Welcome to our dedicated page for I-Mab news (Ticker: IMAB), a resource for investors and traders seeking the latest updates and insights on I-Mab stock.
I-Mab (NASDAQ: IMAB), now known as NovaBridge Biosciences, generates a steady flow of news as a U.S.-based, global biotech company focused on precision immuno-oncology. Investors following IMAB-related headlines can track how the company advances its lead Claudin 18.2 x 4-1BB bispecific antibody, givastomig, and other pipeline assets through clinical milestones, strategic transactions, and capital markets activity.
News coverage commonly highlights clinical data from Phase 1 and Phase 1b studies of givastomig in Claudin 18.2-positive gastric and gastroesophageal cancers, including monotherapy results and combination regimens with immunochemotherapy in the first-line metastatic setting. Company announcements describe objective response rates, safety findings, and study design details from presentations at major oncology conferences such as ESMO GI and the AACR-NCI-EORTC Molecular Targets and Cancer Therapeutics meeting.
Beyond clinical readouts, IMAB news items also cover the company’s broader transformation into a global biotech platform under the NovaBridge Biosciences name. Releases discuss the adoption of a hub-and-spoke business model, the formation of subsidiaries like Visara, Inc. for VIS-101 in ophthalmology, and strategic agreements with partners including ABL Bio, AffaMed Therapeutics, AskGene Pharma, and Everest Medicines. Capital markets updates, such as underwritten offerings of American Depositary Shares and intentions to pursue a dual listing on the Hong Kong Stock Exchange, are also key themes.
On this news page, readers can review company press releases, SEC-referenced announcements, and other IMAB-related updates in one place. For investors and researchers, regularly checking this feed offers insight into clinical progress, partnership activity, governance changes, and financing events that shape the outlook for I-Mab’s, and NovaBridge Biosciences’, oncology and ophthalmology programs.
I-Mab (NASDAQ: IMAB) reported Q3 2024 financial results and pipeline updates. The company ended Q3 with $184.4 million in cash and equivalents, expecting runway into 2027. Key developments include the appointment of Dr. Sean Fu as permanent CEO and encouraging clinical data for givastomig presented at ESMO 2024. The company reported a net loss from continuing operations of $20.5 million for Q3 2024. R&D expenses were $4.5 million, down from $5.1 million in Q3 2023. The company is preparing for a Phase 2 study of uliledlimab in first-line mNSCLC, with first patient dosing expected in 1H 2025.
I-Mab (NASDAQ: IMAB) has appointed Sean Fu, PhD, MBA as permanent Chief Executive Officer effective November 1, 2024, following his interim CEO role since July 15, 2024. Dr. Fu brings over 20 years of life sciences industry experience, including roles as Operating Partner at ABio-X, co-founder and CEO of RVAC Medicines, and Group VP at Luye Pharma Group. He previously spent 15 years at Merck & Co., managing late-stage clinical portfolio finances and leading R&D network integration following the $42 billion Merck-Schering-Plough merger. Dr. Fu holds a PhD from Ohio State University and an MBA from Wharton.
I-Mab (NASDAQ: IMAB) announced it will release its Q3 2024 financial results on November 14, 2024, before the US market opens. The company will not hold a conference call for Q3 results but plans to host an investor update call with its full-year 2024 results, where it will discuss its clinical pipeline, corporate strategy, and objectives. Financial results and related information will be available on the company's website.
I-Mab (NASDAQ: IMAB) announced it will present Phase 1 optimized dose estimation data for givastomig (TJ033721/ABL111) at SITC 2024. The presentation focuses on this novel first-in-class Claudin18.2 and 4-1BB bispecific antibody for cancer treatment. The poster presentation, numbered 1474, will take place on November 9, 2024, at the George R. Brown Convention Center in Houston, Texas, during the Society for Immunotherapy of Cancer conference. The poster details optimal dose estimation using an integrated approach from Phase 1 data and will be available on I-Mab's website under the 'Innovation, Publications & Presentations' section.
I-Mab (NASDAQ: IMAB), a US-based global biotech company focused on cancer immunotherapies, has announced its participation in the Truist Securities BioPharma Symposium on November 7, 2024. The company's management team, including Interim CEO Sean Fu, CFO Joe Skelton, CMO Phillip Dennis, and Senior Director of Investor Relations Tyler Ehler, will engage in one-on-one and small group meetings with investors during the event.
I-Mab (NASDAQ: IMAB) presented updated Phase 1 data for givastomig, a novel Claudin 18.2 X 4-1BB bispecific antibody immunostimulant, at ESMO 2024. The study showed promising single-agent activity in heavily pre-treated gastric cancer patients with varying Claudin 18.2 expression levels. Key findings include:
- Recommended Phase 2 dose: 8-12 mg/kg
- Well-tolerated up to highest study doses
- Objective response rate (ORR): 16.3% (7/43 patients)
- Disease control rate (DCR): 48.8% (21/43 patients)
- No dose-limiting toxicity up to 15 mg/kg Q2W and 18 mg/kg Q3W
- Linear pharmacokinetics at doses ≥5 mg/kg
A Phase 1b study combining givastomig with standard-of-care treatment in front-line gastric cancer patients is ongoing, with results expected in H2 2025.
I-Mab (NASDAQ: IMAB) presented positive pharmacokinetics data for uliledlimab, a CD73-targeting antibody, at the 2024 World Conference on Lung Cancer. The data, derived from three Phase 1 studies, supports dosing strategies for upcoming clinical trials. Key findings include:
- 95% of the simulated population achieved target threshold with 30 mg/kg of uliledlimab
- Positive correlation between uliledlimab concentration and overall response rate probability in mNSCLC patients
- CD73 receptor occupancy in peripheral B cells reached and maintained at 90% or above
- 30 mg/kg dose with a single boost on C1D8 maintained target concentration of 80 μg/mL
A randomized Phase 2 study of uliledlimab combined with pembrolizumab and chemotherapy is expected to begin in 1H 2025.
I-Mab reported its 1H 2024 financial results and provided pipeline updates:
- Completed divestiture of China operations
- Received IND clearance for uliledlimab (CD73 antibody) in first-line mNSCLC
- Entered clinical collaboration with Bristol Myers Squibb for givastomig (CLDN18.2 X 4-1BB bispecific) in gastric cancer
- Presented encouraging early data for ragistomig (PD-L1 X 4-1BB bispecific) at ASCO 2024
- Cash position of $207.5 million as of June 30, 2024, with runway into 2027
- Net loss from continuing operations of $17.8 million for 1H 2024
- No revenue generated in 1H 2024
- R&D expenses of $10.8 million and administrative expenses of $14.3 million for 1H 2024
I-Mab (NASDAQ: IMAB), a US-based global clinical-stage biotech company focused on developing immunotherapies for cancer treatment, has announced its participation in the H.C. Wainwright 26th Annual Global Investment Conference on September 10, 2024. The company's management team, including Interim CEO Sean Fu and CMO Phillip Dennis, will present at 5:00 PM ET.
The event will also feature one-on-one and small group meetings from September 9-10, with additional management participants including CFO Joe Skelton and Senior Director of Investor Relations Tyler Ehler. A webcast of the presentation will be available on I-Mab's IR website under the 'Event Calendar' section.
I-Mab (NASDAQ: IMAB), a US-based global biotech company focused on developing immunotherapies for cancer treatment, has announced it will release its 1H 2024 financial results on August 28, 2024. The company will host a conference call and webcast at 8:00 AM ET on the same day to discuss financial results, pipeline progress, and recent business highlights for the half year ended June 30, 2024.
Investors and analysts can join the conference call via domestic (1-877-407-0784) or international (1-201-689-8560) dial-in numbers, using the Conference ID: 13747695. A webcast link is also provided. The Call me™ link will be active 15 minutes before the scheduled start time. A replay of the call will be available on the I-Mab website's Investor Relations page for 6 months.