Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|---|---|
Income Statement | ||||||
Total Revenue | 77.20M | 64.38M | 57.42M | 51.35M | 55.31M | 71.86M |
Gross Profit | 77.20M | 64.38M | 57.42M | 44.76M | 48.02M | -189.10M |
EBITDA | 46.09M | -38.45M | -42.66M | -79.86M | -249.39M | -294.00M |
Net Income | 13.03M | -56.42M | -55.19M | -92.82M | -199.43M | -278.02M |
Balance Sheet | ||||||
Total Assets | 426.04M | 354.16M | 382.00M | 607.40M | 374.82M | 469.06M |
Cash, Cash Equivalents and Short-Term Investments | 338.80M | 88.35M | 102.43M | 327.48M | 173.47M | 292.94M |
Total Debt | 46.46M | 49.82M | 49.16M | 74.12M | 652.08M | 647.06M |
Total Liabilities | 201.19M | 178.62M | 169.00M | 165.60M | 713.39M | 772.81M |
Stockholders Equity | 224.85M | 175.54M | 213.00M | 441.80M | -338.57M | -303.75M |
Cash Flow | ||||||
Free Cash Flow | 244.78M | -11.87M | -29.48M | -187.56M | -211.26M | -257.02M |
Operating Cash Flow | 245.01M | -11.54M | -27.00M | -186.99M | -207.86M | -250.40M |
Investing Cash Flow | -7.34M | 12.28M | -32.70M | 1.15B | 124.49M | 10.72M |
Financing Cash Flow | -2.09M | -2.50M | -198.93M | -758.81M | 91.86M | 263.08M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
66 Neutral | $694.99M | 59.00 | 6.23% | ― | 24.49% | ― | |
66 Neutral | $605.58M | 49.54 | 3.33% | ― | 85820.30% | ― | |
54 Neutral | ― | ― | -27.59% | 34.00% | |||
51 Neutral | $7.83B | -0.18 | -40.10% | 2.29% | 21.46% | -2.03% | |
43 Neutral | $295.79M | ― | -120.15% | ― | -50.68% | -76.38% | |
41 Neutral | $603.36M | ― | -379.53% | ― | 366.84% | -35.87% | |
40 Neutral | $760.12M | ― | -59.11% | ― | ― | 39.66% |
On August 25, 2025, Theravance Biopharma announced the completion of enrollment in the open-label portion of its pivotal Phase 3 CYPRESS study for ampreloxetine, targeting symptomatic neurogenic orthostatic hypotension (nOH) due to multiple system atrophy (MSA). This condition affects approximately 80% of MSA patients, leading to severe symptoms like dizziness and fainting. The study aims to address the unmet need for effective nOH treatments, with topline results expected in Q1 2026. If successful, ampreloxetine could become the first therapy to provide durable benefits for the estimated 40,000 U.S. patients with MSA-related nOH, potentially transforming treatment options in this underserved market.
On August 15, 2025, Theravance Biopharma and Mylan entered into a Settlement Agreement with Cipla to resolve ongoing patent litigation over YUPELRI® inhalation solution. The agreement allows Cipla to manufacture and market a generic version of YUPELRI® in the U.S. starting April 23, 2039, pending review by U.S. authorities, while litigation continues against Mankind Pharma Ltd.
On June 26, 2025, Theravance Biopharma announced that Viatris secured regulatory approval from China’s NMPA for YUPELRI® (revefenacin) inhalation solution, marking it as the first once-daily nebulized LAMA for COPD maintenance treatment in China. This approval triggers a $7.5 million milestone payment from Viatris to Theravance, expected in Q3 2025, and positions Theravance for further sales-based milestones and royalties, enhancing its financial standing without incurring commercial costs in China.
On June 5, 2025, Theravance Biopharma and Mylan entered into a Settlement Agreement with Eugia Pharma to resolve ongoing patent litigation concerning the YUPELRI® inhalation solution. The agreement allows Eugia to manufacture and market a generic version of YUPELRI® in the U.S. starting April 23, 2039, pending review by the U.S. Department of Justice and the Federal Trade Commission, while litigation continues against other ANDA filers.
On May 30, 2025, Theravance Biopharma entered into an agreement with GlaxoSmithKline (GSK) to sell its remaining royalty interest in Trelegy Ellipta for $225 million. This transaction, part of the company’s strategic efforts to maximize shareholder value, follows a previous sale of Trelegy royalty interests in 2022 for $1.1 billion. The deal underscores Theravance Biopharma’s strategy to monetize its assets while retaining rights to potential milestone payments from Royalty Pharma.