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Theravance Biopharma (TBPH)
NASDAQ:TBPH
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Theravance Biopharma (TBPH) AI Stock Analysis

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TBPH

Theravance Biopharma

(NASDAQ:TBPH)

Rating:66Neutral
Price Target:
$15.00
▲(8.70% Upside)
Theravance Biopharma's overall stock score reflects strong technical momentum and positive corporate events, offset by high valuation concerns and ongoing profitability challenges. The company's strategic advancements and cash flow improvements are promising, but financial stability remains a key area for improvement.
Positive Factors
Analyst Recommendation
Analyst recommendation is a 'Buy' for Theravance Biopharma stock with a price target of 24.00.
Clinical Trial Results
The CYPRESS trial is significantly de-risked by preceding Phase 3 results where ampreloxetine showed positive trends without worsening of supine hypertension.
Market Need
A large majority of MSA patients with neurogenic orthostatic hypotension require pharmacologic treatment, indicating a strong market need.
Negative Factors
Current Treatment Limitations
Currently available treatment options are inadequate for up to 70% of patients, highlighting a gap in effective solutions.
Patient Management Challenges
About 50% of patients develop treatment limiting supine hypertension.

Theravance Biopharma (TBPH) vs. SPDR S&P 500 ETF (SPY)

Theravance Biopharma Business Overview & Revenue Model

Company DescriptionTheravance Biopharma, Inc., a biopharmaceutical company, discovers, develops, and commercializes respiratory medicines in the United States, Europe, and Asia. The company offers YUPELRI, a once-daily, nebulized long-acting muscarinic antagonist used for the treatment of chronic obstructive pulmonary disease (COPD). Its product portfolio also include Izencitinib, a gut-selective pan-janus kinase (JAK) inhibitor that is in Phase IIb/III clinical trials for the treatment of rheumatoid arthritis, myelofibrosis, and ulcerative colitis, as well as for a range of inflammatory intestinal diseases, including ulcerative colitis and Crohn's disease. In addition, the company's product portfolio comprise Ampreloxetine, an investigational norepinephrine reuptake inhibitor that has completed Phase III study for neurogenic orthostatic hypotension; Nezulcitinib, a lung-selective, nebulized JAK inhibitor, which is in Phase II clinical development for the potential treatment of hospitalized patients with acute lung injury caused by COVID-19; Inhaled ALK5i, a potential inhaled anti-fibrotic agent that is in Phase I for the treatment of idiopathic pulmonary fibrosis; and TD-5202, an investigational, orally administered, gut-selective, irreversible JAK3 inhibitor that is in Phase I clinical study for treatment of inflammatory intestinal diseases. Further, it offers TRELEGY for the treatment of COPD and asthma; Velusetrag, an oral and investigational medicine for gastrointestinal motility disorders; and Selective 5-HT4 Agonist for treatment of gastrointestinal motility disorders. It has a licensing and collaboration agreements with Pfizer Inc., Viatris Inc., Janssen Biotech, Inc., Alfasigma S.p.A, and Takeda Pharmaceutical Company Limited. Theravance Biopharma, Inc. was incorporated in 2013 and is based in George Town, the Cayman Islands.
How the Company Makes MoneyTheravance Biopharma generates revenue through multiple streams, primarily from the sale of its pharmaceutical products, particularly Vibativ. Additionally, the company earns revenue through collaboration agreements and licensing partnerships with other pharmaceutical companies, which may include upfront payments, milestone payments, and royalties on product sales. The company may also receive funding through grants and research contracts aimed at supporting its drug development initiatives. Significant partnerships with larger pharmaceutical firms can enhance its revenue potential by providing financial resources and broader market access for its products.

Theravance Biopharma Earnings Call Summary

Earnings Call Date:Aug 12, 2025
(Q2-2025)
|
% Change Since: |
Next Earnings Date:Nov 05, 2025
Earnings Call Sentiment Positive
The earnings call showcased a strong financial performance with significant growth in YUPELRI sales and strategic financial transactions that bolster Theravance's balance sheet. The advancement of the ampreloxetine trial and strong TRELEGY performance add to the positive outlook. However, uncertainties around YUPELRI's launch in China and tax liabilities from recent transactions were noted as slight concerns.
Q2-2025 Updates
Positive Updates
Strong YUPELRI Performance
Net sales for YUPELRI reached approximately $66 million, a 22% increase year-over-year, marking the highest Q2 result since launch. This growth was driven by demand growth, net price improvement, and a onetime favorable adjustment to net pricing.
Strategic Financial Transactions
Completed a $225 million sale of remaining royalty interest in TRELEGY to GSK, significantly strengthening the balance sheet. The transaction increases the likelihood of receiving $150 million in milestones from Royalty Pharma in the next 18 months.
Advancement in Ampreloxetine Development
The Phase III CYPRESS trial for ampreloxetine is progressing well, with enrollment expected to complete soon. This program is seen as having potential to bring great value to patients with MSA and shareholders.
Financial Strength and Cash Position
Ended the quarter with approximately $340 million in cash and no debt. Operations remain near cash neutral, highlighting strong cash management.
TRELEGY's Strong Performance
GSK reported an all-time high of $1.1 billion in sales for TRELEGY, putting Theravance on track to exceed a $3.4 billion annual sales threshold in 2025, triggering a $50 million milestone payment.
Negative Updates
Limited Information on YUPELRI Launch in China
While YUPELRI received approval in China, specifics on the launch plan and timing remain vague as Viatris finalizes the commercialization strategy.
Tax Liabilities from TRELEGY Sale
Expected to pay approximately $27 million in taxes related to the TRELEGY royalty sale in the second half of the year, which could impact cash flow.
Company Guidance
During the Theravance Biopharma Second Quarter 2025 Conference Call, CEO Rick Winningham highlighted the company's strong financial performance and strategic advancements. Key metrics included YUPELRI's net sales reaching approximately $66 million, a 22% year-over-year increase, driven by demand growth and favorable pricing, notably achieving a 31% increase in hospital channel volume. The company also completed a $225 million sale of its remaining royalty interest in TRELEGY to GSK, strengthening the balance sheet with expectations of receiving $150 million in milestones from Royalty Pharma in the next 18 months. The CYPRESS Phase III trial for ampreloxetine in patients with multiple system atrophy (MSA) remained on track for completion, with a focus on delivering top-line data in six months. Theravance ended the quarter with $340 million in cash and no debt, maintaining operations near cash neutral, and reaffirmed its 2025 financial guidance, anticipating improvements in non-GAAP losses and cash burn compared to 2024.

Theravance Biopharma Financial Statement Overview

Summary
Theravance Biopharma shows positive revenue and cash flow growth, indicating potential recovery. However, persistent profitability challenges and historical negative cash flows suggest underlying financial instability. The company needs to improve operational efficiency and profitability to enhance its financial health.
Income Statement
45
Neutral
Theravance Biopharma shows a positive revenue growth rate of 18.29% TTM, indicating a recovery trend. However, the company struggles with profitability, as evidenced by negative EBIT and net profit margins. The gross profit margin remains strong at 100%, but the negative net profit margin suggests challenges in managing operating expenses.
Balance Sheet
50
Neutral
The company's debt-to-equity ratio is relatively low at 0.29 TTM, indicating manageable leverage. However, the negative return on equity highlights ongoing profitability issues. The equity ratio is not provided, but the overall balance sheet suggests moderate financial stability with potential risks due to negative ROE.
Cash Flow
60
Neutral
Theravance Biopharma shows a significant improvement in free cash flow growth at 658.17% TTM, reflecting enhanced cash generation capabilities. The operating cash flow to net income ratio is positive, indicating efficient cash flow management. However, historical negative cash flows pose a risk to sustainability.
BreakdownTTMDec 2024Dec 2023Dec 2022Dec 2021Dec 2020
Income Statement
Total Revenue77.20M64.38M57.42M51.35M55.31M71.86M
Gross Profit77.20M64.38M57.42M44.76M48.02M-189.10M
EBITDA46.09M-38.45M-42.66M-79.86M-249.39M-294.00M
Net Income13.03M-56.42M-55.19M-92.82M-199.43M-278.02M
Balance Sheet
Total Assets426.04M354.16M382.00M607.40M374.82M469.06M
Cash, Cash Equivalents and Short-Term Investments338.80M88.35M102.43M327.48M173.47M292.94M
Total Debt46.46M49.82M49.16M74.12M652.08M647.06M
Total Liabilities201.19M178.62M169.00M165.60M713.39M772.81M
Stockholders Equity224.85M175.54M213.00M441.80M-338.57M-303.75M
Cash Flow
Free Cash Flow244.78M-11.87M-29.48M-187.56M-211.26M-257.02M
Operating Cash Flow245.01M-11.54M-27.00M-186.99M-207.86M-250.40M
Investing Cash Flow-7.34M12.28M-32.70M1.15B124.49M10.72M
Financing Cash Flow-2.09M-2.50M-198.93M-758.81M91.86M263.08M

Theravance Biopharma Technical Analysis

Technical Analysis Sentiment
Positive
Last Price13.80
Price Trends
50DMA
11.66
Positive
100DMA
10.62
Positive
200DMA
10.01
Positive
Market Momentum
MACD
0.72
Negative
RSI
76.83
Negative
STOCH
73.78
Neutral
Evaluating momentum and price trends is crucial in stock analysis to make informed investment decisions. For TBPH, the sentiment is Positive. The current price of 13.8 is above the 20-day moving average (MA) of 12.48, above the 50-day MA of 11.66, and above the 200-day MA of 10.01, indicating a bullish trend. The MACD of 0.72 indicates Negative momentum. The RSI at 76.83 is Negative, neither overbought nor oversold. The STOCH value of 73.78 is Neutral, not indicating any strong overbought or oversold conditions. Overall, these indicators collectively point to a Positive sentiment for TBPH.

Theravance Biopharma Risk Analysis

Theravance Biopharma disclosed 46 risk factors in its most recent earnings report. Theravance Biopharma reported the most risks in the "Finance & Corporate" category.
Finance & Corporate - Financial and accounting risks. Risks related to the execution of corporate activity and strategy
Latest Risks Added 0 New Risks

Theravance Biopharma Peers Comparison

Overall Rating
UnderperformOutperform
Sector (51)
Financial Indicators
Name
Overall Rating
Market Cap
P/E Ratio
ROE
Dividend Yield
Revenue Growth
EPS Growth
66
Neutral
$694.99M59.006.23%24.49%
66
Neutral
$605.58M49.543.33%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%
* Healthcare Sector Average
Performance Comparison
Ticker
Company Name
Price
Change
% Change
TBPH
Theravance Biopharma
13.80
5.59
68.09%
SAGE
SAGE Therapeutics
8.68
0.59
7.29%
CAPR
Capricor Therapeutics
6.25
1.55
32.98%
MNMD
Mind Medicine
9.85
3.84
63.89%
MGTX
Meiragtx Holdings
7.44
3.26
77.99%
KROS
Keros Therapeutics
15.52
-29.79
-65.75%

Theravance Biopharma Corporate Events

Product-Related AnnouncementsBusiness Operations and Strategy
Theravance Completes Enrollment in Phase 3 CYPRESS Study
Positive
Aug 25, 2025

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.

Legal Proceedings
Theravance Biopharma Settles Patent Dispute with Cipla
Neutral
Aug 20, 2025

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.

Product-Related AnnouncementsBusiness Operations and Strategy
Theravance Biopharma Gains Milestone Payment from Viatris
Positive
Jun 26, 2025

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.

Legal Proceedings
Theravance Biopharma Settles Patent Litigation with Eugia
Neutral
Jun 6, 2025

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.

M&A TransactionsBusiness Operations and Strategy
Theravance Biopharma Sells Trelegy Royalty Interest to GSK
Neutral
Jun 2, 2025

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.

Glossary
BuyA stock rated as a "Buy" is expected to perform better than the overall market or a specific benchmark over the near-to-medium term. This rating suggests the stock is likely to deliver higher returns compared to other stocks in the same sector or market index. Note: This is not investment advice; please consult a financial advisor before making investment decisions.
HoldA stock rated as a "Hold" is expected to perform in line with the overall market or a specific benchmark. This rating indicates that the stock is neither particularly compelling nor unfavorable for investment. Note: This is not investment advice; please consult a financial advisor before making investment decisions.
SellA stock rated as a "Sell" is expected to perform worse than the overall market or a specific benchmark over the near-to-medium term. This rating suggests the stock may deliver lower returns compared to other stocks in the same sector or market index. Note: This is not investment advice; please consult a financial advisor before making investment decisions.

Disclaimer

This AI Analyst Stock Report is automatically generated by our AI systems using advanced algorithms and publicly available financial, technical, and market data. While the information provided aims to be accurate and insightful, it is intended for informational purposes only and should not be considered financial advice. Any content created by an AI (Artificial Intelligence) system may contain inaccuracies and/or contain errors. Investing in stocks carries inherent risks, and past performance is not indicative of future results. This report does not account for your personal financial circumstances, objectives, or risk tolerance. Always conduct your own research or consult with a qualified financial advisor before making investment decisions. The analysis and recommendations provided are based on historical and current data and may not fully reflect future market conditions or unexpected developments. Neither the creators of this report nor its affiliated entities guarantee the accuracy, completeness, or reliability of the information presented. Use this report at your own discretion and risk.Date of analysis: Aug 25, 2025