I-Mab Reports Second Quarter 2025 Financial Results and Provides Business Update
I-Mab (NASDAQ: IMAB) reported Q2 2025 financial results and business updates, highlighting significant progress in its oncology pipeline. The company's lead drug givastomig showed promising Phase 1b results with an 83% objective response rate in combination with immunochemotherapy for first-line gastric cancers.
I-Mab strengthened its financial position through an underwritten offering raising $61.2 million, resulting in a pro-forma cash balance of $226.8 million as of June 30, 2025. This funding is expected to sustain operations through Q4 2028. The company reported reduced R&D expenses of $3.3 million for Q2 2025, down from $5.2 million in Q2 2024, and a net loss of $5.5 million for Q2 2025.
Key upcoming milestones include topline data from givastomig's Phase 1b dose expansion study expected in Q1 2026. The company also acquired Bridge Health, strengthening its intellectual property portfolio for givastomig.
I-Mab (NASDAQ: IMAB) ha annunciato i risultati finanziari del secondo trimestre 2025 e aggiornamenti aziendali, mettendo in evidenza notevoli progressi nel suo portafoglio oncologico. Il farmaco di punta givastomig ha mostrato risultati promettenti nella Fase 1b con un tasso di risposta oggettiva dell'83% in combinazione con immunochemioterapia nel trattamento di prima linea dei tumori gastrici.
I-Mab ha rafforzato la propria posizione finanziaria tramite un'offerta sottoscritta che ha raccolto 61,2 milioni di dollari, portando a un saldo di cassa pro-forma di 226,8 milioni di dollari al 30 giugno 2025. Questo finanziamento dovrebbe sostenere le operazioni fino al quarto trimestre del 2028. L'azienda ha registrato una riduzione delle spese di R&S a 3,3 milioni di dollari nel Q2 2025, rispetto a 5,2 milioni nel Q2 2024, e una perdita netta di 5,5 milioni di dollari per il Q2 2025.
I principali traguardi imminenti includono i dati topline dello studio di espansione della dose in Fase 1b di givastomig, attesi nel Q1 2026. L'azienda ha inoltre acquisito Bridge Health, rafforzando il proprio portafoglio di proprietà intellettuale relativo a givastomig.
I-Mab (NASDAQ: IMAB) informó los resultados financieros del segundo trimestre de 2025 y actualizaciones comerciales, destacando importantes avances en su cartera oncológica. El fármaco principal givastomig mostró resultados prometedores en la Fase 1b con una tasa de respuesta objetiva del 83% en combinación con inmunoquimioterapia para cánceres gástricos de primera línea.
I-Mab fortaleció su posición financiera mediante una oferta suscrita que recaudó 61,2 millones de dólares, resultando en un saldo de efectivo pro forma de 226,8 millones de dólares al 30 de junio de 2025. Se espera que estos fondos sostengan las operaciones hasta el cuarto trimestre de 2028. La compañía reportó una reducción en gastos de I+D a 3,3 millones de dólares en el Q2 2025, frente a 5,2 millones en el Q2 2024, y una pérdida neta de 5,5 millones de dólares en el Q2 2025.
Los hitos clave incluyen los datos principales del estudio de expansión de dosis de Fase 1b de givastomig, previstos para el Q1 2026. La compañía también adquirió Bridge Health, fortaleciendo su cartera de propiedad intelectual para givastomig.
I-Mab (NASDAQ: IMAB)은 2025년 2분기 실적 및 사업 현황을 발표하며 항암제 파이프라인에서의 상당한 진전을 강조했습니다. 주력 약물 기바스토미그(givastomig)은 일차 위암에 대한 면역화학요법 병용요법에서 객관적 반응률 83%라는 유망한 1b상 결과를 보였습니다.
I-Mab은 6120만 달러 규모의 인수인수형(언더라이터) 공모를 통해 재무구조를 강화했고, 그 결과 2025년 6월 30일 기준 프로포르마 현금 잔액 2억2680만 달러를 확보했습니다. 이 자금은 2028년 4분기까지 운영을 지원할 것으로 예상됩니다. 회사는 연구개발비를 2025년 2분기 330만 달러로 줄였으며(2024년 2분기 520만 달러에서 감소), 2025년 2분기 순손실은 550만 달러였습니다.
향후 주요 마일스톤으로는 기바스토미그 1b상 용량 확장 연구의 톱라인 데이터가 2026년 1분기에 발표될 예정입니다. 또한 회사는 Bridge Health를 인수해 기바스토미그의 지적재산 포트폴리오를 강화했습니다.
I-Mab (NASDAQ: IMAB) a publié ses résultats financiers du deuxième trimestre 2025 et des mises à jour opérationnelles, soulignant des progrès significatifs dans son portefeuille oncologique. Le médicament phare givastomig a montré des résultats prometteurs en Phase 1b avec un taux de réponse objective de 83% en combinaison avec une immunochimiothérapie pour les cancers gastriques de première ligne.
I-Mab a renforcé sa position financière via une offre garantie ayant levé 61,2 millions de dollars, aboutissant à un solde de trésorerie pro forma de 226,8 millions de dollars au 30 juin 2025. Ce financement devrait permettre de couvrir les opérations jusqu'au quatrième trimestre 2028. La société a déclaré une baisse des dépenses de R&D à 3,3 millions de dollars pour le T2 2025, contre 5,2 millions au T2 2024, et une perte nette de 5,5 millions de dollars pour le T2 2025.
Les jalons à venir incluent les données topline de l'étude d'expansion de dose de Phase 1b de givastomig, attendues au T1 2026. L'entreprise a également acquis Bridge Health, renforçant son portefeuille de propriété intellectuelle lié à givastomig.
I-Mab (NASDAQ: IMAB) berichtete über die Finanzergebnisse und Geschäftsneuigkeiten für das zweite Quartal 2025 und hob dabei erhebliche Fortschritte im Onkologie-Portfolio hervor. Das führende Medikament givastomig zeigte vielversprechende Phase‑1b‑Ergebnisse mit einer objektiven Ansprechrate von 83% in Kombination mit Immunchemotherapie bei Erstlinien-Magenkrebs.
I-Mab stärkte seine finanzielle Lage durch ein gezeichnetes Angebot, das 61,2 Millionen US‑Dollar einbrachte, was zu einem pro‑forma‑Kassenbestand von 226,8 Millionen US‑Dollar zum 30. Juni 2025 führte. Diese Mittel sollen den Betrieb voraussichtlich bis zum vierten Quartal 2028 finanzieren. Die Gesellschaft meldete verringerte F&E‑Aufwendungen in Höhe von 3,3 Millionen US‑Dollar im Q2 2025 (gegenüber 5,2 Millionen im Q2 2024) und einen Nettoverlust von 5,5 Millionen US‑Dollar im Q2 2025.
Wichtige bevorstehende Meilensteine sind die Topline‑Daten der Dosisexpansionsstudie von givastomig in Phase 1b, die für Q1 2026 erwartet werden. Zudem erwarb das Unternehmen Bridge Health und stärkte damit das geistige Eigentum rund um givastomig.
- None.
- Net loss of $5.5 million in Q2 2025
- Decreased interest income due to lower cash balances and market rates
- Dilution from new share offering increasing outstanding shares by 41%
Insights
I-Mab reports promising givastomig data in gastric cancer with 83% response rate while extending cash runway to Q4 2028 through $61.2M offering.
I-Mab's second quarter results highlight significant advancement of their lead asset givastomig, a CLDN18.2 x 4-1BB bispecific antibody targeting gastric cancer. The 83% objective response rate observed in the Phase 1b dose escalation study when combined with immunochemotherapy is particularly impressive compared to typical response rates in this indication. These responses were characterized as rapid, durable, and deepening over time – all critical factors for clinical meaningfulness.
On the financial front, I-Mab has substantially strengthened its position through a
The company has demonstrated improved operational efficiency with R&D expenses declining to
The company's strategic acquisition of Bridge Health eliminates royalty obligations and reduces future milestone payments for givastomig, strengthening their intellectual property position and potentially improving the economics of their lead program. With topline data from the givastomig Phase 1b expansion cohort expected in Q1 2026, I-Mab has positioned itself as a focused clinical-stage biotech with sufficient capital to reach meaningful data readouts.
- Positive givastomig Phase 1b dose escalation data in combination with immunochemotherapy in patients with 1L gastric cancers presented at ESMO GI 2025 showing
83% ORR at doses selected for ongoing expansion study - Topline data from planned dose expansion study of givastomig expected in Q1 2026
- Strengthened balance sheet with net proceeds of approximately
$61.2 million from August 2025 underwritten offering; pro-forma cash balance of approximately$226.8 million as of June 30, 2025, after giving effect to the offering; expected to fund planned operating expenses and capital expenditures through the fourth quarter of 2028
ROCKVILLE, Md., Aug. 20, 2025 (GLOBE NEWSWIRE) -- I-Mab (NASDAQ: IMAB) (I-Mab or the Company), a U.S.-based, global biotech company, focused on the development of precision immuno-oncology agents for the treatment of cancer, today announced financial results for the three and six months ended June 30, 2025, and highlighted recent pipeline progress and business updates.
“The first half of 2025 has been transformative for I-Mab,” said Sean Fu, PhD, Chief Executive Officer of I-Mab. “Our presentation at ESMO GI showcased compelling Phase 1b combination data for givastomig, reinforcing our confidence in its potential to be a best-in-class Claudin 18.2-directed therapy for metastatic gastric cancers in the 1L setting. Thanks to strong study momentum and active investigator engagement, we completed enrollment of the planned Phase 1b dose expansion cohorts ahead of schedule and expect to report topline data in Q1 2026. We believe our strong cash position and unwavering focus on value creation, position I-Mab to deliver meaningful clinical data and improve the lives of patients.”
Recent and Anticipated Upcoming Clinical Milestones
Givastomig (CLDN18.2 x 4-1BB bispecific):
Recent Developments:
- Positive Phase 1b Dose Escalation Data in Combination with Immunochemotherapy Presented at ESMO GI 2025 – Data from the dose escalation cohorts of the study were presented on July 2, 2025 in a Mini Oral presentation at the European Society for Medical Oncology Gastrointestinal Cancers Congress (ESMO GI) 2025 in Barcelona, Spain, accessible here. The data showed that givastomig in combination with immunochemotherapy demonstrated an
83% (10/12) objective response rate (ORR) at the doses (8 mg/kg and 12 mg/kg) selected for dose expansion. The responses were rapid, durable and deepened over time, with a favorable overall safety profile.
I-Mab hosted a virtual investor event on July 8, 2025 reviewing the Phase 1b dose escalation data (accessible for viewing here).
- Givastomig Monotherapy Data Published in Clinical Cancer Research – First-in-human monotherapy data for givastomig were published in Clinical Cancer Research, a journal of the American Association for Cancer Research (CCR), and a highly-ranked clinical oncology publication. The CCR paper details promising clinical data showing that givastomig monotherapy achieved an ORR of
16% in heavily pretreated Claudin 18.2-positive gastric cancer patients without encountering a dose limiting toxicity or maximum tolerated dose. The publication can be accessed here. The study provided the foundation for the ongoing Phase 1b combination study.
Upcoming Potential Clinical Milestones: I-Mab completed enrollment in the planned Phase 1b dose expansion study evaluating givastomig in combination with nivolumab and mFOLFOX6 for first line (1L) metastatic gastric cancers. The Company expects to present topline data in Q1 2026.
Other Programs: I-Mab anticipates updates in 2026 for ragistomig (PD-L1 x 4-1BB bispecific) and uliledlimab (monoclonal antibody targeting CD73), which are currently under development by ABL Bio and TJ Biopharma, respectively.
Corporate Developments
- I-Mab Announces Pricing of
$65 Million Underwritten Offering – I-Mab completed an underwritten offering of American Depositary Shares (ADSs) representing ordinary shares that raised total net proceeds of approximately$61.2 million . The offering included participation from new and existing investors including Everest Medicines, Janus Henderson Investors, Adage Capital Partners LP and Exome Asset Management.
- Givastomig Intellectual Property Portfolio Strengthened with Acquisition of Bridge Health – The acquisition provides I-Mab with upstream rights to the Claudin 18.2 parental antibody for use in bispecific and multi-specific applications, eliminates all royalty obligations and reduces future milestones for givastomig due to Bridge Health Biotech Co., Ltd. (Bridge Health) by I-Mab. The transaction is expected to close in Q3 2025.
Cash Position
As of June 30, 2025, the Company had cash and cash equivalents, and short-term investments of
As of June 30, 2025, the Company had 188,108,178 ordinary shares issued and outstanding, representing the equivalent of 81,786,164 ADSs, assuming the conversion of all ordinary shares into ADSs. In August 2025, the Company announced an underwritten offering of 76,666,659 ordinary shares, representing the equivalent of 33,333,330 ADSs.
Pro-forma for the underwritten offering, the Company had 264,774,837 ordinary shares issued and outstanding, representing the equivalent of 115,119,494 ADSs, assuming the conversion of all ordinary shares into ADSs.
Research and Development Expenses
Research and development (R&D) expenses were
Administrative Expenses
Administrative expenses were
Interest Income
Interest income was
Other Income (Expenses), Net
Other income (expenses), net were
Equity in Loss of Affiliates
Equity in loss of affiliates was
Net Loss from Continuing Operations
Net loss from continuing operations were (
Net Gain from Discontinued Operations
On April 2, 2024, the Company closed the divestiture of the Greater China assets and business operations announced on February 7, 2024 (the Transaction). In accordance with ASC 205-20, the Company determined that the Transaction represented a strategic shift that had a major effect on the business and therefore, met the criteria for classification as discontinued operations. As a result, the Company recognized a loss from discontinued operations of
Net Income (Loss)
Net income (loss) was
About Givastomig
Givastomig (TJ033721 / ABL111) is a bispecific antibody targeting Claudin 18.2 (CLDN18.2)-positive tumor cells. It conditionally activates T cells through the 4-1BB signaling pathway in the tumor microenvironment where CLDN18.2 is expressed. Givastomig is being developed for first line (1L) metastatic gastric cancers, with further potential in other solid tumors. In Phase 1 trials, givastomig has shown promising anti-tumor activity attributable to a potential synergistic effect of proximal interaction between CLDN18.2 on tumor cells and 4-1BB on T cells in the tumor microenvironment, while minimizing toxicities commonly seen with other 4-1BB agents.
An ongoing Phase 1b study is evaluating givastomig for the treatment of gastric cancer in the 1L setting in combination with standard of care, nivolumab (an anti-PD-1 checkpoint inhibitor) plus chemotherapy, in dose escalation (n=17) and dose expansion (n=40) cohorts. The study builds on positive Phase 1 monotherapy data.
Givastomig is being jointly developed through a global partnership with ABL Bio, in which I-Mab is the lead party and shares worldwide rights, excluding Greater China and South Korea, equally with ABL Bio.
About I-Mab
I-Mab (NASDAQ: IMAB) is a U.S.-based, global biotech company, focused on the development of precision immuno-oncology agents for the treatment of cancer. The Company’s differentiated pipeline is led by givastomig, a potential best-in-class, bispecific antibody (Claudin 18.2 x 4-1BB) designed to treat Claudin 18.2-positive gastric cancers. Givastomig conditionally activates T cells via the 4-1BB signaling pathway in the tumor microenvironment where Claudin 18.2 is expressed. Givastomig is being developed for first-line metastatic gastric cancers, with additional potential in other solid tumors. In Phase 1 trials, givastomig was observed to maintain strong tumor-binding and anti-tumor activity, attributable to a potential synergistic effect of proximal interaction with Claudin 18.2 and 4-1BB, while minimizing toxicities commonly seen with other 4-1BB agents.
For more information, please visit https://www.i-mabbiopharma.com and follow us on LinkedIn.
Forward Looking Statements
This announcement contains forward-looking statements. These statements are made under the “safe harbor” provisions of the U.S. Private Securities Litigation Reform Act of 1995. These forward-looking statements can be identified by terminology such as “will”, “expects”, “believes”, “designed to”, “anticipates”, “future”, “intends”, “plans”, “potential”, “estimates”, “confident”, and similar terms or the negative thereof. I-Mab may also make written or oral forward-looking statements in its periodic reports to the U.S. Securities and Exchange Commission (the “SEC”), in its annual report to shareholders, in press releases and other written materials and in oral statements made by its officers, directors or employees to third parties. Statements that are not historical facts, including statements about I-Mab’s beliefs and expectations, are forward-looking statements. Forward-looking statements in this press release include, without limitation, statements regarding: the potential benefits and clinical development of I-Mab’s drug candidates, including givastomig; anticipated clinical milestones and results, and related timing; the Company’s anticipated cash runway; the potential closing of the Bridge Health acquisition in Q3 2025. Forward-looking statements involve inherent risks and uncertainties that may cause actual results to differ materially from those contained in these forward-looking statements, including but not limited to the following: I-Mab’s ability to demonstrate the safety and efficacy of its drug candidates; the clinical results for its drug candidates, which may or may not support further development or New Drug Application/Biologics License Application (NDA/BLA) approval; the content and timing of decisions made by the relevant regulatory authorities regarding regulatory approval of I-Mab’s drug candidates; I-Mab’s ability to achieve commercial success for its drug candidates, if approved; I-Mab’s ability to obtain and maintain protection of intellectual property for its technology and drugs; I-Mab’s reliance on third parties to conduct drug development, manufacturing and other services; I-Mab’s limited operating history and I-Mab’s ability to obtain additional funding for operations and to complete the development and commercialization of its drug candidates; and those risks more fully discussed in the “Risk Factors” section in I-Mab’s annual report on Form 20-F filed with the SEC on April 3, 2025 as well as the discussions of potential risks, uncertainties, and other important factors in I-Mab’s subsequent filings with the SEC. All forward-looking statements are based on information currently available to I-Mab. I-Mab undertakes no obligation to publicly update or revise any forward-looking statements, whether as a result of new information, future events, or otherwise, except as may be required by law.
I-Mab Investor & Media Contacts
| PJ Kelleher | |
| LifeSci Advisors | |
| +1-617-430-7579 | |
| pkelleher@lifesciadvisors.com | |
| IR@imabbio.com |
| I-Mab Consolidated Balance Sheets (Unaudited; All amounts in thousands, except for par value and share data) | ||||||||
| As of | As of | |||||||
| June 30, 2025 | December 31, 2024 | |||||||
| Assets | ||||||||
| Current assets | ||||||||
| Cash and cash equivalents | $ | 165,404 | $ | 68,263 | ||||
| Short-term investments | 210 | 105,135 | ||||||
| Prepayments and other receivables | 2,026 | 3,295 | ||||||
| Total current assets | 167,640 | 176,693 | ||||||
| Property, equipment and software | 172 | 201 | ||||||
| Operating lease right-of-use assets | 3,209 | 3,597 | ||||||
| Investments at fair value, available-for-sale debt securities (amortized cost of | 34,468 | 30,824 | ||||||
| Other non-current assets | 1,219 | 1,365 | ||||||
| Total assets | $ | 206,708 | $ | 212,680 | ||||
| Liabilities and shareholders’ equity | ||||||||
| Current liabilities | ||||||||
| Accruals and other payables | $ | 6,494 | $ | 7,638 | ||||
| Operating lease liabilities, current | 853 | 816 | ||||||
| Total current liabilities | 7,347 | 8,454 | ||||||
| Operating lease liabilities, non-current | 2,628 | 3,066 | ||||||
| Total liabilities | 9,975 | 11,520 | ||||||
| Shareholders’ equity | ||||||||
| Ordinary shares ( | 19 | 19 | ||||||
| Treasury stock | (5,609 | ) | (6,225 | ) | ||||
| Additional paid-in capital | 1,459,977 | 1,460,021 | ||||||
| Accumulated other comprehensive income | 37,039 | 33,384 | ||||||
| Accumulated deficit | (1,294,693 | ) | (1,286,039 | ) | ||||
| Total shareholders’ equity | 196,733 | 201,160 | ||||||
| Total liabilities and shareholders’ equity | $ | 206,708 | $ | 212,680 | ||||
| I-Mab Consolidated Statements of Comprehensive Loss (Unaudited; All amounts in thousands, except for share and per share data) | ||||||||||||||||
| Three Months Ended June 30, | Six Months Ended June 30, | |||||||||||||||
| 2025 | 2024 | 2025 | 2024 | |||||||||||||
| Revenues | ||||||||||||||||
| Licensing and collaboration revenue | $ | — | $ | — | $ | — | $ | — | ||||||||
| Total revenues | — | — | — | — | ||||||||||||
| Expenses | ||||||||||||||||
| Research and development expenses(1) | (3,294 | ) | (5,203 | ) | (4,071 | ) | (11,265 | ) | ||||||||
| Administrative expenses(2) | (3,820 | ) | (11,937 | ) | (8,309 | ) | (14,378 | ) | ||||||||
| Total expenses | (7,114 | ) | (17,140 | ) | (12,380 | ) | (25,643 | ) | ||||||||
| Loss from operations | (7,114 | ) | (17,140 | ) | (12,380 | ) | (25,643 | ) | ||||||||
| Interest income | 1,800 | 2,131 | 3,672 | 2,840 | ||||||||||||
| Other income (expenses), net | (190 | ) | 6,067 | 54 | 5,480 | |||||||||||
| Equity in loss of affiliates(3) | — | — | — | (1,038 | ) | |||||||||||
| Loss from continuing operations before income tax expense | (5,504 | ) | (8,942 | ) | (8,654 | ) | (18,361 | ) | ||||||||
| Income tax expense | — | — | — | — | ||||||||||||
| Loss from continuing operations | (5,504 | ) | (8,942 | ) | (8,654 | ) | (18,361 | ) | ||||||||
| Discontinued operations: | ||||||||||||||||
| Loss from operations of discontinued operations(4) | — | — | — | (6,898 | ) | |||||||||||
| Income tax expense | — | — | — | — | ||||||||||||
| Gain on sale of discontinued operations | — | 34,364 | — | 34,364 | ||||||||||||
| Gain from discontinued operations | — | 34,364 | — | 27,466 | ||||||||||||
| Net income (loss) | (5,504 | ) | 25,422 | (8,654 | ) | 9,105 | ||||||||||
| Other comprehensive income (loss): | ||||||||||||||||
| Unrealized gain on available-for-sale debt securities, net of tax | $ | 3,644 | $ | — | $ | 3,644 | $ | — | ||||||||
| Foreign currency translation adjustments, net of tax | 8 | (348 | ) | 11 | 677 | |||||||||||
| Total comprehensive income (loss) | $ | (1,852 | ) | $ | 25,074 | $ | (4,999 | ) | $ | 9,782 | ||||||
| Weighted-average number of ordinary shares used in calculating net income (loss) per share | ||||||||||||||||
| - basic and diluted | 187,908,339 | 186,144,822 | 187,794,543 | 186,001,615 | ||||||||||||
| Net loss from continuing operations per share | ||||||||||||||||
| - basic and diluted | $ | (0.03 | ) | $ | (0.05 | ) | $ | (0.05 | ) | $ | (0.10 | ) | ||||
| Net income from discontinued operations per share | ||||||||||||||||
| - basic and diluted | $ | — | $ | 0.18 | $ | — | $ | 0.15 | ||||||||
| Net income (loss) per share - basic and diluted | $ | (0.03 | ) | $ | 0.13 | $ | (0.05 | ) | $ | 0.05 | ||||||
| Net loss from continuing operations per ADS(5) | ||||||||||||||||
| - basic and diluted | $ | (0.07 | ) | $ | (0.11 | ) | $ | (0.11 | ) | $ | (0.23 | ) | ||||
| Net income from discontinued operations per ADS(5) | ||||||||||||||||
| - basic and diluted | $ | — | $ | 0.42 | $ | — | $ | 0.34 | ||||||||
| Net income (loss) per ADS(5) - basic and diluted | $ | (0.07 | ) | $ | 0.31 | $ | (0.11 | ) | $ | 0.11 | ||||||
(1) Includes share-based compensation expense of
(2) Includes share-based compensation expense of
(3) Includes share-based compensation expense of
(4) Includes share-based compensation expense of
(5) Each 10 ADSs represents 23 ordinary shares.
FAQ
What were I-Mab's (IMAB) key clinical results for givastomig in Q2 2025?
How much cash does I-Mab (IMAB) have after its August 2025 offering?
When will I-Mab (IMAB) report topline data for givastomig's expansion study?
What was I-Mab's (IMAB) net loss in Q2 2025?
How long will I-Mab's (IMAB) current cash runway last?
