🏢 官网IRUTHRCodex · 实盘不做把握 6/10
北京时间·🕒 发布 19:30:00待核·⟳ 抓取 18:30:30·⚡ 决策 08-05 22:09:53 +3h39m·82.9 天前
United Therapeutics二季度收入同比下降但EPS增长,并称已提交两项罕见肺病NDA
United Therapeutics(UTHR.US)二季度收入7.833亿美元同比下降2%,Tyvaso收入同比下降4%,但净利润同比增长8%、摊薄EPS同比增长13%,财报方向并不单边。
📄 原文UTHR↗ 原文
United Therapeutics Corporation Reports Second Quarter 2026 Financial Results
“We just submitted what we believe are two of the most important NDAs in rare pulmonary disease history: ralinepag tabl…
不做 United Therapeutics(UTHR.US)
财报和管线申报方向混合:收入和Tyvaso下滑削弱追多,EPS增长和长期NDA期权又不构成强空;申报节点此前已有预期,当前不做。
不做 Liquidia(LQDA.US)
竞争受益只是UTHR财报中的间接读-through,未披露LQDA新增销售或指引;股价已接近52周高位且当日已涨,不追。
展开详情(成交明细 / 研究档案 / 原文全文 / 决策记录链)
研究档案
消息传播链
- 公司官方发布二季度财报,并披露ralinepag片剂PAH与Nebulized Tyvaso IPF两项NDA已提交。
- 2026-08-05 10:06 ET市场反应stock_quote/futu非一手UTHR盘中报价520.57美元,较前收518.68美元涨0.36%;日内曾开在505美元、低见490.8美元后回升,市场未给出单边利好确认。市场反应:UTHR.US +0.36%;LQDA.US +3.27%。
关键理由
- United Therapeutics(UTHR.US)二季度收入7.833亿美元同比下降2%,Tyvaso收入同比下降4%,但净利润同比增长8%、摊薄EPS同比增长13%,财报方向并不单边。
- 公司称ralinepag片剂PAH和Nebulized Tyvaso IPF两项NDA已提交、潜在为数十亿美元级催化,但内部KB显示Tyvaso IPF和ralinepag在2026年内临近申报/数据已被多篇研报和投资文章提前讨论,不是完全新的预期差。
- 现有Tyvaso季度销售4.526亿美元、公司总季度收入7.833亿美元;IPF/PAH扩适应症若获批长期空间可能大,但本次只是申报节点,新增可触达收入要等2027年潜在批准与渗透,短线无法直接量化成收入或利润增量。
主要风险
- 若电话会给出超预期审批时间表、标签范围或销售指引,上述“不做”可能低估管线期权重定价。
- Liquidia(LQDA.US)作为竞争对手已有强势重估,UTHR财报中的竞争压力读-through不足以在当前价位追多LQDA。
反向证据
- 做多前查反向 · 来源 kb_search · 日期 2026-05-13 · 影响 weakens
研报已提前讨论ralinepag、Tyvaso IPF/PPF机会,申报本身预期差不足。
检索:United Therapeutics Q2 2026 Tyvaso IPF ralinepag NDA sales consensus 原文 ↗ - 做多前查反向 · 来源 kb_search · 日期 2026-02-25 · 影响 weakens
KB显示Tyvaso此前多个季度低于一致预期且受Liquidia Yutrepia竞争影响,削弱对UTHR财报追多的确定性。
检索:United Therapeutics Tyvaso IPF ralinepag revenue opportunity risk litigation generic competition 2026 原文 ↗ - 做空前查反向 · 来源 stock_quote · 日期 2026-08-05 · 影响 weakens
UTHR开盘下跌后回升至小幅上涨,且净利润/EPS同比增长,不满足强空催化。
检索:UTHR.US stock_quote full current price reaction - 做多前查反向 · 来源 kb_search · 日期 2026-07-22 · 影响 weakens
LQDA受益逻辑已被市场交易,KB显示一年涨幅极大且当前股价接近52周高位,本条只属间接确认。
检索:Liquidia Yutrepia launch competitive impact Tyvaso United Therapeutics 2026 sales share 原文 ↗
工具调用 · 历史记录,结果未知(3 种)
- search_processed_events · 结果未知
- stock_quote · 结果未知
- kb_search · 结果未知
原文全文
展开原文 · 15,443 字
United Therapeutics Corporation Reports Second Quarter 2026 Financial Results
“We just submitted what we believe are two of the most important NDAs in rare pulmonary disease history: ralinepag tablets in PAH and Nebulized Tyvaso in IPF,” said Martine Rothblatt, Ph.D., Chairperson and Chief Executive Officer of United Therapeutics. “We believe that these submissions, accompanied by our planned filings later this year – an IND application for ralinepag DPI and an NDA for treprostinil SMI – may herald an opportunity for a quantum increase in our growth by the end of the decade. By next year, we expect potential approvals for Nebulized Tyvaso in IPF and ralinepag tablets in PAH, two potentially transformative, multi-billion-dollar catalysts that could significantly enhance our growth profile. We expect Tyvaso DPI will then follow Nebulized Tyvaso’s wake into IPF and then PPF. Moreover, our organ manufacturing pipeline continues to advance rapidly with clinical trials ongoing or being planned for liver, kidney, heart, and lung products, and the launch later this year of two xeno-organ production facilities in
“Tyvaso DPI exited the second quarter at record levels of starts, referrals, commercial patients, and total patients, reflecting strong underlying demand,” said Michael Benkowitz, President and Chief Operating Officer of United Therapeutics. “Supported by our competitively differentiated device, deep clinical experience, and significant remaining opportunity in PH-ILD, we are confident in our ability to extend our leadership position in the inhaled prostacyclin class.”
Second Quarter 2026 Financial Results
Key financial highlights include (dollars in millions, except per share data):
| Three Months Ended June 30, |
| Dollar
|
| Percentage
| |||||||
|
| 2026 |
|
| 2025 |
|
| |||||
|
|
|
|
|
|
|
| |||||
Total revenues | $ | 783.3 |
| $ | 798.6 |
| $ | (15.3 | ) |
| (2 | )% |
Net income | $ | 333.0 |
| $ | 309.5 |
| $ | 23.5 |
|
| 8 | % |
Net income, per basic share | $ | 7.82 |
| $ | 6.86 |
| $ | 0.96 |
|
| 14 | % |
Net income, per diluted share | $ | 7.27 |
| $ | 6.41 |
| $ | 0.86 |
|
| 13 | % |
Revenues
The table below presents the components of total revenues (dollars in millions):
| Three Months Ended June 30, |
| Dollar
|
| Percentage
| |||||||
|
| 2026 |
|
| 2025 |
|
| |||||
Net product sales: |
|
|
|
|
|
|
| |||||
Tyvaso DPI® | $ | 326.6 |
| $ | 315.2 |
| $ | 11.4 |
|
| 4 | % |
Nebulized Tyvaso® |
| 126.0 |
|
| 154.4 |
|
| (28.4 | ) |
| (18 | )% |
Total Tyvaso |
| 452.6 |
|
| 469.6 |
|
| (17.0 | ) |
| (4 | )% |
Remodulin®(1) |
| 126.3 |
|
| 134.7 |
|
| (8.4 | ) |
| (6 | )% |
Orenitram® |
| 125.7 |
|
| 123.9 |
|
| 1.8 |
|
| 1 | % |
Unituxin® |
| 65.2 |
|
| 58.4 |
|
| 6.8 |
|
| 12 | % |
Adcirca® |
| 6.7 |
|
| 6.5 |
|
| 0.2 |
|
| 3 | % |
Other |
| 6.8 |
|
| 5.5 |
|
| 1.3 |
|
| 24 | % |
Total revenues | $ | 783.3 |
| $ | 798.6 |
| $ | (15.3 | ) |
| (2 | )% |
(1) | Net product sales include sales of infusion devices, including the Remunity® and RemunityPRO® Pumps. |
Total Tyvaso revenues decreased by four percent to
The table below presents the breakdown of total revenues between
| Three Months Ended June 30, | ||||||||||||||||
| 2026 |
| 2025 | ||||||||||||||
| ROW | Total |
| ROW | Total | ||||||||||||
Net product sales: |
|
|
|
|
|
|
| ||||||||||
Tyvaso DPI | $ | 326.6 | $ | — | $ | 326.6 |
| $ | 314.8 | $ | 0.4 | $ | 315.2 | ||||
Nebulized Tyvaso |
| 109.7 |
| 16.3 |
| 126.0 |
|
| 140.5 |
| 13.9 |
| 154.4 | ||||
Total Tyvaso |
| 436.3 |
| 16.3 |
| 452.6 |
|
| 455.3 |
| 14.3 |
| 469.6 | ||||
Remodulin(1) |
| 99.4 |
| 26.9 |
| 126.3 |
|
| 113.7 |
| 21.0 |
| 134.7 | ||||
Orenitram |
| 125.7 |
| — |
| 125.7 |
|
| 123.9 |
| — |
| 123.9 | ||||
Unituxin |
| 59.0 |
| 6.2 |
| 65.2 |
|
| 55.4 |
| 3.0 |
| 58.4 | ||||
Adcirca |
| 6.7 |
| — |
| 6.7 |
|
| 6.5 |
| — |
| 6.5 | ||||
Other |
| 6.5 |
| 0.3 |
| 6.8 |
|
| 5.0 |
| 0.5 |
| 5.5 | ||||
Total revenues | $ | 733.6 | $ | 49.7 | $ | 783.3 |
| $ | 759.8 | $ | 38.8 | $ | 798.6 | ||||
(1) | Net product sales include sales of infusion devices, including the Remunity and RemunityPRO Pumps. |
Expenses
Cost of sales. The table below summarizes cost of sales by major category (dollars in millions):
| Three Months Ended June 30, |
| Dollar
|
| Percentage
| ||||||
|
| 2026 |
|
| 2025 |
|
| ||||
Category: |
|
|
|
|
|
|
| ||||
Cost of sales | $ | 98.5 |
| $ | 86.6 |
| $ | 11.9 |
| 14 | % |
Share-based compensation expense(1) |
| 1.0 |
|
| 1.0 |
|
| — |
| — | % |
Total cost of sales | $ | 99.5 |
| $ | 87.6 |
| $ | 11.9 |
| 14 | % |
(1) | See Share-based compensationexpense below for discussion. |
Cost of sales, excluding share-based compensation. The increase in cost of sales for the three months ended June 30, 2026, as compared to the same period in 2025, was primarily due to an increase in inventory reserve expense. Of this increased amount,
Research and development expense. The table below summarizes the nature of research and development expense by major expense category (dollars in millions):
| Three Months Ended June 30, |
| Dollar
|
| Percentage
| |||||||
|
| 2026 |
|
| 2025 |
|
| |||||
Category: |
|
|
|
|
|
|
| |||||
External research and development(1) | $ | 71.2 |
| $ | 62.4 |
| $ | 8.8 |
|
| 14 | % |
Internal research and development(2) |
| 54.0 |
|
| 55.9 |
|
| (1.9 | ) |
| (3 | )% |
Share-based compensation expense(3) |
| 10.9 |
|
| 8.1 |
|
| 2.8 |
|
| 35 | % |
Other(4) |
| 10.2 |
|
| 7.6 |
|
| 2.6 |
|
| 34 | % |
Total research and development expense | $ | 146.3 |
| $ | 134.0 |
| $ | 12.3 |
|
| 9 | % |
(1) | External research and development primarily includes fees paid to third parties (such as clinical trial sites, contract research organizations, and contract laboratories) for preclinical and clinical studies and payments to third-party contract manufacturers before regulatory approval of the relevant product. |
(2) | Internal research and development primarily includes salary-related expenses for research and development functions, internal costs to manufacture product candidates before regulatory approval, and internal facilities-related expenses, including depreciation, related to research and development activities. |
(3) | See Share-based compensation expense below for discussion. |
(4) | Other primarily includes upfront fees and milestone payments to third parties under license agreements related to development-stage products and adjustments to the fair value of our contingent consideration obligations. |
Research and development, excluding share-based compensation. The increase in research and development expense for the three months ended June 30, 2026, as compared to the same period in 2025, was primarily due to: (1) an increase in expenditures related to cardiopulmonary treatment projects; and (2) an increase in the fair value of our contingent consideration obligations for manufactured organ and organ alternative projects obtained through acquisition.
Selling, general, and administrative expense. The table below summarizes selling, general, and administrative expense by major category (dollars in millions):
| Three Months Ended June 30, |
| Dollar
|
| Percentage
| |||||||
|
| 2026 |
|
| 2025 |
|
| |||||
Category: |
|
|
|
|
|
|
| |||||
General and administrative(1) | $ | 137.9 |
| $ | 131.1 |
| $ | 6.8 |
|
| 5 | % |
Impairment of property, plant, and equipment (PP&E) |
| — |
|
| 21.7 |
|
| (21.7 | ) |
| (100 | )% |
Sales and marketing |
| 37.3 |
|
| 31.0 |
|
| 6.3 |
|
| 20 | % |
Share-based compensation expense(2) |
| 31.5 |
|
| 28.7 |
|
| 2.8 |
|
| 10 | % |
Total selling, general, and administrative expense | $ | 206.7 |
| $ | 212.5 |
| $ | (5.8 | ) |
| (3 | )% |
(1) | Excluding impairment of PP&E. See Impairment of PP&E section below. |
(2) | See Share-based compensation expense below for discussion. |
General and administrative, excluding impairment of PP&E and share-based compensation. The increase in general and administrative expense for the three months ended June 30, 2026, as compared to the same period in 2025, was primarily due to: (1) an increase in personnel expense due to growth in headcount; and (2) an increase in consulting expenses, partially offset by a decrease in legal expenses related to litigation matters.
Impairment of PP&E. The decrease in impairment of PP&E during the three months ended June 30, 2026, as compared to the same period in 2025, was primarily due to the impairment charge to write down the carrying value of certain PP&E in 2025, which did not recur in 2026.
Sales and marketing, excluding share-based compensation. The increase in sales and marketing expense for the three months ended June 30, 2026, as compared to the same period in 2025, was primarily due to an increase in personnel expense due to growth in headcount.
Share-based compensation expense. The table below summarizes share-based compensation expense by major category (dollars in millions):
| Three Months Ended June 30, |
| Dollar
|
| Percentage
| ||||||
|
| 2026 |
|
| 2025 |
|
| ||||
Category: |
|
|
|
|
|
|
| ||||
Stock options | $ | 12.8 |
| $ | 11.1 |
| $ | 1.7 |
| 15 | % |
Restricted stock units |
| 29.7 |
|
| 26.0 |
|
| 3.7 |
| 14 | % |
Employee stock purchase plan |
| 0.9 |
|
| 0.7 |
|
| 0.2 |
| 29 | % |
Total share-based compensation expense | $ | 43.4 |
| $ | 37.8 |
| $ | 5.6 |
| 15 | % |
Interest income. Interest income was
Other income (expense), net. Other income (expense), net for the three months ended June 30, 2026 and 2025 was
Income tax expense. Income tax expense for the three months ended June 30, 2026 and 2025 was
Share repurchase. In March 2026, our Board of Directors approved a share repurchase program authorizing up to
Webcast
We will host a webcast to discuss our second quarter 2026 financial results on Wednesday, August 5, 2026, at 9:00 a.m. Eastern Time. The webcast can be accessed live via our website at https://ir.unither.com/events-and-presentations. An investor presentation is available now, and after the webcast a replay of the webcast will also be available, at the same location on our website.
About United Therapeutics
Founded by CEO Martine Rothblatt to discover a cure for her daughter's life-threatening rare disease, pulmonary arterial hypertension, United Therapeutics transforms the treatment of rare diseases and pioneers alternatives to expand the supply of transplantable organs. From our innovative therapies to our groundbreaking manufactured organs, we are bold and unconventional. We move quickly from scientific theory to practical technologies that can save lives. As a public benefit corporation, even our legal structure reflects our commitments. We serve patients, act with integrity, create long-term shareholder value, and operate with sustainable practices that protect the future we are working to build.
Forward-Looking Statements
Statements included in this press release that are not historical in nature are “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements include statements related to: our research and development and regulatory plans, including the potential outcome of our NDA and sNDA seeking approval for ralinepag tablets for PAH and Nebulized Tyvaso for IPF, respectively, our plans to submit by the end of this year an IND for ralinepag DPI and an NDA for treprostinil SMI, our plans to develop Tyvaso DPI for IPF and PPF; the potential for us to achieve a quantum increase in our growth by the end of the decade; our expectation that ralinepag tablets and Nebulized Tyvaso for IPF represent multi-billion-dollar catalysts that could significantly enhance our growth profile; our organ manufacturing pipeline, including our planned clinical trials and our plan to launch new xeno-organ facilities later this year; our expectation that our competitively differentiated device, deep clinical experience, and significant remaining opportunity in PH-ILD will enable us to extend our leadership position in the inhaled prostacyclin class; and our goals of expanding the supply of transplantable organs, developing practical technologies that can save lives, creating long-term shareholder value, and operating with sustainable practices. These forward-looking statements are subject to certain risks and uncertainties, such as those described in our periodic reports filed with the Securities and Exchange Commission, that could cause actual results to differ materially from anticipated results. Consequently, such forward-looking statements are qualified by the cautionary statements, cautionary language and risk factors set forth in our periodic reports and documents filed with the Securities and Exchange Commission, including our most recent Annual Report on Form 10-K, Quarterly Reports on Form 10-Q, and Current Reports on Form 8-K. We claim the protection of the safe harbor contained in the Private Securities Litigation Reform Act of 1995 for forward-looking statements. We are providing this information as of August 5, 2026, and assume no obligation to update or revise the information contained in this press release whether as a result of new information, future events, or any other reason.
ORENITRAM, REMODULIN, REMUNITY, REMUNITYPRO, TYVASO, TYVASO DPI, and UNITUXIN are registered trademarks of United Therapeutics Corporation.
ADCIRCA is a registered trademark of Eli Lilly and Company.
Abbreviations:
1. NDA = new drug application. 2. PAH = pulmonary arterial hypertension. 3. IPF = idiopathic pulmonary fibrosis. 4. IND = investigational new drug. 5. DPI = dry powder inhaler. 6. SMI = soft mist inhaler. 7. PPF = progressive pulmonary fibrosis.
UNITED THERAPEUTICS CORPORATION CONSOLIDATED STATEMENTS OF OPERATIONS (In millions, except per share data) | |||||||
| Three Months Ended June 30, | ||||||
|
| 2026 |
|
|
| 2025 |
|
| (Unaudited) | ||||||
Total revenues | $ | 783.3 |
|
| $ | 798.6 |
|
Operating expenses: |
|
|
| ||||
Cost of sales |
| 99.5 |
|
|
| 87.6 |
|
Research and development |
| 146.3 |
|
|
| 134.0 |
|
Selling, general, and administrative |
| 206.7 |
|
|
| 212.5 |
|
Total operating expenses |
| 452.5 |
|
|
| 434.1 |
|
Operating income |
| 330.8 |
|
|
| 364.5 |
|
Interest income |
| 31.5 |
|
|
| 51.3 |
|
Interest expense |
| (2.9 | ) |
|
| (7.3 | ) |
Other income (expense), net |
| 13.3 |
|
|
| (0.1 | ) |
Total other income, net |
| 41.9 |
|
|
| 43.9 |
|
Income before income taxes |
| 372.7 |
|
|
| 408.4 |
|
Income tax expense |
| (39.7 | ) |
|
| (98.9 | ) |
Net income | $ | 333.0 |
|
| $ | 309.5 |
|
Net income per common share: |
|
|
| ||||
Basic | $ | 7.82 |
|
| $ | 6.86 |
|
Diluted | $ | 7.27 |
|
| $ | 6.41 |
|
Weighted average number of common shares outstanding: |
|
|
| ||||
Basic |
| 42.6 |
|
|
| 45.1 |
|
Diluted |
| 45.8 |
|
|
| 48.3 |
|
SELECTED CONSOLIDATED BALANCE SHEET DATA (Unaudited, in millions) | ||
| June 30,
| |
Cash, cash equivalents, and marketable investments | $ | 3,803.4 |
Total assets |
| 7,220.1 |
Total liabilities |
| 819.8 |
Total stockholders’ equity |
| 6,400.3 |
For Further Information Contact:
Investor Inquiries
https://ir.unither.com/contact-ir
Media Inquiries
[email protected]
Source: United Therapeutics Corporation
Recent Press Releases
29 Jul 2026
United Therapeutics Corporation Announces ADVANCE OUTCOMES Study of Ralinepag Published in The Lancet23 Jul 2026
United Therapeutics Corporation Announces Appointment of Victor Dzau to its Board of Directors
“We just submitted what we believe are two of the most important NDAs in rare pulmonary disease history: ralinepag tablets in PAH and Nebulized Tyvaso in IPF,” said Martine Rothblatt, Ph.D., Chairperson and Chief Executive Officer of United Therapeutics. “We believe that these submissions, accompanied by our planned filings later this year – an IND application for ralinepag DPI and an NDA for treprostinil SMI – may herald an opportunity for a quantum increase in our growth by the end of the decade. By next year, we expect potential approvals for Nebulized Tyvaso in IPF and ralinepag tablets in PAH, two potentially transformative, multi-billion-dollar catalysts that could significantly enhance our growth profile. We expect Tyvaso DPI will then follow Nebulized Tyvaso’s wake into IPF and then PPF. Moreover, our organ manufacturing pipeline continues to advance rapidly with clinical trials ongoing or being planned for liver, kidney, heart, and lung products, and the launch later this year of two xeno-organ production facilities in
“Tyvaso DPI exited the second quarter at record levels of starts, referrals, commercial patients, and total patients, reflecting strong underlying demand,” said Michael Benkowitz, President and Chief Operating Officer of United Therapeutics. “Supported by our competitively differentiated device, deep clinical experience, and significant remaining opportunity in PH-ILD, we are confident in our ability to extend our leadership position in the inhaled prostacyclin class.”
Second Quarter 2026 Financial Results
Key financial highlights include (dollars in millions, except per share data):
| Three Months Ended June 30, |
| Dollar
|
| Percentage
| |||||||
|
| 2026 |
|
| 2025 |
|
| |||||
|
|
|
|
|
|
|
| |||||
Total revenues | $ | 783.3 |
| $ | 798.6 |
| $ | (15.3 | ) |
| (2 | )% |
Net income | $ | 333.0 |
| $ | 309.5 |
| $ | 23.5 |
|
| 8 | % |
Net income, per basic share | $ | 7.82 |
| $ | 6.86 |
| $ | 0.96 |
|
| 14 | % |
Net income, per diluted share | $ | 7.27 |
| $ | 6.41 |
| $ | 0.86 |
|
| 13 | % |
Revenues
The table below presents the components of total revenues (dollars in millions):
| Three Months Ended June 30, |
| Dollar
|
| Percentage
| |||||||
|
| 2026 |
|
| 2025 |
|
| |||||
Net product sales: |
|
|
|
|
|
|
| |||||
Tyvaso DPI® | $ | 326.6 |
| $ | 315.2 |
| $ | 11.4 |
|
| 4 | % |
Nebulized Tyvaso® |
| 126.0 |
|
| 154.4 |
|
| (28.4 | ) |
| (18 | )% |
Total Tyvaso |
| 452.6 |
|
| 469.6 |
|
| (17.0 | ) |
| (4 | )% |
Remodulin®(1) |
| 126.3 |
|
| 134.7 |
|
| (8.4 | ) |
| (6 | )% |
Orenitram® |
| 125.7 |
|
| 123.9 |
|
| 1.8 |
|
| 1 | % |
Unituxin® |
| 65.2 |
|
| 58.4 |
|
| 6.8 |
|
| 12 | % |
Adcirca® |
| 6.7 |
|
| 6.5 |
|
| 0.2 |
|
| 3 | % |
Other |
| 6.8 |
|
| 5.5 |
|
| 1.3 |
|
| 24 | % |
Total revenues | $ | 783.3 |
| $ | 798.6 |
| $ | (15.3 | ) |
| (2 | )% |
(1) | Net product sales include sales of infusion devices, including the Remunity® and RemunityPRO® Pumps. |
Total Tyvaso revenues decreased by four percent to
The table below presents the breakdown of total revenues between
| Three Months Ended June 30, | ||||||||||||||||
| 2026 |
| 2025 | ||||||||||||||
| ROW | Total |
| ROW | Total | ||||||||||||
Net product sales: |
|
|
|
|
|
|
| ||||||||||
Tyvaso DPI | $ | 326.6 | $ | — | $ | 326.6 |
| $ | 314.8 | $ | 0.4 | $ | 315.2 | ||||
Nebulized Tyvaso |
| 109.7 |
| 16.3 |
| 126.0 |
|
| 140.5 |
| 13.9 |
| 154.4 | ||||
Total Tyvaso |
| 436.3 |
| 16.3 |
| 452.6 |
|
| 455.3 |
| 14.3 |
| 469.6 | ||||
Remodulin(1) |
| 99.4 |
| 26.9 |
| 126.3 |
|
| 113.7 |
| 21.0 |
| 134.7 | ||||
Orenitram |
| 125.7 |
| — |
| 125.7 |
|
| 123.9 |
| — |
| 123.9 | ||||
Unituxin |
| 59.0 |
| 6.2 |
| 65.2 |
|
| 55.4 |
| 3.0 |
| 58.4 | ||||
Adcirca |
| 6.7 |
| — |
| 6.7 |
|
| 6.5 |
| — |
| 6.5 | ||||
Other |
| 6.5 |
| 0.3 |
| 6.8 |
|
| 5.0 |
| 0.5 |
| 5.5 | ||||
Total revenues | $ | 733.6 | $ | 49.7 | $ | 783.3 |
| $ | 759.8 | $ | 38.8 | $ | 798.6 | ||||
(1) | Net product sales include sales of infusion devices, including the Remunity and RemunityPRO Pumps. |
Expenses
Cost of sales. The table below summarizes cost of sales by major category (dollars in millions):
| Three Months Ended June 30, |
| Dollar
|
| Percentage
| ||||||
|
| 2026 |
|
| 2025 |
|
| ||||
Category: |
|
|
|
|
|
|
| ||||
Cost of sales | $ | 98.5 |
| $ | 86.6 |
| $ | 11.9 |
| 14 | % |
Share-based compensation expense(1) |
| 1.0 |
|
| 1.0 |
|
| — |
| — | % |
Total cost of sales | $ | 99.5 |
| $ | 87.6 |
| $ | 11.9 |
| 14 | % |
(1) | See Share-based compensationexpense below for discussion. |
Cost of sales, excluding share-based compensation. The increase in cost of sales for the three months ended June 30, 2026, as compared to the same period in 2025, was primarily due to an increase in inventory reserve expense. Of this increased amount,
Research and development expense. The table below summarizes the nature of research and development expense by major expense category (dollars in millions):
| Three Months Ended June 30, |
| Dollar
|
| Percentage
| |||||||
|
| 2026 |
|
| 2025 |
|
| |||||
Category: |
|
|
|
|
|
|
| |||||
External research and development(1) | $ | 71.2 |
| $ | 62.4 |
| $ | 8.8 |
|
| 14 | % |
Internal research and development(2) |
| 54.0 |
|
| 55.9 |
|
| (1.9 | ) |
| (3 | )% |
Share-based compensation expense(3) |
| 10.9 |
|
| 8.1 |
|
| 2.8 |
|
| 35 | % |
Other(4) |
| 10.2 |
|
| 7.6 |
|
| 2.6 |
|
| 34 | % |
Total research and development expense | $ | 146.3 |
| $ | 134.0 |
| $ | 12.3 |
|
| 9 | % |
(1) | External research and development primarily includes fees paid to third parties (such as clinical trial sites, contract research organizations, and contract laboratories) for preclinical and clinical studies and payments to third-party contract manufacturers before regulatory approval of the relevant product. |
(2) | Internal research and development primarily includes salary-related expenses for research and development functions, internal costs to manufacture product candidates before regulatory approval, and internal facilities-related expenses, including depreciation, related to research and development activities. |
(3) | See Share-based compensation expense below for discussion. |
(4) | Other primarily includes upfront fees and milestone payments to third parties under license agreements related to development-stage products and adjustments to the fair value of our contingent consideration obligations. |
Research and development, excluding share-based compensation. The increase in research and development expense for the three months ended June 30, 2026, as compared to the same period in 2025, was primarily due to: (1) an increase in expenditures related to cardiopulmonary treatment projects; and (2) an increase in the fair value of our contingent consideration obligations for manufactured organ and organ alternative projects obtained through acquisition.
Selling, general, and administrative expense. The table below summarizes selling, general, and administrative expense by major category (dollars in millions):
| Three Months Ended June 30, |
| Dollar
|
| Percentage
| |||||||
|
| 2026 |
|
| 2025 |
|
| |||||
Category: |
|
|
|
|
|
|
| |||||
General and administrative(1) | $ | 137.9 |
| $ | 131.1 |
| $ | 6.8 |
|
| 5 | % |
Impairment of property, plant, and equipment (PP&E) |
| — |
|
| 21.7 |
|
| (21.7 | ) |
| (100 | )% |
Sales and marketing |
| 37.3 |
|
| 31.0 |
|
| 6.3 |
|
| 20 | % |
Share-based compensation expense(2) |
| 31.5 |
|
| 28.7 |
|
| 2.8 |
|
| 10 | % |
Total selling, general, and administrative expense | $ | 206.7 |
| $ | 212.5 |
| $ | (5.8 | ) |
| (3 | )% |
(1) | Excluding impairment of PP&E. See Impairment of PP&E section below. |
(2) | See Share-based compensation expense below for discussion. |
General and administrative, excluding impairment of PP&E and share-based compensation. The increase in general and administrative expense for the three months ended June 30, 2026, as compared to the same period in 2025, was primarily due to: (1) an increase in personnel expense due to growth in headcount; and (2) an increase in consulting expenses, partially offset by a decrease in legal expenses related to litigation matters.
Impairment of PP&E. The decrease in impairment of PP&E during the three months ended June 30, 2026, as compared to the same period in 2025, was primarily due to the impairment charge to write down the carrying value of certain PP&E in 2025, which did not recur in 2026.
Sales and marketing, excluding share-based compensation. The increase in sales and marketing expense for the three months ended June 30, 2026, as compared to the same period in 2025, was primarily due to an increase in personnel expense due to growth in headcount.
Share-based compensation expense. The table below summarizes share-based compensation expense by major category (dollars in millions):
| Three Months Ended June 30, |
| Dollar
|
| Percentage
| ||||||
|
| 2026 |
|
| 2025 |
|
| ||||
Category: |
|
|
|
|
|
|
| ||||
Stock options | $ | 12.8 |
| $ | 11.1 |
| $ | 1.7 |
| 15 | % |
Restricted stock units |
| 29.7 |
|
| 26.0 |
|
| 3.7 |
| 14 | % |
Employee stock purchase plan |
| 0.9 |
|
| 0.7 |
|
| 0.2 |
| 29 | % |
Total share-based compensation expense | $ | 43.4 |
| $ | 37.8 |
| $ | 5.6 |
| 15 | % |
Interest income. Interest income was
Other income (expense), net. Other income (expense), net for the three months ended June 30, 2026 and 2025 was
Income tax expense. Income tax expense for the three months ended June 30, 2026 and 2025 was
Share repurchase. In March 2026, our Board of Directors approved a share repurchase program authorizing up to
Webcast
We will host a webcast to discuss our second quarter 2026 financial results on Wednesday, August 5, 2026, at 9:00 a.m. Eastern Time. The webcast can be accessed live via our website at https://ir.unither.com/events-and-presentations. An investor presentation is available now, and after the webcast a replay of the webcast will also be available, at the same location on our website.
About United Therapeutics
Founded by CEO Martine Rothblatt to discover a cure for her daughter's life-threatening rare disease, pulmonary arterial hypertension, United Therapeutics transforms the treatment of rare diseases and pioneers alternatives to expand the supply of transplantable organs. From our innovative therapies to our groundbreaking manufactured organs, we are bold and unconventional. We move quickly from scientific theory to practical technologies that can save lives. As a public benefit corporation, even our legal structure reflects our commitments. We serve patients, act with integrity, create long-term shareholder value, and operate with sustainable practices that protect the future we are working to build.
Forward-Looking Statements
Statements included in this press release that are not historical in nature are “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements include statements related to: our research and development and regulatory plans, including the potential outcome of our NDA and sNDA seeking approval for ralinepag tablets for PAH and Nebulized Tyvaso for IPF, respectively, our plans to submit by the end of this year an IND for ralinepag DPI and an NDA for treprostinil SMI, our plans to develop Tyvaso DPI for IPF and PPF; the potential for us to achieve a quantum increase in our growth by the end of the decade; our expectation that ralinepag tablets and Nebulized Tyvaso for IPF represent multi-billion-dollar catalysts that could significantly enhance our growth profile; our organ manufacturing pipeline, including our planned clinical trials and our plan to launch new xeno-organ facilities later this year; our expectation that our competitively differentiated device, deep clinical experience, and significant remaining opportunity in PH-ILD will enable us to extend our leadership position in the inhaled prostacyclin class; and our goals of expanding the supply of transplantable organs, developing practical technologies that can save lives, creating long-term shareholder value, and operating with sustainable practices. These forward-looking statements are subject to certain risks and uncertainties, such as those described in our periodic reports filed with the Securities and Exchange Commission, that could cause actual results to differ materially from anticipated results. Consequently, such forward-looking statements are qualified by the cautionary statements, cautionary language and risk factors set forth in our periodic reports and documents filed with the Securities and Exchange Commission, including our most recent Annual Report on Form 10-K, Quarterly Reports on Form 10-Q, and Current Reports on Form 8-K. We claim the protection of the safe harbor contained in the Private Securities Litigation Reform Act of 1995 for forward-looking statements. We are providing this information as of August 5, 2026, and assume no obligation to update or revise the information contained in this press release whether as a result of new information, future events, or any other reason.
ORENITRAM, REMODULIN, REMUNITY, REMUNITYPRO, TYVASO, TYVASO DPI, and UNITUXIN are registered trademarks of United Therapeutics Corporation.
ADCIRCA is a registered trademark of Eli Lilly and Company.
Abbreviations:
1. NDA = new drug application. 2. PAH = pulmonary arterial hypertension. 3. IPF = idiopathic pulmonary fibrosis. 4. IND = investigational new drug. 5. DPI = dry powder inhaler. 6. SMI = soft mist inhaler. 7. PPF = progressive pulmonary fibrosis.
UNITED THERAPEUTICS CORPORATION CONSOLIDATED STATEMENTS OF OPERATIONS (In millions, except per share data) | |||||||
| Three Months Ended June 30, | ||||||
|
| 2026 |
|
|
| 2025 |
|
| (Unaudited) | ||||||
Total revenues | $ | 783.3 |
|
| $ | 798.6 |
|
Operating expenses: |
|
|
| ||||
Cost of sales |
| 99.5 |
|
|
| 87.6 |
|
Research and development |
| 146.3 |
|
|
| 134.0 |
|
Selling, general, and administrative |
| 206.7 |
|
|
| 212.5 |
|
Total operating expenses |
| 452.5 |
|
|
| 434.1 |
|
Operating income |
| 330.8 |
|
|
| 364.5 |
|
Interest income |
| 31.5 |
|
|
| 51.3 |
|
Interest expense |
| (2.9 | ) |
|
| (7.3 | ) |
Other income (expense), net |
| 13.3 |
|
|
| (0.1 | ) |
Total other income, net |
| 41.9 |
|
|
| 43.9 |
|
Income before income taxes |
| 372.7 |
|
|
| 408.4 |
|
Income tax expense |
| (39.7 | ) |
|
| (98.9 | ) |
Net income | $ | 333.0 |
|
| $ | 309.5 |
|
Net income per common share: |
|
|
| ||||
Basic | $ | 7.82 |
|
| $ | 6.86 |
|
Diluted | $ | 7.27 |
|
| $ | 6.41 |
|
Weighted average number of common shares outstanding: |
|
|
| ||||
Basic |
| 42.6 |
|
|
| 45.1 |
|
Diluted |
| 45.8 |
|
|
| 48.3 |
|
SELECTED CONSOLIDATED BALANCE SHEET DATA (Unaudited, in millions) | ||
| June 30,
| |
Cash, cash equivalents, and marketable investments | $ | 3,803.4 |
Total assets |
| 7,220.1 |
Total liabilities |
| 819.8 |
Total stockholders’ equity |
| 6,400.3 |
For Further Information Contact:
Investor Inquiries
https://ir.unither.com/contact-ir
Media Inquiries
[email protected]
Source: United Therapeutics Corporation
Recent Press Releases
29 Jul 2026
United Therapeutics Corporation Announces ADVANCE OUTCOMES Study of Ralinepag Published in The Lancet23 Jul 2026
United Therapeutics Corporation Announces Appointment of Victor Dzau to its Board of Directors
决策记录链 · 只追加
每次领取产生一条记录,重新决策追加一条并以 supersedes 指向被替代的记录(ADR 0014)。
这条决策早于决策账本(2026-10-08 起逐条追加),没有追加记录。