Breakdown | |||||
TTM | Mar 2024 | Mar 2023 | Mar 2022 | Mar 2021 | Mar 2020 |
---|---|---|---|---|---|
Income Statement | Total Revenue | ||||
4.04M | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | Gross Profit |
2.65M | -2.65M | -2.45M | -4.58M | -4.14M | -1.81M | EBIT |
-241.06M | -234.77M | -177.08M | -118.31M | -79.95M | -56.20M | EBITDA |
-217.67M | -230.20M | -170.30M | -114.41M | -76.48M | -52.60M | Net Income Common Stockholders |
-228.24M | -215.79M | -174.28M | -118.04M | -80.87M | -52.63M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | ||||
420.67M | 420.67M | 583.39M | 395.65M | 476.30M | 168.56M | Total Assets |
487.72M | 487.72M | 646.59M | 461.19M | 543.10M | 234.10M | Total Debt |
75.87M | 75.87M | 60.76M | 32.84M | 33.28M | 41.79M | Net Debt |
1.41M | 1.41M | -85.83M | -73.11M | -149.24M | -17.71M | Total Liabilities |
113.21M | 113.21M | 91.30M | 49.96M | 44.37M | 50.38M | Stockholders Equity |
374.51M | 374.51M | 555.29M | 411.23M | 498.73M | 183.72M |
Cash Flow | Free Cash Flow | ||||
-191.98M | -191.13M | -130.32M | -84.52M | -63.78M | -67.09M | Operating Cash Flow |
-184.69M | -185.47M | -128.05M | -82.18M | -61.39M | -60.55M | Investing Cash Flow |
7.11M | 97.20M | -142.50M | -1.81M | -188.78M | -5.23M | Financing Cash Flow |
252.40M | 16.28M | 311.30M | 6.60M | 372.46M | 100.17M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
56 Neutral | $26.29B | ― | -2.44% | ― | -52.11% | -118.03% | |
53 Neutral | $976.55M | ― | -47.32% | ― | ― | 4.28% | |
49 Neutral | $7.05B | 0.34 | -55.09% | 2.46% | 25.27% | -3.43% | |
48 Neutral | $11.72B | ― | -32.67% | ― | -52.75% | 25.00% | |
44 Neutral | $123.85M | ― | -56.17% | ― | 145.37% | 57.01% | |
42 Neutral | $518.00M | ― | -14.59% | ― | ― | ― |
Replimune Group, Inc. has made significant strides in cancer treatment with its submission of a biologics license application to the FDA for its lead product, RP1, in combination with nivolumab, targeting advanced melanoma. The FDA has granted Breakthrough Therapy designation to this innovative therapy, which could expedite its availability for patients with limited options. This development marks a promising advancement for Replimune, as their novel oncolytic immunotherapy shows potential for substantial improvement over existing treatments.