 3.77M | Stockholders Equity |
7.93M | 16.68M | 21.75M | 14.60M | 7.20M |
Cash Flow | Free Cash Flow | |||
-24.72M | -10.85M | -11.71M | -15.14M | -10.77M | Operating Cash Flow |
-24.71M | -10.80M | -11.71M | -15.13M | -10.76M | Investing Cash Flow |
-8.00K | -50.00K | 8.00K | -586.00K | 69.00K | Financing Cash Flow |
18.30M | -80.00K | 28.68M | 22.03M | 6.86M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
51 Neutral | $5.20B | 3.26 | -40.34% | 2.93% | 17.68% | 1.94% | |
40 Underperform | $5.91M | ― | 422.38% | ― | -95.07% | 40.41% | |
39 Underperform | $6.49M | ― | -233.67% | ― | ― | ― | |
38 Underperform | $7.47M | ― | -331.94% | ― | 30.69% | 6.18% | |
34 Underperform | $6.11M | ― | ― | ― | -73095.97% | ||
33 Underperform | $15.92M | ― | -224.18% | ― | ― | -75.88% | |
24 Underperform | $7.26M | ― | -490.03% | ― | ― | 99.64% |
On April 22, 2025, MetaVia Inc. reported additional positive top-line results from the multiple ascending dose Part 2 of its Phase 1 clinical trial of DA-1726, a dual receptor agonist for obesity treatment. The trial demonstrated a dose-dependent response in body weight reduction and significant differences in BMI compared to placebo, without any drug-induced cardiovascular effects. The results suggest DA-1726’s potential as a best-in-class obesity treatment, with a robust safety profile and promising efficacy, particularly in higher doses. MetaVia plans to further explore the maximum tolerated dose and assess its potential in patients who have discontinued other treatments due to tolerability issues.
Spark’s Take on MTVA Stock
According to Spark, TipRanks’ AI Analyst, MTVA is a Underperform.
MetaVia’s stock score is heavily impacted by its poor financial performance, with persistent losses and no revenue. Despite positive trial results offering some promise, the stock remains high-risk due to negative valuation metrics and weak technical indicators.
To see Spark’s full report on MTVA stock, click here.
On April 15, 2025, MetaVia Inc. announced positive results from the multiple ascending dose Part 2 of its Phase 1 clinical trial for DA-1726, a dual oxyntomodulin analog agonist aimed at treating obesity. The trial demonstrated significant weight loss and safety effects, with a maximum weight reduction of 6.3% and mean reduction of 4.3% at a 32 mg dose. The study showed promising glucose control and waist reduction, with no serious adverse events reported. MetaVia plans to further explore the drug’s potential in a Phase 1 Part 3 study and additional cohorts to determine the maximum tolerated dose.
Spark’s Take on MTVA Stock
According to Spark, TipRanks’ AI Analyst, MTVA is a Underperform.
MetaVia’s overall stock score is significantly impacted by its poor financial performance, with persistent losses and a lack of revenue. The technical analysis suggests a weak market position with no upward momentum. Valuation metrics are unfavorable due to negative earnings, making it a high-risk investment. There is a pressing need for strategic operational improvements.
To see Spark’s full report on MTVA stock, click here.