| 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 |
|---|---|---|---|---|---|---|---|
| ― | $684.57M | ― | -43.63% | ― | ― | -13.05% | |
| ― | $766.50M | 65.07 | 6.23% | ― | 24.49% | ― | |
| ― | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
| ― | $748.78M | ― | -24.75% | ― | 2190.50% | 52.85% | |
| ― | $801.84M | ― | -55.41% | ― | -22.52% | -37.00% | |
| ― | $722.84M | ― | -35.02% | ― | ― | 20.37% | |
| ― | $988.89M | ― | ― | ― | ― | ― |
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.
The most recent analyst rating on (TBPH) stock is a Hold with a $14.50 price target. To see the full list of analyst forecasts on Theravance Biopharma stock, see the TBPH Stock Forecast page.
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.
The most recent analyst rating on (TBPH) stock is a Buy with a $26.00 price target. To see the full list of analyst forecasts on Theravance Biopharma stock, see the TBPH Stock Forecast page.
Theravance Biopharma’s recent earnings call painted a picture of strong financial performance and strategic maneuvers, particularly with its key products YUPELRI and TRELEGY. The company showcased its momentum and financial strength, although some uncertainties linger regarding the YUPELRI launch in China and pending tax obligations.
Theravance Biopharma, Inc. is a biopharmaceutical company focused on developing and commercializing respiratory and neurological therapies, with a notable emphasis on its FDA-approved YUPELRI® for COPD and investigational drug ampreloxetine for neurogenic orthostatic hypotension in MSA patients.