Neurocrine Biosciences Reports Second-Quarter 2026 Financial Results
Rhea-AI Summary
Neurocrine Biosciences (Nasdaq: NBIX) reported second-quarter 2026 total revenue of $959 million, up 39% year-over-year, with net product sales of INGREZZA at $716 million (+15%), CRENESSITY at $184 million (+247%), and VYKAT XR at $54 million from the May 18 Soleno acquisition close. Unaudited pro-forma total revenue including a full quarter of VYKAT XR was $998 million.
GAAP net income was $144 million (diluted EPS $1.39) versus $108 million ($1.06) a year ago; Non-GAAP net income was $297 million (EPS $2.85) versus $166 million ($1.65). Cash, cash equivalents, and marketable securities were $482 million at June 30, 2026, compared with $2.543 billion at year-end 2025. Full-year 2026 INGREZZA net sales guidance increased to $2.825–$2.875 billion, while GAAP R&D, GAAP SG&A, and amortization guidance rose, reflecting portfolio investment and Soleno-related intangible amortization.
Positive
- Total revenue up 39% YoY to $959 million in Q2 2026
- INGREZZA net sales grew 15% YoY to $716 million in Q2
- CRENESSITY net sales rose to $184 million, up 247% YoY
- Added VYKAT XR with Q2 net sales of $54 million post-close; pro-forma $94 million
- Non-GAAP diluted EPS increased to $2.85 from $1.65 year-over-year
- INGREZZA 2026 guidance raised to $2.825–$2.875 billion in net sales
- Completed $2.9 billion Soleno acquisition adding PWS hyperphagia therapy VYKAT XR
- Established a $1.0 billion senior secured revolving credit facility with full availability
Negative
- Cash, cash equivalents, and marketable securities declined to $482 million from $2.543 billion at year-end 2025
- GAAP R&D expense guidance raised to $1.275–$1.325 billion for 2026
- GAAP SG&A guidance increased to $1.575–$1.600 billion for 2026
- New amortization of acquired intangibles guided at $85–$90 million for 2026
- Q2 2026 GAAP SG&A expense rose to $440 million from $286 million year-over-year
- Q2 2026 GAAP R&D expense increased to $327 million from $244 million a year earlier
News Explained
The May cash acquisition added VYKAT XR; a new $1 billion facility provides borrowing capacity for general corporate purposes.
The Soleno Therapeutics acquisition closed on
The disclosed consideration specifies a cash-funded acquisition, while the release does not describe an equity issuance as part of that consideration.
Separately, Neurocrine entered a
The acquisition added approximately
Key Figures
Previous Earnings Reports
| Date | Event | Sentiment | 24h Move | Catalyst |
|---|---|---|---|---|
| May 05 | First-quarter earnings | Positive | +8.9% | Revenue growth, higher earnings, Soleno acquisition agreement, and reaffirmed INGREZZA guidance |
| Feb 11 | Fourth-quarter earnings | Positive | -10.4% | Quarterly sales growth and 2026 INGREZZA guidance accompanied increased investment expectations |
| Oct 28 | Third-quarter earnings | Positive | -6.3% | Sales growth, product demand, and reaffirmed annual INGREZZA guidance |
| Jul 30 | Second-quarter earnings | Positive | -6.2% | Sales growth, narrowed guidance, pipeline progress, and share repurchases |
| May 05 | First-quarter earnings | Positive | +8.4% | INGREZZA growth, reaffirmed guidance, pipeline progress, and completed share repurchase |
24h Move is the share-price change in the day after each event; other market factors may also have contributed.
Earnings-tagged history showed positive reported fundamentals but price-reaction divergence in three of five events; the average move was -1.16%.
Key Terms
non-gaap financial
phase 3 medical
pro-forma financial
senior secured revolving credit facility financial
hyperphagia medical
AI-generated analysis. How Rhea-AI works. Not financial advice.
Total Second-Quarter 2026 Revenue Grew
INGREZZA® (valbenazine) 2026 Net Sales Guidance Raised to
Acquisition of Soleno Therapeutics Completed in May 2026
"Our second quarter performance demonstrates the power of a strategy designed to compound over time," said Kyle W. Gano, Ph.D., Chief Executive Officer of Neurocrine Biosciences. "As our commercial portfolio of first-in-class medicines continues to grow, so does our capacity to reinvest in innovation, advance a differentiated late-stage pipeline and pursue strategic opportunities that strengthen the company for the long term. With multiple important clinical milestones in 2027, including Phase 3 readouts for osavampator in major depressive disorder and direclidine in schizophrenia, we are building an enduring company poised to deliver meaningful value for patients and shareholders for years to come."
Total Revenue Highlights
Three Months Ended June 30, | |||||
(unaudited, in millions, except per share data) | 2026 | 2025 | YoY Growth | ||
Revenues: | |||||
INGREZZA Net Product Sales | $ 716 | $ 624 | 15 % | ||
CRENESSITY® (crinecerfont) Net Product Sales | 184 | 53 | 247 % | ||
VYKAT® (diazoxide choline) XR Net Product Sales* | 54 | — | NM | ||
Other Revenues | 5 | 11 | NM | ||
Total Revenues | $ 959 | $ 688 | 39 % | ||
* Net product sales for VYKAT XR are included from the closing of the Soleno Therapeutics acquisition on May 18th |
- Total revenues for the second quarter 2026 were
$959 million $688 million 39% year-over-year growth. Unaudited pro-forma total revenues were$998 million - INGREZZA second-quarter 2026 net product sales were
$716 million 15% growth year-over-year. Results reflected double-digit prescription volume growth in TRx and record NRx driven by strong patient demand. - INGREZZA full year 2026 guidance was increased from a range of
$2.7 billion $2.8 billion $2.825 billion $2.875 billion - CRENESSITY second-quarter 2026 net product sales were
$184 million 80% reimbursement for dispensed prescriptions in the second quarter 2026. - VYKAT XR second-quarter 2026 net product sales were
$54 million $94 million
Recent Clinical and Corporate Developments
- In May 2026, acquired Soleno Therapeutics for
$53.00 $2.9 billion - In May 2026, the Company entered into a
$1.0 billion $1.0 billion - Announced new two-year data from the Phase 3 CAHtalyst® Pediatric study showing positive growth outcomes in children and adolescents with classic congenital adrenal hyperplasia treated with CRENESSITY.
- Announced new two-year data from the Phase 3 CAHtalyst® Adult study demonstrating improved cardiometabolic outcomes alongside sustained glucocorticoid dose reduction through up to two years of treatment with CRENESSITY for classic congenital adrenal hyperplasia.
- Announced publication of expert recommendations for glucocorticoid dose reduction after initiating CRENESSITY for the treatment of classic congenital adrenal hyperplasia.
- Presented new VYKAT XR data demonstrating meaningful and durable improvements in hyperphagia and behavioral symptoms in Prader-Willi syndrome following randomized withdrawal period.
- Announced new post-hoc data from the KINECT® 4 clinical trial demonstrating that adults with tardive dyskinesia treated with INGREZZA capsules experienced clinically meaningful and robust improvements in involuntary movement severity, including those who did not meet the stringent symptomatic remission threshold.
- Initiated Phase 2 clinical study to assess the safety and tolerability of crinecerfont in children aged 3 months to under 4 years with classic congenital adrenal hyperplasia.
- Promoted Samir Siddhanti to the executive management team as Chief Business Officer where he will lead the Company's business development, corporate strategy, and R&D portfolio management functions helping guide Neurocrine's continued evolution into a leading, global biotechnology company.
Second-Quarter 2026 Financial Results
Three Months Ended June 30, | |||
(unaudited, in millions, except per share data) | 2026 | 2025 | |
Total Revenues | $ 959 | $ 688 | |
GAAP Cost of Revenues | $ 23 | $ 10 | |
Non-GAAP Cost of Revenues | $ 18 | $ 10 | |
GAAP Research and Development (R&D) | $ 327 | $ 244 | |
Non-GAAP R&D | $ 276 | $ 223 | |
GAAP Selling, General, and Administrative (SG&A) | $ 440 | $ 286 | |
Non-GAAP SG&A | $ 305 | $ 255 | |
GAAP Net Income | $ 144 | $ 108 | |
GAAP Earnings Per Share – Diluted | $ 1.39 | $ 1.06 | |
Non-GAAP Net Income | $ 297 | $ 166 | |
Non-GAAP Earnings Per Share – Diluted | $ 2.85 | $ 1.65 | |
(unaudited, in millions) | June 30, 2026 | December 31, 2025 | |
Total Cash, Cash Equivalents, and Marketable Securities | $ 482 | $ 2,543 | |
- Second-quarter 2026 GAAP net income and earnings per share were
$144 million $1.39 $108 million $1.06 - Second-quarter 2026 Non-GAAP net income and earnings per share were
$297 million $2.85 $166 million $1.65 - A reconciliation of GAAP to Non-GAAP financial results can be found in Table 3 at the end of this press release.
- Second-quarter 2026 GAAP and Non-GAAP net income compared with second-quarter 2025 were primarily driven by:
- Higher net product sales of
$272 million - For the second quarter 2026, GAAP operating expenses included certain expenses associated with the acquisition of Soleno Therapeutics, Inc., which closed in May 2026, and are excluded from Non-GAAP operating expenses.
- Increased R&D expense in support of an expanded and advancing pre-clinical and clinical portfolio included investments in the osavampator Phase 3 program in major depressive disorder (MDD) and the muscarinic franchise, including the direclidine Phase 3 program as a potential treatment for adults with schizophrenia. Development milestone expense included in R&D was
$0.3 million $15 million - Increased SG&A expense primarily reflected continued investment in our commercial organization, included the expansion of our INGREZZA and CRENESSITY sales teams in the first quarter of 2026 and partial quarter of expense for support of VYKAT XR.
- Higher net product sales of
- At June 30, 2026, the Company had cash, cash equivalents, and marketable securities totaling approximately
$482 million .
Full Year 2026 Financial Guidance
(dollars in millions) | Prior | Updated | |
INGREZZA Net Product Sales 1 | |||
GAAP R&D 2 | |||
Non-GAAP R&D 2, 3 | |||
IPR&D 4 | |||
GAAP SG&A 5 | |||
Non-GAAP SG&A 3, 5 | |||
GAAP Amortization of Acquired | Not applicable |
- INGREZZA sales guidance reflects expected net product sales of INGREZZA in tardive dyskinesia and chorea associated with Huntington's disease.
- R&D guidance reflects the continued advancement of the Company's pre-clinical and clinical portfolio including the Phase 3 programs for osavampator in MDD and direclidine in schizophrenia, and includes approximately
$25 million - Non-GAAP guidance has been adjusted to exclude estimated non-cash stock-based compensation expense of approximately
$115 million $170 million $58 million $95 million - IPR&D guidance represents completed collaboration and licensing arrangements.
- SG&A guidance reflects expense for ongoing commercial initiatives, including the recent expansion of our sales teams in Q1 2026, supporting INGREZZA growth and the launch of CRENESSITY and VYKAT XR.
- In connection with the acquisition of Soleno, the Company recorded approximately
$2.2 billion
Conference Call and Webcast Today at 4:30 PM Eastern Time
Neurocrine Biosciences will hold a live conference call and webcast today at 4:30 p.m. Eastern Time (1:30 p.m. Pacific Time). Participants can access the live conference call by dialing 800-347-6865 (US) or 203-518-9757 (International) using the conference ID: NBIX. The webcast and accompanying slides can also be accessed at approximately 4:30 p.m. Eastern Time on Neurocrine Biosciences' website under Investors at www.neurocrine.com. A replay of the webcast will be available on the website approximately one hour after the conclusion of the event and will be archived for approximately one month.
About Neurocrine Biosciences
Neurocrine Biosciences is a leading biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering, developing and commercializing life-changing treatments for patients with under-addressed neurological, psychiatric, endocrine and immunological disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, hyperphagia in Prader-Willi syndrome, endometriosis* and uterine fibroids*, as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For more than three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders, because you deserve brave science. For more information, visit neurocrine.com, and follow the company on LinkedIn, X, Facebook and YouTube. (*in collaboration with AbbVie)
NEUROCRINE, the NEUROCRINE BIOSCIENCES Logo, YOU DESERVE BRAVE SCIENCE, INGREZZA, and CRENESSITY are registered trademarks of Neurocrine Biosciences, Inc. VYKAT is a registered trademark of Soleno Therapeutics, Inc.
Non-GAAP Financial Measures
In addition to the financial results and financial guidance that are provided in accordance with accounting principles generally accepted in the United States (GAAP), this press release also contains the following Non-GAAP financial measures: Non-GAAP cost of revenues, Non-GAAP R&D expense, Non-GAAP SG&A expense, Non-GAAP other income (expense), net, Non-GAAP net income and earnings per share. When preparing the Non-GAAP financial results and guidance, the Company excludes certain GAAP items that management does not consider to be normal, including recurring cash operating expenses that might not meet the definition of unusual or non-recurring items. In particular, these Non-GAAP financial measures exclude: non-cash stock-based compensation expense, amortization expense related to acquired intangible assets, amortization expense related to acquisition-date inventory fair value step-up, stock based compensation expense related to the acceleration of vesting of equity awards for Soleno employees, changes in fair value of equity investments, acquisition-related transaction and integration costs, gains on sales of businesses, net of transaction costs, other divestiture-related transaction costs, changes in foreign currency exchange rates and certain adjustments to income tax expense. These Non-GAAP financial measures are provided as a complement to results provided in accordance with GAAP as management believes these Non-GAAP financial measures are useful to investors because they help indicate underlying trends in the Company's business, are important in comparing current results with prior period results and provide additional information regarding the Company's financial position. Management also uses these Non-GAAP financial measures to establish budgets and operational goals that are communicated internally and externally and to manage the Company's business and evaluate its performance. The Company provides guidance regarding combined R&D and SG&A expenses on both a GAAP and a Non-GAAP basis. A reconciliation of these GAAP financial results to Non-GAAP financial results is included in the attached financial information.
In connection with the Soleno acquisition, this press release also includes unaudited pro forma full quarter VYKAT XR net product sales and total revenue, Non-GAAP financial measures, which management uses, and believes is useful to investors, to provide supplemental information regarding VYKAT XR net product sales for the full second quarter of 2026, including the period from April 1, 2026 through May 17, 2026, prior to the closing of the acquisition on May 18, 2026.
Forward-Looking Statements
In addition to historical facts, this press release contains forward-looking statements that involve a number of risks and uncertainties. These statements include, but are not limited to, statements related to: our business strategy, objectives, and future development plans; the benefits to be derived from our products and product candidates; the value our products and/or our product candidates may bring to patients; the continued success of INGREZZA; successfully commercializing CRENESSITY and VYKAT XR; our financial and operating performance, including our future revenues, expenses, or profits; our full year 2026 financial guidance; our acquisition of Soleno Therapeutics, including the prospective benefits of the acquisition, and our strategy, plans, objectives, expectations (financial or otherwise) and intentions with respect to our future financial results, growth potential and anticipated product portfolio in connection with the acquisition; our collaborative partnerships; clinical and scientific data updates for our products and product candidates, including observations regarding clinical outcomes, safety, and tolerability; expected future clinical and regulatory milestones; and the timing of the initiation and/or completion of our clinical, regulatory, and other development activities and those of our collaboration partners. Factors that could cause actual results to differ materially from those stated or implied in the forward-looking statements, include but are not limited to the following: risks and uncertainties associated with Neurocrine Biosciences' business and finances in general; risks and uncertainties associated with the commercialization of our products; risks related to our ability to realize the anticipated benefits of the acquisition of Soleno Therapeutics, including the possibility that the expected benefits from the acquisition will not be realized or will not be realized within the expected time period and that we will not be able to integrate Soleno Therapeutics' business successfully or that such integration may be more difficult, time-consuming or costly than expected, disruption from the acquisition, making it more difficult to conduct business as usual or maintain relationships with employees, customers, suppliers, other business partners or governmental entities, unknown or inestimable liabilities, the risk of litigation and/or regulatory actions related to the acquisition, and the degree and pace of market uptake of VYKAT XR; risks related to the development of our product candidates; risks associated with our dependence on third parties for development, manufacturing, and commercialization activities for our products and product candidates, and our ability to manage these third parties; risks that the FDA or other regulatory authorities may make adverse decisions regarding our products or product candidates; risks that development activities may not be initiated or completed on time or at all, or may be delayed for regulatory, manufacturing, or other reasons, may not be successful or replicate previous clinical trial results, may fail to demonstrate that our product candidates are safe and effective, or may not be predictive of real-world results or of results in subsequent clinical trials; risks that the potential benefits of the agreements with our collaboration partners may never be realized; risks that our products, and/or our product candidates may be precluded from commercialization by the proprietary or regulatory rights of third parties, or have unintended side effects, adverse reactions or incidents of misuse; risks associated with government and third-party regulatory and/or policy efforts which may, among other things, impose sales and pharmaceutical pricing controls on our products or limit coverage and/or reimbursement for our products; risks associated with competition from other therapies or products, including potential generic entrants for our products; risks associated with our ability to manage the growth of our organization; and other risks described in our periodic reports filed with the Securities and Exchange Commission. Neurocrine Biosciences disclaims any obligation to update the statements contained in this press release after the date hereof other than as required by law.
TABLE 1 | |||||||
NEUROCRINE BIOSCIENCES, INC. | |||||||
Three Months Ended | Six Months Ended | ||||||
2026 | 2025 | 2026 | 2025 | ||||
Revenues: | |||||||
Net product sales | $ 954.3 | $ 682.0 | $ 1,765.3 | $ 1,245.7 | |||
Collaboration revenues | 4.7 | 5.5 | 8.2 | 14.4 | |||
Total revenues | 959.0 | 687.5 | 1,773.5 | 1,260.1 | |||
Operating expenses: | |||||||
Cost of revenues, excluding amortization of acquired intangible assets | 23.2 | 10.3 | 36.9 | 18.5 | |||
Research and development | 326.7 | 244.3 | 622.9 | 507.5 | |||
Acquired in-process research and development | 1.5 | — | 22.7 | 0.1 | |||
Selling, general, and administrative | 439.7 | 286.3 | 758.2 | 562.8 | |||
Amortization of acquired intangible assets | 16.4 | 1.0 | 16.5 | 2.0 | |||
Gain on sale of business, net of transaction costs | — | — | (28.6) | — | |||
Total operating expenses | 807.5 | 541.9 | 1,428.6 | 1,090.9 | |||
Operating income | 151.5 | 145.6 | 344.9 | 169.2 | |||
Other income (expense): | |||||||
Interest expense | (2.9) | — | (2.9) | — | |||
Unrealized gain (loss) on equity investments | 1.2 | (6.7) | 26.5 | (37.3) | |||
Investment income and other, net | 12.4 | 20.6 | 40.5 | 42.3 | |||
Total other income (expense), net | 10.7 | 13.9 | 64.1 | 5.0 | |||
Income before provision for income taxes | 162.2 | 159.5 | 409.0 | 174.2 | |||
Provision for income taxes | 17.8 | 52.0 | 66.7 | 58.8 | |||
Net income | $ 144.4 | $ 107.5 | $ 342.3 | $ 115.4 | |||
Earnings per share, basic | $ 1.43 | $ 1.09 | $ 3.40 | $ 1.16 | |||
Earnings per share, diluted | $ 1.39 | $ 1.06 | $ 3.30 | $ 1.13 | |||
Weighted average common shares outstanding, basic | 101.0 | 99.0 | 100.8 | 99.3 | |||
Weighted average common shares outstanding, diluted | 104.2 | 101.0 | 103.8 | 101.8 | |||
TABLE 2 | |||
NEUROCRINE BIOSCIENCES, INC. | |||
June 30, 2026 | December 31, 2025 | ||
Cash, cash equivalents, and marketable securities | $ 389.8 | $ 1,480.4 | |
Accounts receivable | 887.0 | 686.8 | |
Inventory | 104.2 | 69.0 | |
Other current assets | 256.5 | 286.5 | |
Total current assets | 1,637.5 | 2,522.7 | |
Noncurrent inventory | 149.1 | — | |
Noncurrent marketable securities | 91.9 | 1,063.0 | |
Right-of-use assets | 448.0 | 455.4 | |
Equity investments | 147.3 | 120.8 | |
Property and equipment, net | 90.5 | 89.8 | |
Intangible assets, net | 2,226.0 | 4.7 | |
Goodwill | 500.6 | 6.1 | |
Deferred tax assets | 8.9 | 320.3 | |
Other noncurrent assets | 59.3 | 48.7 | |
Total assets | $ 5,359.1 | $ 4,631.5 | |
Total current liabilities | 874.5 | 743.4 | |
Deferred tax liabilities | 91.5 | — | |
Noncurrent operating lease liabilities | 401.8 | 415.3 | |
Other noncurrent liabilities | 297.7 | 219.7 | |
Stockholders' equity | 3,693.6 | 3,253.1 | |
Total liabilities and stockholders' equity | $ 5,359.1 | $ 4,631.5 | |
TABLE 3 | |||||||
NEUROCRINE BIOSCIENCES, INC. | |||||||
Three Months Ended | Six Months Ended | ||||||
2026 | 2025 | 2026 | 2025 | ||||
GAAP net income 1 | $ 144.4 | $ 107.5 | $ 342.3 | $ 115.4 | |||
Adjustments: | |||||||
Stock-based compensation expense | 65.0 | 52.8 | 122.2 | 105.6 | |||
Acceleration of stock-based compensation expense and related taxes 2 | 60.1 | — | 60.1 | — | |||
Acquisition-related employee compensation and severance costs | 21.9 | — | 21.9 | — | |||
Amortization of inventory fair value step-up 3 | 3.0 | — | 3.0 | — | |||
Amortization of acquired intangible assets 4 | 16.4 | 1.0 | 16.5 | 2.0 | |||
Acquisition/divestiture-related transaction and integration costs | 45.0 | — | 48.7 | — | |||
Gain on sale of business, net of transaction costs 5 | — | — | (28.6) | — | |||
Changes in fair values of equity investments 6 | (1.2) | 6.7 | (26.5) | 37.3 | |||
Other | 0.7 | 0.8 | 1.3 | 2.3 | |||
Income tax effect related to reconciling items 7 | (58.6) | (2.6) | (63.7) | (24.8) | |||
Non-GAAP net income 1 | $ 296.7 | $ 166.2 | $ 497.2 | $ 237.8 | |||
Diluted earnings per share: | |||||||
GAAP | $ 1.39 | $ 1.06 | $ 3.30 | $ 1.13 | |||
Non-GAAP | $ 2.85 | $ 1.65 | $ 4.79 | $ 2.34 | |||
Three Months Ended | Six Months Ended | ||||||
2026 | 2025 | 2026 | 2025 | ||||
Cost of Revenues: | |||||||
GAAP cost of revenues | $ 23.2 | $ 10.3 | $ 36.9 | $ 18.5 | |||
Adjustments: | |||||||
Acceleration of stock-based compensation expense and related taxes 2 | 1.8 | — | 1.8 | — | |||
Acquisition-related employee compensation and severance costs | 0.2 | — | 0.2 | — | |||
Amortization of inventory fair value step-up 3 | 3.0 | — | 3.0 | — | |||
Non-GAAP cost of revenues | $ 18.2 | $ 10.3 | $ 31.9 | $ 18.5 | |||
Research and Development: | |||||||
GAAP R&D | $ 326.7 | $ 244.3 | $ 622.9 | $ 507.5 | |||
Adjustments: | |||||||
Stock-based compensation expense | 27.5 | 21.6 | 51.7 | 44.6 | |||
Acceleration of stock-based compensation expense and related taxes 2 | 18.1 | — | 18.1 | — | |||
Acquisition-related employee compensation and severance costs | 5.0 | — | 5.0 | — | |||
Non-GAAP R&D | $ 276.1 | $ 222.7 | $ 548.1 | $ 462.9 | |||
Selling, General, and Administrative: | |||||||
GAAP SG&A | $ 439.7 | $ 286.3 | $ 758.2 | $ 562.8 | |||
Adjustments: | |||||||
Stock-based compensation expense | 37.5 | 31.2 | 70.5 | 61.0 | |||
Acceleration of stock-based compensation expense and related taxes 2 | 40.2 | — | 40.2 | — | |||
Acquisition-related employee compensation and severance costs | 16.7 | — | 16.7 | — | |||
Acquisition/divestiture-related transaction and integration costs | 39.9 | — | 43.6 | — | |||
Other | 0.5 | 0.5 | 1.1 | 1.9 | |||
Non-GAAP SG&A | $ 304.9 | $ 254.6 | $ 586.1 | $ 499.9 | |||
Amortization of Acquired Intangible Assets: | |||||||
GAAP amortization of acquired intangible assets | $ 16.4 | $ 1.0 | $ 16.5 | $ 2.0 | |||
Adjustments: | |||||||
Amortization of acquired intangible assets 4 | 16.4 | 1.0 | 16.5 | 2.0 | |||
Non-GAAP amortization of acquired intangible assets | $ — | $ — | $ — | $ — | |||
Gain on Sale of Business, Net of Transaction Costs: | |||||||
GAAP gain on sale of business, net of transaction costs | $ — | $ — | $ (28.6) | $ — | |||
Adjustments: | |||||||
Gain on sale of business, net of transaction costs 5 | — | — | (28.6) | — | |||
Non-GAAP gain on sale of business, net of transaction costs | $ — | $ — | $ — | $ — | |||
Other Income (Expense): | |||||||
GAAP other income, net | $ 10.7 | $ 13.9 | $ 64.1 | $ 5.0 | |||
Adjustments: | |||||||
Changes in fair values of equity investments 6 | (1.2) | 6.7 | (26.5) | 37.3 | |||
Acquisition/divestiture-related transaction and integration costs | 5.1 | — | 5.1 | — | |||
Other | 0.2 | 0.3 | 0.2 | 0.4 | |||
Non-GAAP other income, net | $ 14.8 | $ 20.9 | $ 42.9 | $ 42.7 | |||
1. | Includes the following expenses: |
Three Months Ended | Six Months Ended | ||||||
2026 | 2025 | 2026 | 2025 | ||||
Milestones (R&D) | $ 0.3 | $ 15.1 | $ 22.9 | $ 60.5 | |||
Acquired in-process research and development (IPR&D) | $ 1.5 | $ — | $ 22.7 | $ 0.1 | |||
2. | Relates to the acceleration of vesting of equity awards for Soleno employees which vested in full upon the closing of the transaction. |
3. | Relates to amortization expense associated with recording approximately |
4. | Primarily relates to amortization of acquired intangible assets associated with the recording of approximately |
5. | Reflects a pre-tax gain, net of transaction costs, recognized on the sale of Neurocrine Group Limited in January 2026. |
6. | Reflects periodic fluctuations in the fair values of equity investments. |
7. | Estimated income tax effect of Non-GAAP reconciling items are calculated using applicable statutory tax rates, taking into consideration any valuation allowance. In addition, Non-GAAP tax expense may also be affected by certain non-recurring, non-operating, or discrete tax items. |
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SOURCE Neurocrine Biosciences, Inc.