| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 20.33M | 29.05M | 32.71M | 61.28M | 55.29M | 23.80M |
| Gross Profit | 19.60M | 28.14M | 31.11M | 48.15M | 46.32M | 21.74M |
| EBITDA | -996.95M | -1.10B | -802.89M | -1.18B | -910.77M | -720.58M |
| Net Income | -373.97M | -171.98M | 4.35B | -1.01B | -845.26M | -809.23M |
Balance Sheet | ||||||
| Total Assets | 5.06B | 5.44B | 7.22B | 2.39B | 2.59B | 2.69B |
| Cash, Cash Equivalents and Short-Term Investments | 4.39B | 4.89B | 6.54B | 1.68B | 2.06B | 2.13B |
| Total Debt | 98.85M | 100.17M | 499.75M | 481.40M | 283.89M | 244.98M |
| Total Liabilities | 257.14M | 249.74M | 773.95M | 782.02M | 523.70M | 527.69M |
| Stockholders Equity | 4.36B | 4.69B | 5.97B | 1.16B | 1.66B | 1.90B |
Cash Flow | ||||||
| Free Cash Flow | -784.38M | -844.05M | -766.65M | -856.08M | -695.16M | -557.94M |
| Operating Cash Flow | -769.86M | -839.45M | -765.27M | -843.39M | -677.73M | -552.14M |
| Investing Cash Flow | 562.97M | -1.77B | 5.20B | -44.27M | 303.30M | -31.70M |
| Financing Cash Flow | -575.28M | -1.22B | 419.36M | 499.46M | 306.79M | 456.26M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
76 Outperform | $8.75B | 97.47 | 16.47% | ― | 17.92% | -26.13% | |
73 Outperform | $7.28B | 13.17 | 124.50% | ― | 31.19% | 59.01% | |
68 Neutral | ― | ― | ― | ― | ― | 34.29% | |
64 Neutral | $10.27B | ― | -9.06% | ― | 4.14% | -179.96% | |
64 Neutral | $9.16B | 120.24 | 3.80% | 0.53% | 3.85% | -48.17% | |
58 Neutral | $14.21B | ― | -14.73% | ― | -83.82% | -109.22% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% |
On December 11, 2025, Roivant Sciences hosted its Investor Day, highlighting significant progress in its pipeline and outlining its growth strategy. The company announced plans for multiple product launches and filings over the next three years, including brepocitinib for dermatomyositis, with a commercial launch expected in early 2027. Roivant also reported positive updates on clinical trials, including accelerated timelines for brepocitinib in non-infectious uveitis and cutaneous sarcoidosis, as well as the IMVT-1402 trial for rheumatoid arthritis. Additionally, Roivant’s financing efforts have extended Immunovant’s cash runway to support the launch of IMVT-1402 in Graves’ disease, positioning the company for long-term shareholder value creation.
On September 17, 2025, Roivant Sciences announced positive results from the Phase 3 VALOR study of brepocitinib in dermatomyositis, marking the first successful 52-week placebo-controlled trial for this condition. The study demonstrated significant improvements in patients, with brepocitinib showing a clinically meaningful response compared to placebo on both primary and secondary endpoints, and a consistent safety profile. This breakthrough positions brepocitinib as a potential impactful treatment option for dermatomyositis, with an NDA filing planned for the first half of 2026.
On September 10, 2025, Roivant Sciences Ltd. held its Annual General Meeting of Shareholders, where all proposals on the agenda were approved. These included the re-election of Class I directors, the ratification of Ernst & Young LLP as the independent auditor, and a non-binding advisory vote on executive compensation. The meeting saw participation from holders of 628,673,675 common shares, reflecting strong shareholder engagement. The approval of these proposals is expected to reinforce Roivant’s governance structure and operational transparency, potentially enhancing its position in the biopharmaceutical industry.