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Schr dinger Reports Second Quarter 2025 Financial Results Second Quarter Total Revenue of $54.8 Million, Software Revenue of $40.5 Million Maintains Full Year 2025 Revenue Growth Guidance and Lowers Operating Expense Gui

Key Takeaway: Schr dinger Reports Second Quarter 2025 Financial Results Second Quarter Total Revenue of $54.8 Million, Software Revenue of $40.5 Million Maintains Full Year 2025 Revenue Growth Guidance and Lowers Operating Expense Guidance Company to Complete Phase 1 Data Package for SGR-15

Full Press Release Details

Schr dinger Reports Second Quarter 2025 Financial Results
Second Quarter Total Revenue of $54.8 Million, Software Revenue of $40.5 Million
Maintains Full Year 2025 Revenue Growth Guidance and Lowers Operating Expense Guidance
Company to Complete Phase 1 Data Package for SGR-1505 While Exploring Strategic Opportunities for Clinical Development
Initial Clinical Data for SGR-3515 and SGR-2921 Expected in Fourth Quarter of 2025
New York, August 6, 2025 - Schr dinger, Inc. (Nasdaq SDGR) today announced financial results for the quarter ended June 30, 2025.
In a highly dynamic macroenvironment, our ability to deliver solid second quarter results and maintain our 2025 revenue growth guidance is a testament to our strong customer relationships and the demand for proven computational technologies to accelerate molecular discovery," said Ramy Farid, Ph.D., chief executive officer of Schr dinger. "In addition to progressing several collaborative programs in our pipeline, we achieved an important milestone with the presentation of encouraging initial data for our MALT1 inhibitor, SGR-1505, and we expect to report initial data from our other two clinical programs in the fourth quarter."
Earlier this year, Schr dinger presented initial Phase 1 data for SGR-1505 in patients with relapsed refractory B-cell malignancies. SGR-1505 was observed to be well tolerated and clinically active with responses observed in multiple histologies, including in patients with chronic lymphocytic leukemia and Waldenstr m macroglobulinemia.
"We are very pleased with the initial Phase 1 SGR-1505 data we presented last month at EHA and ICML. We are exploring strategic opportunities for SGR-1505 with the goals of accelerating the clinical development of this potential best-in-class molecule and maximizing benefit to patients globally," stated Karen Akinsanya, Ph.D., president, head of therapeutics R D and chief strategy officer, partnerships. "In parallel, we plan to complete the Phase 1 package and meet with the FDA later this year to discuss the recommended Phase 2 dose."
Second Quarter 2025 Financial Results
Total revenue for the second quarter increased 16% to $54.8 million, compared to $47.3 million in the second quarter of 2024.
Software revenue for the second quarter increased 15% to $40.5 million, compared to $35.4 million in the second quarter of 2024. The increase was primarily due to increases in revenue recognized from hosted contracts and contribution revenue, partially offset by revenue from multi-year on-premise contracts signed in the prior year.
Drug discovery revenue was $14.2 million for the second quarter, compared to $11.9 million in the second quarter of 2024.
Software gross margin was 68% for the second quarter, compared to 80% in the second quarter of 2024, primarily reflecting the costs associated with the company's predictive toxicology initiative.
Operating expenses were $79.1 million for the second quarter, compared to $84.1 million for the second quarter of 2024. The decrease was due to lower R D expenses.
Other income was $10.0 million for the second quarter, which included changes in fair value of equity investments and interest income expense, compared to other expense of $1.2 million for the second quarter of 2024.
Net loss for the second quarter was $43.2 million, compared to $54.0 million in the second quarter of 2024.
Three Months Ended
June 30,
2025 2024 % Change
(in millions)
Total revenue $ 54.8 $ 47.3 16%
Software revenue 40.5 35.4 15%
Drug discovery revenue 14.2 11.9 19%
Software gross margin 68 % 80 %
Operating expenses $ 79.1 $ 84.1 (6.0)%
Other income (expense) $ 10.0 $ (1.2) -
Net loss $ (43.2) $ (54.0) -
For the three and six months ended June 30, 2025, Schr dinger reported a non-GAAP net loss of $47.5 million and $94.2 million, compared to a non-GAAP net loss of $48.1 million and $110.5 million for the three and six months ended June 30, 2024. See "Non-GAAP Information" below and the table at the end of this press release for a reconciliation of non-GAAP net loss to GAAP net loss.
2025 Financial Outlook
As of August 6, 2025, Schr dinger updated its expectation for operating expenses and reaffirmed the other aspects of its previously issued financial guidance for the fiscal year ending December 31, 2025
Software revenue growth is expected to range from 10% to 15%.
Drug discovery revenue is expected to range from $45 million to $50 million.
Software gross margin is expected to range from 74% to 75%.
Operating expenses in 2025 are now expected to be lower than 2024.
Cash used for operating activities in 2025 is expected to be significantly lower than cash used for operating activities in 2024.
For the third quarter of 2025, software revenue is expected to range from $36 million to $40 million.
Proprietary and Collaborative Pipeline
In June, Schr dinger presented encouraging initial Phase 1 clinical data for SGR-1505, the company's MALT1 inhibitor in patients with relapsed refractory B-cell malignancies. These data were presented at the European Hematology Association Annual Congress and International Conference on Malignant Lymphoma. Also in June, SGR-1505 received Fast Track Designation from the FDA for the treatment of adult patients with Waldenstr m macroglobulinemia that have failed at least two lines of therapy, including a Bruton's tyrosine kinase (BTK) inhibitor. Schr dinger is completing the Phase 1 package and expects to meet with the FDA later this year to discuss the recommended Phase 2 dose. The company is also exploring strategic opportunities to advance the development of SGR-1505.
Schr dinger is continuing to progress the Phase 1 clinical study of SGR-2921, the company's CDC7 inhibitor, in patients with acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS). Initial clinical data from this study are expected in the fourth quarter of 2025.
Schr dinger is continuing to progress the Phase 1 clinical study of SGR-3515, the company's Wee1 Myt1 co-inhibitor, in patients with advanced solid tumors. Initial clinical data from this study are expected in the fourth quarter of 2025.
In July, Schr dinger announced an expanded research collaboration with Ajax Therapeutics, a company co-founded by Schr dinger. The expansion adds a new Janus kinase (JAK) target to the collaboration. Under the terms of the amended collaboration agreement, Schr dinger is eligible to receive discovery and development milestones for the new target similar to the terms of the original collaboration agreement. Schr dinger is also eligible to receive sales milestones and single-digit royalties on net sales of any products emerging from the additional target.
Scientists at Schr dinger, Sanofi, Galapagos and UCB published an industry perspective on computational hit-finding in the Journal of Medicinal Chemistry. The paper highlights how recent breakthroughs in computational power, AI, and expansive chemical libraries are reshaping virtual screening and hit identification, and emphasizes the importance of accurate physics-based methods, including Schr dinger's FEP+.
In May, the company completed a review of the organization and implemented several changes to improve its operating expense profile and reduce cash burn, including a reduction in force of approximately 7% of full-time employees, which is expected to reduce operating expenses by approximately $30 million on an annualized basis. Separately, Schr dinger announced the appointment of Richie Jain to chief financial officer, the addition of Mannix Aklian as chief commercial officer, global head of software sales and marketing, and the expansion of Karen Akinsanya's role to president, head of therapeutics R D and chief strategy officer, partnerships.
Webcast and Conference Call Information
Schr dinger will host a conference call to discuss its second quarter 2025 financial results on Wednesday, August 6, 2025, at 4 30 p.m. ET. The live webcast can be accessed under "News Events" in the investors section of Schr dinger's website, https ir.schrodinger.com news-and-events event-calendar. To participate in the live call, please register for the call here. It is recommended that participants register at least 15 minutes in advance of the call. Once registered, participants will receive the dial-in information. The archived webcast will be available on Schr dinger's website for approximately 90 days following the event.
Non-GAAP Information
Included in this press release is certain financial information that has not been prepared in accordance with generally accepted accounting principles in the United States (GAAP). The company presents non-GAAP net income (loss) and non-GAAP net income (loss) per share, which exclude gains and losses on equity investments, changes in fair value of equity investments, and income tax benefits and expenses. Adjusting net income to exclude the impact of these items results in a financial presentation for the company without the impact of our equity investments and tax benefits and expenses. Management believes non-GAAP net income (loss) and non-GAAP net income (loss) per share are useful measures for investors, taken in conjunction with the company's GAAP financial statements because they provide greater period-over-period comparability with respect to the company's operating performance, by excluding non-cash mark-to-market and other valuation adjustments for the company's equity investments, non-recurring cash distributions from the company's equity investments and the tax impact of these distributions that are not reflective of the ongoing operating performance of the business. However, the non-GAAP measures should be considered only in addition to, not
as a substitute for or as superior to, net income (loss) and net income (loss) per share or other financial measures prepared in accordance with GAAP.
Other companies in Schr dinger's industry may calculate non-GAAP net income (loss) and non-GAAP net income (loss) per share, differently than we do, limiting their usefulness as comparative measures. For a reconciliation of non-GAAP net income (loss) and non-GAAP net income (loss) per share to GAAP net income (loss) and GAAP net income (loss) per share, respectively, please refer to the tables at the end of this press release.
Cautionary Note Regarding Forward-Looking Statements
This press release contains forward-looking statements within the meaning of The Private Securities Litigation Reform Act of 1995 including, but not limited to those statements regarding Schr dinger's expectations about the speed and capacity of its computational platform, its financial outlook for the fiscal year ending December 31, 2025 and third quarter ending September 30, 2025, its plans to continue to invest in research and its strategic plans to accelerate the growth of its software business and advance its collaborative and proprietary drug discovery programs, the long-term potential of its business, its ability to improve and advance the science underlying its platform, including its ability to improve drug discovery, the initiation, timing, progress, and results of its proprietary drug discovery programs and product candidates and the drug discovery programs and product candidates of its collaborators, the clinical potential and favorable properties of its MALT1, CDC7, Wee1 Myt1, and SOS1 inhibitors, including SGR-1505, SGR-2921, SGR-3515, and SGR-4174, the clinical potential and favorable properties of its collaborators' product candidates, the potential for SGR-1505 to be used for the treatment of relapsed refractory B-cell malignancies, including Waldenstr m macroglobulinemia and chronic lymphocytic leukemia, the potential benefits of Fast Track designation, including frequency of interactions with the FDA during clinical development and potentially accelerated approval and or priority review, its plans to explore strategic opportunities for the continued clinical development of SGR-1505, and Schr dinger's plans to engage with regulators, as well as expectations related to the use of its cash, cash equivalents and marketable securities. Statements including words such as "aim," "anticipate," "believe," "contemplate," "continue," "could," "estimate," "expect," "goal," "intend," "may," "might," "plan," "potential," "predict," "project," "should," "target," "will," "would" and statements in the future tense are forward-looking statements. These forward-looking statements reflect Schr dinger's current views about its plans, intentions, expectations, strategies and prospects, which are based on the information currently available to the company and on assumptions the company has made. Actual results may differ materially from those described in these forward-looking statements and are subject to a variety of assumptions, uncertainties, risks and important factors that are beyond Schr dinger's control, including the demand for its software platform, its ability to further develop its computational platform, its reliance upon third-party providers of cloud-based infrastructure to host its software solutions, factors adversely affecting the life sciences industry, fluctuations in the value of the U.S. dollar and foreign currencies, its reliance upon its third-party drug discovery collaborators, the uncertainties inherent in drug development and commercialization, such as the conduct of research activities and the timing of and its ability to initiate and complete preclinical studies and clinical trials, whether results from preclinical studies will be predictive of the results of later preclinical studies and clinical trials, uncertainties associated with the regulatory review of IND submissions, clinical trials and applications for marketing approvals, the ability to retain and hire key personnel and other risks detailed under the caption "Risk Factors" and elsewhere in the company's Securities and Exchange Commission filings and reports, including its Quarterly Report on Form 10-Q for the quarterly period ended June 30, 2025, filed with the Securities and Exchange Commission on August 6, 2025, as well as future filings and reports by the company. Any forward-looking statements contained in this
press release speak only as of the date hereof. Except as required by law, Schr dinger undertakes no duty or obligation to update any forward-looking statements contained in this press release as a result of new information, future events, changes in expectations or otherwise.
Matthew Luchini (Investors)
matthew.luchini schrodinger.com
Allie Nicodemo (Media)
allie.nicodemo schrodinger.com
Condensed Consolidated Statements of Operations (Unaudited)
(in thousands, except for share and per share amounts)
Three Months Ended June 30, Six Months Ended June 30,
2025 2024 2025 2024
Revenues
Software products and services $ 40,544 $ 35,404 $ 89,360 $ 68,819
Drug discovery 14,215 11,930 24,950 15,113
Total revenues 54,759 47,334 114,310 83,932
Cost of revenues
Software products and services 13,029 7,167 26,551 15,143
Drug discovery 15,572 8,832 30,477 18,564
Total cost of revenues 28,601 15,999 57,028 33,707
Gross profit 26,158 31,335 57,282 50,225
Operating expenses
Research and development 43,138 50,835 88,982 101,446
Sales and marketing 10,734 9,693 21,101 19,864
General and administrative 25,189 23,536 50,991 49,077
Total operating expenses 79,061 84,064 161,074 170,387
Loss from operations (52,903) (52,729) (103,792) (120,162)
Other income (expense)
Gain on equity investments - - - -
Change in fair value of equity investments 4,579 (5,833) (8,516) 2,304
Other income 5,438 4,598 9,642 9,626
Total other income (expense) 10,017 (1,235) 1,126 11,930
Loss before income taxes (42,886) (53,964) (102,666) (108,232)
Income tax expense 287 83 315 539
Net loss $ (43,173) $ (54,047) $ (102,981) $ (108,771)
Net loss per share of common and limited common stockholders, basic and diluted $ (0.59) $ (0.74) $ (1.41) $ (1.50)
Weighted average shares used to compute net loss per share of common and limited common stockholders, basic and diluted 73,427,635 72,711,685 73,243,797 72,501,409
Condensed Consolidated Balance Sheets (Unaudited)
(in thousands, except for share and per share amounts)
Assets June 30, 2025 December 31, 2024
Current assets
Cash and cash equivalents $ 219,901 $ 147,326
Restricted cash 12,079 15,331
Marketable securities 230,284 204,798
Accounts receivable, net of allowance for doubtful accounts of $350 and $210 10,073 235,692
Unbilled and other receivables, net of allowance for unbilled receivables of $140 and $100 26,711 19,641
Prepaid expenses 14,947 12,205
Total current assets 513,995 634,993
Property and equipment, net 21,709 24,196
Equity investments 34,691 43,208
Goodwill 4,791 4,791
Right of use assets - operating leases 107,346 111,883
Other assets 5,712 4,155
Total assets $ 688,244 $ 823,226
Liabilities and Stockholders' Equity
Current liabilities
Accounts payable 8,800 $ 10,666
Accrued payroll, taxes, and benefits 25,322 42,110
Deferred revenue 94,543 111,944
Lease liabilities - operating leases 16,841 16,755
Other accrued liabilities 10,263 10,272
Total current liabilities 155,769 191,747
Deferred revenue, long-term 91,995 108,814
Lease liabilities - operating leases, long-term 97,472 101,074
Other liabilities, long-term 136 146
Total liabilities 345,372 401,781
Stockholders' equity
Preferred stock, $0.01 par value. Authorized 10,000,000 shares zero shares issued and outstanding at June 30, 2025 and December 31, 2024, respectively - -
Common stock, $0.01 par value. Authorized 500,000,000 shares 64,420,899 and 63,710,409 shares issued and outstanding at June 30, 2025 and December 31, 2024 , respectively 644 637
Limited common stock, $0.01 par value. Authorized 100,000,000 shares 9,164,193 shares issued and outstanding at June 30, 2025 and December 31, 2024, respectively 92 92
Additional paid-in capital 970,687 946,037
Accumulated deficit (628,522) (525,541)
Accumulated other comprehensive (loss) income (29) 220
Total stockholders' equity 342,872 421,445
Total liabilities and stockholders' equity $ 688,244 $ 823,226
Condensed Consolidated Statements of Cash Flows (Unaudited)
Six Months Ended June 30,
2025 2024
Cash flows from operating activities
Net loss $ (102,981) $ (108,771)
Adjustments to reconcile net loss to net cash used in operating activities
Gain on equity investments - -
Fair value adjustments of equity investments 8,516 (2,304)
Depreciation and amortization 3,120 2,837
Stock-based compensation 22,201 25,026
Noncash investment accretion (1,676) (4,706)
Loss on disposal of property and equipment 20 7
Decrease (increase) in assets
Accounts receivable, net 225,619 54,143
Unbilled and other receivables (7,070) (17,197)
Reduction in the carrying amount of right of use assets - operating leases 4,537 4,205
Prepaid expenses and other assets (4,299) (6,118)
(Decrease) increase in liabilities
Accounts payable (1,737) (8,941)
Accrued payroll, taxes, and benefits (16,788) (7,443)
Deferred revenue (34,220) (17,395)
Lease liabilities - operating leases (3,516) (3,953)
Other accrued liabilities 139 (2,389)
Net cash provided by (used in) operating activities 91,865 (92,999)
Cash flows from investing activities
Purchases of property and equipment (910) (5,096)
Purchases of equity investments - (3,000)
Purchases of marketable securities (166,062) (153,513)
Proceeds from maturity of marketable securities 142,003 196,266
Net cash (used in) provided by investing activities (24,969) 34,657
Cash flows from financing activities
Proceeds from issuances of common stock upon stock option exercises 2,456 950
Principal payments on finance leases (29) (29)
Payment of offering costs - -
Proceeds from issuance of common stock in ATM offering - 8,691
Net cash provided by financing activities 2,427 9,612
Net increase (decrease) in cash and cash equivalents and restricted cash 69,323 (48,730)
Cash and cash equivalents and restricted cash, beginning of period 162,657 161,066
Cash and cash equivalents and restricted cash, end of period $ 231,980 $ 112,336
Supplemental disclosure of cash flow and noncash information
Cash paid for income taxes $ 365 $ 439
Supplemental disclosure of non-cash investing and financing activities
Purchases of property and equipment in accounts payable 34 435
Purchases of property and equipment in accrued liabilities - 331
Acquisition of right of use assets - operating leases, contingency resolution - 2,848
Reconciliation of GAAP to Non-GAAP Financial Measures (Unaudited)
Three Months Ended Six Months Ended
June 30, June 30,
2025 2024 2025 2024
(in thousands, except per share data)
Net loss (GAAP) $ (43,173) $ (54,047) $ (102,981) $ (108,771)
Income tax expense 287 83 315 539
Gain on equity investment - - - -
Change in fair value (4,579) 5,833 8,516 (2,304)
Non-GAAP net loss $ (47,465) $ (48,131) $ (94,150) $ (110,536)
Non-GAAP net loss per share of common and limited common stockholders, basic and diluted $ (0.65) $ (0.66) $ (1.29) $ (1.52)
Weighted average shares used to compute non-GAAP net loss per share of common and limited common stockholders, basic and diluted 73,427,635 72,711,685 73,243,797 72,501,409
Last updated: Aug 6, 2025