Coherus Oncology Reports Third Quarter 2025 Financial Results and Provides Business Update
Coherus Oncology (NASDAQ: CHRS) reported Q3 2025 results and a business update on Nov 6, 2025. LOQTORZI net revenue was $11.2M in Q3, up 12% QoQ and 92% YoY; total net revenue from continuing operations was $11.6M for the quarter. Cash, cash equivalents and marketable securities were $191.7M as of Sept 30, 2025. R&D spending rose to $27.3M in Q3 while SG&A declined to $24.9M. Net loss from continuing operations was $44.5M, or $(0.38) per share, with non-GAAP net loss of $38.9M. Pipeline progress includes expansion of CHS-114 into colorectal cancer and multiple 2026 readouts for CHS-114 and casdozokitug.
Coherus Oncology (NASDAQ: CHRS) ha riportato i risultati del terzo trimestre 2025 e un aggiornamento sull’andamento dell’azienda il 6 novembre 2025. LOQTORZI ricavi netti sono stati di 11,2 milioni di dollari nel terzo trimestre, +12% QoQ e +92% YoY; i ricavi netti totali dalle operazioni in corso sono stati di 11,6 milioni di dollari per il trimestre. Cash, cash equivalents and marketable securities erano di 191,7 milioni di dollari al 30 settembre 2025. Le spese di R&D sono aumentate a 27,3 milioni di dollari nel terzo trimestre, mentre SG&A è diminuita a 24,9 milioni. La perdita netta dalle operazioni in corso è stata di 44,5 milioni di dollari, o (0,38) dollari per azione, con una perdita netta non-GAAP di 38,9 milioni. Il progresso del pipeline include l’espansione di CHS-114 nel cancro colorettale e molte letture previste per il 2026 per CHS-114 e casdozokitug.
Coherus Oncology (NASDAQ: CHRS) informó los resultados del tercer trimestre de 2025 y una actualización comercial el 6 de noviembre de 2025. LOS ingresos netos de LOQTORZI fueron de 11,2 millones de dólares en el tercer trimestre, un aumento del 12% trimestre a trimestre y del 92% año tras año; los ingresos netos totales de las operaciones continuas fueron de 11,6 millones de dólares para el trimestre. Efectivo, equivalentes de efectivo y valores negociables eran de 191,7 millones de dólares a 30 de septiembre de 2025. El gasto en I+D aumentó a 27,3 millones de dólares en el tercer trimestre, mientras que SG&A descendió a 24,9 millones. La pérdida neta de las operaciones continuas fue de 44,5 millones de dólares, o (0,38) por acción, con una pérdida neta no GAAP de 38,9 millones. El progreso de la cartera incluye la expansión de CHS-114 al cáncer colorrectal y múltiples anuncios de 2026 para CHS-114 y casdozokitug.
Coherus Oncology (NASDAQ: CHRS)는 2025년 11월 6일에 2025년 3분기 실적 발표 및 기업 업데이트를 발표했습니다. LOQTORZI 순매출은 3분기에 1120만 달러로 QoQ 12% 증가, YoY 92% 증가; 계속사업의 총 순매출은 분기에 1160만 달러였습니다. 현금, 현금성자산 및 시가가능증권은 2025년 9월 30일 기준으로 1억 9170만 달러였습니다. 연구개발(R&D) 지출은 3분기에 2730만 달러로 증가했고 SG&A는 2490만 달러로 감소했습니다. 계속사업의 순손실은 4450만 달러로 주당 0.38달러의 손실이었고, 비GAAP 순손실은 3890만 달러였습니다. 파이프라인 진행에는 CHS-114의 대장암 확장 및 CHS-114와 casdozokitug의 2026년 다수 공시가 포함됩니다.
Coherus Oncology (NASDAQ: CHRS) a publié les résultats du T3 2025 et une mise à jour de l’activité le 6 novembre 2025. les revenus nets de LOQTORZI s’élevèrent à 11,2 M$ au T3, en hausse de 12% QoQ et de 92% YoY; les revenus nets totaux des opérations poursuivies furent de 11,6 M$ pour le trimestre. Liquidités, équivalents de liquidités et titres négociables s’élevaient à 191,7 M$ au 30 septembre 2025. Les dépenses de R&D ont augmenté pour atteindre 27,3 M$ au T3 tandis que les SG&A ont diminué à 24,9 M$. La perte nette des opérations continues s’élevait à 44,5 M$, soit (0,38) $ par action, avec une perte nette non GAAP de 38,9 M$. Les progrès du pipeline incluent l’expansion de CHS-114 dans le cancer colorectal et plusieurs lectures prévues pour 2026 pour CHS-114 et casdozokitug.
Coherus Oncology (NASDAQ: CHRS) berichtete am 6. November 2025 über die Ergebnisse des dritten Quartals 2025 und ein Update zum Geschäft. LOQTORZI Nettoumsatz betrug im dritten Quartal 11,2 Mio. USD, QoQ +12% und YoY +92%; der Gesamt-Nettoumsatz aus fortgeführten Geschäftsfeldern betrug 11,6 Mio. USD für das Quartal. Cash, Zahlungsmitteläquivalente und marktfähige Wertpapiere beliefen sich zum 30. September 2025 auf 191,7 Mio. USD. Die F&E-Ausgaben stiegen im Q3 auf 27,3 Mio. USD, während SG&A auf 24,9 Mio. USD sanken. Die Nettolosstrata aus fortgeführten Geschäftsfeldern betrug 44,5 Mio. USD, oder 0,38 USD je Aktie, mit einer nicht-GAAP Nettoloss von 38,9 Mio. USD. Die Pipeline-Entwicklung umfasst die Ausweitung von CHS-114 in Darmkrebs und mehrere 2026-Lesungen für CHS-114 und casdozokitug.
كونيروس أونكولوجي (ناسداك: CHRS) أصدرت نتائج الربع الثالث من 2025 وتحديثًا للأعمال في 6 نوفمبر 2025. إيرادات LOQTORZI الصافية كانت 11.2 مليون دولار في الربع الثالث، بارتفاع 12% فصليًا و92% سنويًا؛ الإجمالي من العمليات المستمرة كان 11.6 مليون دولار لهذا الربع. النقد وما يعادله من النقد والأوراق المالية القابلة للتداول كان 191.7 مليون دولار حتى 30 سبتمبر 2025. ارتفع الإنفاق على البحث والتطوير إلى 27.3 مليون دولار في الربع الثالث بينما انخفض SG&A إلى 24.9 مليون دولار. الخسارة الصافية من العمليات المستمرة بلغت 44.5 مليون دولار، أو 0.38 دولار للسهم، مع خسارة صافية غير GAAP قدرها 38.9 مليون دولار. يتضمن تقدم خط الأنابيب توسع CHS-114 في سرطان القولون والمستقيم والعديد من قراءات 2026 لـ CHS-114 وcasdozokitug.
- LOQTORZI revenue +92% YoY
- LOQTORZI QoQ growth +12% (Q3 2025 vs Q2 2025)
- Cash balance $191.7M at 9/30/2025
- Pipeline readouts multiple initial data readouts expected in 2026
- Q3 net loss $44.5M (continuing operations)
- R&D spend increased to $27.3M in Q3
- Accrued obligations $67.0M largely UDENYCA-related on balance sheet
Insights
Mixed commercial traction and stronger liquidity offset by continued R&D spend and quarterly losses; key clinical readouts in 2026 will drive material value catalysts.
LOQTORZI shows commercial momentum with net product revenue of
Pipeline progress centers on CHS-114 (CCR8 Treg depleter) expansion into colorectal cancer and multiple ongoing combination studies; casdozokitug biomarker and combination signals were presented and support continued development. However, the company recorded a GAAP net loss of
Principal dependencies and risks include enrollment and readout quality for the CHS-114 and casdozokitug programs, the pace of LOQTORZI adoption outside specialist centers despite NCCN preferred status, and settlement timing for accrued obligations tied to the UDENYCA divestiture. Recent one-time charges (intangible write-offs and CVR adjustments) modestly affect comparability of SG&A trends.
Watch items and timing: SITC presentation on
– CHS-114, a highly selective Treg depleter, clinical program expanded to include colorectal cancer –
– Q3 2025 ending cash, cash equivalents and marketable securities of
– LOQTORZI® net revenue was
– Conference call today at 5:00 p.m. Eastern Standard Time –
REDWOOD CITY, Calif., Nov. 06, 2025 (GLOBE NEWSWIRE) -- Coherus Oncology, Inc. (Nasdaq: CHRS), today reported financial results for the third quarter ended September 30, 2025 and provided an overview of recent business highlights.
“In Q3 2025, we gained significant momentum on our strategy to develop innovative oncology therapies that substantially increase patient survival,” said Denny Lanfear, Coherus Chairman and Chief Executive Officer. “The vast majority of our study sites are enrolling, driving towards multiple data readouts in 2026 across a number of tumor types. We have now expanded our CHS-114 CCR8 Treg depleter clinical program to include colorectal cancer, an area of growing unmet need, impacting even younger patients.”
“The importance of CCR8 as a cancer target is highlighted by the 2025 Nobel Prize in Physiology or Medicine, which recognized the pivotal role of Treg cells in peripheral immune tolerance and their pathological role in autoimmunity and cancer,” said Theresa LaVallee, PhD, Coherus Chief Scientific and Development Officer. Coherus Oncology was recently honored to present our clinical data on CHS-114 showing the cytolytic antibody’s potency and selectively, with robust tumoral Treg depletion, immune activation and a good safety profile at a SITC presentation focused on a deep dive into development of antibodies targeting CCR8 Tregs, reflecting our scientific leadership in this rapidly evolving field.”
“Our clinical programs target tumor types where there is a clear biological rationale and a significant unmet medical need with available therapies,” said Rosh Dias, MD, Chief Medical Officer. “We have previously shown encouraging data for both casdozokitug and CHS-114, and we expect maturing datasets from our ongoing studies throughout 2026.”
RECENT BUSINESS HIGHLIGHTS
LOQTORZI® (toripalimab-tpzi) Commercial Updates
- LOQTORZI remains the only FDA-approved and available treatment in the U.S. for recurrent, locally advanced or metastatic nasopharyngeal carcinoma (NPC), in all patient subsets and across all lines of therapy.
- LOQTORZI net revenue for Q3 2025 was
$11.2 million , a12% increase over$10.0 million in Q2 2025 and a92% increase over LOQTORZI net revenue of$5.8 million in Q3 2024. Growth in Q3 2025 was driven largely by higher patient demand from both increasing new account starts as well as repeat use in existing accounts. Average duration of treatment among existing patients also continues to grow. - Increasing awareness of the revised National Comprehensive Cancer Network (NCCN) guidelines granting LOQTORZI preferred status within the NPC indication continues to drive strong demand growth among head & neck cancer specialists. The Company’s focus remains on deepening adoption within general oncologists in the community setting by driving education on clinical data and updated NCCN guidelines. While half of all NPC patients in the U.S. are managed in this setting, market penetration will continue at a steady and gradual pace due to the rarity of patients seen by these oncologists.
ADVANCEMENT OF INNOVATIVE, NEXT-GENERATION ONCOLOGY PIPELINE
LOQTORZI is a next-generation PD-1 marketed in the U.S. in two indications.
- Coherus plans to maximize the value of this medicine by combining LOQTORZI with internal pipeline candidates, CHS-114 and casdozokitug, for additional solid tumor indications and entering into capital-efficient external partnerships for label expansions.
- In October 2025, the Cancer Research Institute announced the first patient enrolled in the third cohort of the ongoing Immunotherapy Platform Study in Platinum-Resistant High-Grade Serous Ovarian Cancer (IPROC) (NCT04918186). The third cohort of the Phase 2 trial is evaluating LOQTORZI in combination with ENB Therapeutics' ENB-003 for the treatment of ovarian cancer.
CHS-114 is a highly selective cytolytic CCR8 antibody that specifically binds and preferentially depletes CCR8+ tumor regulatory T cells (Tregs) with no off-target binding.
- Updated biomarker data from the Phase 1b study dose expansion study in 2L+ head and neck squamous cell carcinoma (HNSCC) will be presented on Saturday, November 8, 2025 at the 40th Annual Meeting of the Society for Immunotherapy of Cancer (SITC).
- Phase 1b CHS-114/toripalimab combination dose optimization studies in 2L HNSCC and 2L gastric cancers are underway, with initial data readouts for HNSCC expected in 1H 2026.
- A Phase 1b study evaluating the CHS-114/toripalimab combination, with and without chemotherapy, in 1L and 2L esophageal squamous cell carcinoma (ESCC), respectively, is underway with a first data readout expected in mid-2026.
- A Phase 1b/2a study evaluating CHS-114/toripalimab combination in 4L+ colorectal cancer is enrolling patients and initial data is expected in 2H 2026.
Casdozokitug is a first-in-class, clinical-stage IL-27 antagonist, with demonstrated monotherapy activity in treatment-refractory non-small cell lung cancer (NSCLC) and clear cell renal cell carcinoma (ccRCC) and combination activity in hepatocellular carcinoma (HCC).
- Enrollment is ongoing in the Phase 2 randomized trial of casdozokitug/toripalimab/bevacizumab in 1L HCC, with the first data readout expected in mid-2026.
- On November 2, 2025, new data was presented at the Cytokines 2025 annual meeting demonstrating casdozokitug promotes NK and T cell activity, and antitumor response in patients with advanced solid tumors. These biomarker data continue to support treatment with casdozokitug which leads to inhibition of IL-27 signaling and enhanced cytolytic immune activity (by NK and T cells). The new data reveal these biomarker changes following treatment of HCC patients with casdozokitug and standard of care are associated with clinical response (and thus, support an important contribution of casdozokitug).
THIRD QUARTER 2025 FINANCIAL RESULTS
Net revenue from continuing operations was
Cost of goods sold (COGS) from continuing operations was
Research and development (R&D) expenses from continuing operations were
Selling, general and administrative (SG&A) expenses from continuing operations were
Interest expense from continuing operations was
Net loss from continuing operations for the third quarter of 2025 was
Non-GAAP net loss from continuing operations for the third quarter of 2025 was
Cash, cash equivalents and marketable securities totaled
Conference Call Information
When: Thursday, November 6, 2025, starting at 5:00 p.m. Eastern Standard Time
To access the conference call, please pre-register through the following link to receive dial-in information and a personal PIN to access the live call: https://register-conf.media-server.com/register/BI8cec893e4a1a4d98a4596ef8068cb4bd
Webcast: https://edge.media-server.com/mmc/p/d2g4jyb4
A live and archived webcast will be available on the “Investors” section of the Coherus website at https://investors.coherus.com/events-presentations.
Please dial in 15 minutes early to ensure a timely connection to the call.
About Coherus Oncology
Coherus Oncology is a fully integrated commercial-stage innovative oncology company with an approved next-generation PD-1 inhibitor, LOQTORZI® (toripalimab-tpzi), and a pipeline that includes two mid-stage clinical candidates targeting liver, lung, head & neck, colorectal and other cancers. The Company’s strategy is to grow sales of LOQTORZI in NPC and advance the development of new indications for LOQTORZI in combination with both its pipeline candidates as well as through its partners, driving sales multiples and synergies from proprietary combinations.
Coherus’ innovative oncology pipeline includes multiple antibody immunotherapy candidates focused on enhancing the innate and adaptive immune responses to enable a robust antitumor response and enhance outcomes for patients with cancer. CHS-114 is a highly selective cytolytic anti-CCR8 antibody currently in Phase 1b/2a studies in patients with advanced solid tumors, including head and neck squamous cell carcinoma, colorectal cancer, gastric cancer, and esophageal cancer. Casdozokitug is a novel IL-27 antagonistic antibody currently being evaluated in a Phase 2 study in patients with first-line hepatocellular carcinoma.
For more information about LOQTORZI, including the U.S. Prescribing Information and important safety information, please visit www.loqtorzi.com.
Forward-Looking Statements
Except for the historical information contained herein, the matters set forth in this press release are forward-looking statements within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995, Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. Forward-looking statements contained in this press release may be identified by the use of words such as “may,” “will,” “should,” “expect,” “plan,” “anticipate,” “could,” “intend,” “target,” “project,” “contemplate,” “believe,” “estimate,” “predict,” “potential” or “continue” or the negative of these terms or other similar expressions. These statements are based on the Company's current beliefs and expectations. Such forward looking statements include, but are not limited to, statements regarding Coherus’ expectations about identifying sales multiples and synergies; the ability of Coherus’ I-O pipeline to enhance outcomes for cancer patients; projections for cash runway; the ability to reduce risk for Coherus’ pipeline; expectations for the timing when Coherus will be able to commence future clinical studies or receive clinical data for its product candidates; Coherus’ ability to enter into additional partnerships; Coherus’ ability to grow revenues; and Coherus’ expectations about total addressable opportunity for each of its product candidates.
Such forward-looking statements involve substantial risks and uncertainties that could cause Coherus’ actual results, performance or achievements to differ significantly from any future results, performance or achievements expressed or implied by the forward-looking statements. Such risks and uncertainties include, among others, the risks and uncertainties inherent in the clinical drug development process; risks related to Coherus’ dependence on an ability to raise funds in the future, which may not be available on acceptable terms or at all; risks related to Coherus’ existing and potential collaboration partners; risks of Coherus’ competitive position; the risks and uncertainties of the regulatory approval process, including the speed of regulatory review and the timing of Coherus’ regulatory filings; the risk of FDA review issues; and the risks and uncertainties of possible litigation. All forward-looking statements contained in this press release speak only as of the date of this press release. Coherus undertakes no obligation to update or revise any forward-looking statements. For a further description of the significant risks and uncertainties that could cause actual results to differ from those expressed in these forward-looking statements, as well as risks relating to Coherus’ business in general, see Coherus’ quarterly report on Form 10-Q for the fiscal quarter ended September 30, 2025 filed with the Securities and Exchange Commission on or about the date of this press release, including the section therein captioned “Risk Factors” and in other documents Coherus files with the Securities and Exchange Commission. Coherus’ results for the fiscal quarter ended September 30, 2025 are not necessarily indicative of its operating results for any future periods.
LOQTORZI®, whether or not appearing in large print or with the trademark symbol, is a registered trademark of Coherus Oncology, Inc.
©2025 Coherus Oncology, Inc. All rights reserved.
Coherus Contact Information:
For Investors & Media:
Carrie Graham
Vice President, Investor Relations and Advocacy
IR@coherus.com
| Coherus Oncology, Inc. Condensed Consolidated Statements of Operations (in thousands, except share and per share data) (unaudited) | ||||||||||||||||
| Three Months Ended | Nine Months Ended | |||||||||||||||
| September 30, | September 30, | |||||||||||||||
| 2025 | 2024 | 2025 | 2024 | |||||||||||||
| Net revenue | $ | 11,571 | $ | 6,052 | $ | 29,424 | $ | 18,656 | ||||||||
| Costs and expenses: | ||||||||||||||||
| Cost of goods sold | 3,721 | 2,729 | 9,769 | 5,977 | ||||||||||||
| Research and development | 27,252 | 22,052 | 77,914 | 71,074 | ||||||||||||
| Selling, general and administrative | 24,931 | 28,127 | 76,995 | 95,874 | ||||||||||||
| Total costs and expenses | 55,904 | 52,908 | 164,678 | 172,925 | ||||||||||||
| Loss from operations | (44,333 | ) | (46,856 | ) | (135,254 | ) | (154,269 | ) | ||||||||
| Interest expense | (2,325 | ) | (2,827 | ) | (6,752 | ) | (8,822 | ) | ||||||||
| Loss on debt extinguishment | — | — | — | (12,630 | ) | |||||||||||
| Other income (expense), net | 2,141 | 2,084 | 5,229 | 6,420 | ||||||||||||
| Loss from continuing operations before income taxes | (44,517 | ) | (47,599 | ) | (136,777 | ) | (169,301 | ) | ||||||||
| Income tax provision | — | — | — | — | ||||||||||||
| Net loss from continuing operations | (44,517 | ) | (47,599 | ) | (136,777 | ) | (169,301 | ) | ||||||||
| Net income from discontinued operations, net of tax | 8,986 | 36,848 | 342,444 | 248,504 | ||||||||||||
| Net income (loss) | $ | (35,531 | ) | $ | (10,751 | ) | $ | 205,667 | $ | 79,203 | ||||||
| Net income (loss) per share: | ||||||||||||||||
| Net loss from continuing operations - basic and diluted | $ | (0.38 | ) | $ | (0.41 | ) | $ | (1.18 | ) | $ | (1.48 | ) | ||||
| Net income from discontinued operations - basic and diluted | $ | 0.08 | $ | 0.32 | $ | 2.95 | $ | 2.17 | ||||||||
| Net income (loss) per share - basic and diluted | $ | (0.31 | ) | $ | (0.09 | ) | $ | 1.77 | $ | 0.69 | ||||||
| Weighted-average number of shares used in computing net income (loss) per share: | ||||||||||||||||
| Basic and diluted | 116,229,170 | 115,210,091 | 116,056,247 | 114,263,256 | ||||||||||||
| Coherus Oncology, Inc. Condensed Consolidated Balance Sheets (in thousands) (unaudited) | |||||||
| September 30, | December 31, | ||||||
| 2025 | 2024 | ||||||
| Assets | |||||||
| Cash and cash equivalents | $ | 103,352 | $ | 125,987 | |||
| Investments in marketable securities | 88,311 | — | |||||
| Trade receivables, net | 9,245 | 111,324 | |||||
| TSA receivables, net | 241,251 | 11,010 | |||||
| Inventory | 2,048 | 4,207 | |||||
| Intangible assets, net | 49,484 | 53,646 | |||||
| Other assets | 22,828 | 25,936 | |||||
| Assets of discontinued operations | — | 116,423 | |||||
| Total assets | $ | 516,519 | $ | 448,533 | |||
| Liabilities and Stockholders’ Equity (Deficit) | |||||||
| Accrued rebates, fees and reserve | $ | 67,010 | $ | 164,867 | |||
| TSA payables and other accrued liabilities | 253,908 | 11,026 | |||||
| Term loan | 36,957 | 36,698 | |||||
| Convertible notes | 121 | 228,229 | |||||
| Other liabilities | 70,749 | 139,703 | |||||
| Total stockholders' equity (deficit) | 87,774 | (131,990 | ) | ||||
| Total liabilities and stockholders’ equity (deficit) | $ | 516,519 | $ | 448,533 | |||
| Coherus Oncology, Inc. Condensed Consolidated Statements of Cash Flows (in thousands) (unaudited) | ||||||||||||||||
| Three Months Ended | Nine Months Ended | |||||||||||||||
| September 30, | September 30, | |||||||||||||||
| 2025 | 2024 | 2025 | 2024 | |||||||||||||
| Cash, cash equivalents and restricted cash at beginning of the period | $ | 217,156 | $ | 159,692 | $ | 126,250 | $ | 103,343 | ||||||||
| Net cash used in operating activities | (46,339 | ) | (62,016 | ) | (118,797 | ) | (49,048 | ) | ||||||||
| Purchases of investments in marketable securities | (68,850 | ) | — | (89,576 | ) | — | ||||||||||
| Proceeds from maturities of investments in marketable securities | 1,650 | — | 1,650 | 6,200 | ||||||||||||
| Proceeds from sale of investments in marketable securities | — | — | — | 8,688 | ||||||||||||
| Net cash received related to the Sale Transactions | — | — | 478,681 | 227,823 | ||||||||||||
| Milestone payment to Junshi Biosciences | — | — | (12,500 | ) | (12,500 | ) | ||||||||||
| Other investing activities, net | (27 | ) | 444 | (330 | ) | 652 | ||||||||||
| Net cash (used in) provided by investing activities | (67,227 | ) | 444 | 377,925 | 230,863 | |||||||||||
| Proceeds from 2029 Term loan, net of debt discount & issuance costs | — | (141 | ) | — | 36,979 | |||||||||||
| Proceeds from (repayment of) Revenue Purchase and Sale Agreement, net of issuance costs | — | (9 | ) | (47,652 | ) | 36,486 | ||||||||||
| Proceeds from issuance of common stock under ATM Offering, net of issuance costs | — | — | — | 1,455 | ||||||||||||
| Proceeds from purchase under the employee stock purchase plan | — | — | 188 | 685 | ||||||||||||
| Taxes paid related to net share settlement | (3 | ) | (10 | ) | (283 | ) | (2,466 | ) | ||||||||
| Redemption of 2026 Convertible Notes, including transaction costs | — | — | (233,185 | ) | — | |||||||||||
| Repayment of 2027 Term Loans, premiums and fees | — | — | — | (260,387 | ) | |||||||||||
| Other financing activities, net | 5 | (7 | ) | (854 | ) | 43 | ||||||||||
| Net cash provided by (used in) financing activities | 2 | (167 | ) | (281,786 | ) | (187,205 | ) | |||||||||
| Net decrease in cash, cash equivalents and restricted cash | (113,564 | ) | (61,739 | ) | (22,658 | ) | (5,390 | ) | ||||||||
| Cash, cash equivalents and restricted cash at end of the period | $ | 103,592 | $ | 97,953 | $ | 103,592 | $ | 97,953 | ||||||||
Non-GAAP Financial Measures
To supplement the financial results presented in accordance with GAAP, Coherus has also included in this press release non-GAAP net loss from continuing operations, and the related per share measures, which exclude from net loss from continuing operations and the related per share measures, stock-based compensation expense, amortization and impairments of intangible assets, loss on debt extinguishment, and change in fair value of our Royalty Fee Derivative Liability. These non-GAAP financial measures are not prepared in accordance with GAAP, do not serve as an alternative to GAAP and may be calculated differently than similar non-GAAP financial information disclosed by other companies. Coherus encourages investors to carefully consider its results under GAAP, as well as its supplemental non-GAAP financial information and the reconciliation between these presentations set forth below, to more fully understand Coherus’ business.
Coherus believes that the presentation of these non-GAAP financial measures provides useful supplemental information to, and facilitates additional analysis by, investors. In particular, Coherus believes that these non-GAAP financial measures, when considered together with its financial information prepared in accordance with GAAP, can enhance investors’ and analysts’ ability to meaningfully compare Coherus’ results from period to period, and to identify operating trends in Coherus’ business. Coherus also regularly uses these non-GAAP financial measures internally to understand, manage and evaluate its business and to make operating decisions.
| Coherus Oncology, Inc. Reconciliation of GAAP Net Loss from Continuing Operations to Non-GAAP Net Loss from Continuing Operations (in thousands, except share and per share data) (unaudited) | ||||||||||||||||
| Three Months Ended | Nine Months Ended | |||||||||||||||
| September 30, | September 30, | |||||||||||||||
| 2025 | 2024 | 2025 | 2024 | |||||||||||||
| GAAP net loss from continuing operations | $ | (44,517 | ) | $ | (47,599 | ) | $ | (136,777 | ) | $ | (169,301 | ) | ||||
| Adjustments: | ||||||||||||||||
| Stock-based compensation expense | 3,322 | 6,438 | 13,535 | 20,113 | ||||||||||||
| Loss on debt extinguishment | — | — | — | 12,630 | ||||||||||||
| Impairment of out-license asset and remeasurement of CVR liability, net | 1,646 | — | 1,646 | 6,772 | ||||||||||||
| Change in fair value of Royalty Fee Derivative Liability | — | — | 810 | — | ||||||||||||
| Amortization of intangible assets | 652 | 1,142 | 1,986 | 2,684 | ||||||||||||
| Non-GAAP net loss from continuing operations | $ | (38,897 | ) | $ | (40,019 | ) | $ | (118,800 | ) | $ | (127,102 | ) | ||||
| GAAP | ||||||||||||||||
| Net loss per share from continuing operations, basic and diluted | $ | (0.38 | ) | $ | (0.41 | ) | $ | (1.18 | ) | $ | (1.48 | ) | ||||
| Shares used in computing basic and diluted net loss per share | 116,229,170 | 115,210,091 | 116,056,247 | 114,263,256 | ||||||||||||
| Non-GAAP | ||||||||||||||||
| Net loss per share from continuing operations, basic and diluted | $ | (0.33 | ) | $ | (0.35 | ) | $ | (1.02 | ) | $ | (1.11 | ) | ||||
| Shares used in computing basic and diluted net loss per share | 116,229,170 | 115,210,091 | 116,056,247 | 114,263,256 | ||||||||||||