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NovaBridge to Present at the Leerink Partners 2026 Global Healthcare Conference

MWN-AI** Summary

NovaBridge Biosciences (Nasdaq: NBP), a leading global biotechnology platform, is set to present at the forthcoming Leerink Partners 2026 Global Healthcare Conference, taking place from March 8-11, 2026. The company’s management team will engage in a fireside chat format on March 11 at 8:00 AM ET, which will be accessible via webcast. The presentation will be available on the NovaBridge website for 90 days, allowing a broader audience to gain insights into the company’s innovative approaches and pipelines.

Dedicated to enhancing access to breakthrough therapies, NovaBridge expertly integrates business development with agile clinical advancement. The company is particularly known for its promising drug candidates, including givastomig, a Claudin 18.2 x 4-1BB bispecific antibody. Givastomig shows potential as a best-in-class treatment for Claudin 18.2-positive gastric cancer, currently under evaluation in a global Phase 2 study, bolstered by positive results from a prior Phase 1b trial.

Additionally, NovaBridge is collaborating with ABL Bio on ragistomig, another bispecific antibody aimed at solid tumors, while also controlling global rights outside certain regions for uliledlimab, an anti-CD73 antibody that targets cancer-related immunosuppression.

Their innovative pipeline also includes VIS-101, a biologic targeting VEGF-A and ANG-2, which is undergoing Phase 2a trials for treating wet age-related macular degeneration. As NovaBridge focuses on bridging scientific discovery with patient needs, its diverse drug development portfolio positions it as a significant player in the biotechnology landscape.

For more information, visit NovaBridge's website or connect with them on LinkedIn.

MWN-AI** Analysis

As NovaBridge Biosciences prepares for its presentation at the Leerink Partners 2026 Global Healthcare Conference, investors should consider the strategic insights and positive developments articulated during the event. The company is at a pivotal stage, particularly with its lead candidate, givastomig, which has displayed promising results in early clinical trials for gastric cancer. The upcoming Phase 2 study will be crucial, and positive outcomes could significantly bolster investor confidence and elevate stock prices.

Investors should closely watch the discussions surrounding givastomig's mechanism of action and how it positions itself as a potential leader in the treatment of Claudin 18.2-positive malignancies. The differentiation of NovaBridge's pipeline, including the promising VIS-101 for wet age-related macular degeneration, should be highlighted as well. These assets underline NovaBridge’s strategy of targeting significant unmet medical needs, which can enhance their attractiveness in a competitive marketplace.

Additionally, the collaboration with ABL Bio on ragistomig presents an exciting avenue for growth. The integration of PD-L1 and 4-1BB pathways demonstrates a sophisticated approach to cancer treatment that may appeal to a broader investor base seeking biotech companies that innovate beyond traditional methods.

Given the company’s leadership in developing transformative therapies and its robust pipeline, NovaBridge shows considerable investment potential. However, prospective investors should remain vigilant about the inherent risks of biotechnology investments, particularly the volatility associated with clinical trial results. As the healthcare conference approaches, it would be prudent to monitor market reactions to any data or strategic updates provided by NovaBridge's management, as these could influence short-term trading strategies.

In summary, NovaBridge presents a compelling investment case as it positions itself for potential breakthroughs in oncology and ophthalmology, but investors should approach with due diligence, considering both the opportunities and risks involved.

**MWN-AI Summary and Analysis is based on asking OpenAI to summarize and analyze this news release.

Source: GlobeNewswire

ROCKVILLE, Md., March 02, 2026 (GLOBE NEWSWIRE) -- NovaBridge Biosciences (Nasdaq: NBP) (NovaBridge or the Company) a global biotechnology platform company committed to accelerating access to innovative medicines, today announced that NovaBridge’s management team will participate in the upcoming Leerink Partners 2026 Global Healthcare Conference being held on March 8-11, 2026.

Conference details are as follows:

Leerink Partners Global Healthcare Conference
Format: Fireside Chat
Date: Wednesday, March 11, 2026
Time: 8:00 AM ET
Webcast Link: Here

The webcast of the company presentation will be accessible on the News & Events page of the NovaBridge website for 90 days.

About NovaBridge

NovaBridge is a global biotechnology platform company committed to accelerating access to innovative medicines. The Company combines deep business development expertise with agile translational clinical development to identify, accelerate, and advance breakthrough assets. By bridging science, strategy, and execution, NovaBridge enables transformative therapies to progress rapidly from discovery toward patients in need.

The Company’s differentiated pipeline is led by givastomig, a potential best-in-class, Claudin 18.2 x 4-1BB bispecific antibody, and VIS-101, a potential best-in-class bifunctional biologic, targeting VEGF-A and ANG2.

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 to treat Claudin 18.2-positive gastric cancer and other gastrointestinal malignancies. The product candidate is being evaluated in a global, randomized Phase 2 study, following the recent announcement of positive topline results from a Phase 1b, multi-center, open label study in first line gastric cancer. The Company is also collaborating with its partner, ABL Bio, for the development of ragistomig, a bispecific antibody integrating PD-L1 as a tumor engager and 4-1BB as a conditional T cell activator, in solid tumors. Additionally, NovaBridge owns worldwide rights outside of China to uliledlimab, an anti-CD73 antibody that targets adenosine-driven immunosuppression in cancer.

VIS-101 targets VEGF-A and ANG-2 to provide more potent and durable treatment benefits for patients with wet age-related macular degeneration and diabetic macular edema. VIS-101 is currently completing a randomized, dose-ranging Phase 2a study for wet AMD. NovaBridge is the majority shareholder of Visara, Inc., and Visara controls global rights to VIS-101, outside of Greater China and certain countries in Asia.

For more information, please visit www.novabridge.com and follow us on LinkedIn.

NovaBridge Investor & Media Contacts

PJ Kelleher
LifeSci Advisors
+1-617-430-7579
pkelleher@lifesciadvisors.com

NovaBridge Biosciences
+1-240-745-6330
IR@novabridge.com 


FAQ**

How does NovaBridge's collaboration with ABL Bio on ragistomig compare to other partnerships in the biotech sector, specifically related to I-MAB IMAB's strategies for immuno-oncology treatment development?

NovaBridge's collaboration with ABL Bio on ragistomig stands out in the biotech sector for its focused approach on innovative immuno-oncology solutions, similar to I-MAB's strategies, but diverges in tactical alignment and target demographics for treatment development.

Given the promising results from the Phase 1b study of givastomig, what are the projected timelines for further development, and how will this impact I-MAB IMAB's competitive positioning in the market?

Projected timelines for further development of givastomig will likely depend on results from subsequent trials, but positive momentum could enhance I-MAB IMAB’s competitive positioning in the market by attracting partnerships and investment, and potentially accelerating market entry.

Can NovaBridge elaborate on how the differentiation of VIS-101 targeting VEGF-A and ANG-2 aligns with I-MAB IMAB's therapeutic focus in ophthalmology and oncology?

NovaBridge can explain that VIS-101's dual targeting of VEGF-A and ANG-2 complements I-MAB IMAB's therapeutic focus by addressing critical pathways in angiogenesis and inflammation, enhancing therapeutic efficacy in both ophthalmology and oncology contexts.

What contingency plans does NovaBridge have in place if the Phase 2 studies yield mixed results, and how will that affect investor confidence, especially considering trends seen with I-MAB IMAB?

NovaBridge has established adaptive trial designs and alternative development pathways to mitigate risks from mixed Phase 2 results, which could bolster investor confidence by demonstrating proactive management, similar to strategies employed by I-MAB (IMAB).

**MWN-AI FAQ is based on asking OpenAI questions about NovaBridge Biosciences Sponsored ADS (NASDAQ: NBP).

NovaBridge Biosciences Sponsored ADS

NASDAQ: NBP

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