NovaBridge Reports Positive Phase 1b Results for Givastomig in Gastric Cancer with 77% Response Rate
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Jan 06 2026
0mins
Should l Buy NBP?
Source: Benzinga
- Clinical Trial Progress: NovaBridge's Phase 1b study evaluating givastomig in combination with nivolumab and mFOLFOX6 shows an overall response rate of 77% for the 8 mg/kg cohort and 73% for the 12 mg/kg cohort, indicating significant potential for this therapy in treating HER2-negative metastatic gastric cancer.
- Survival Data: The median progression-free survival (PFS) reached 16.9 months in the 8 mg/kg group, while PFS data for the 12 mg/kg group remains immature, highlighting the promising outlook of this treatment in extending patient survival.
- Safety Analysis: The combination therapy was generally well tolerated, with a safety profile comparable to standard care, and immune-related gastritis was observed to correlate with improved clinical outcomes, suggesting both safety and efficacy warrant attention.
- Future Research Plans: NovaBridge plans to initiate a global randomized Phase 2 study in Q1 2026 to evaluate both doses against standard care, with detailed Phase 1b dose expansion data expected to be presented at a medical conference later in 2026, further advancing the clinical development pipeline.
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Analyst Views on NBP
Wall Street analysts forecast NBP stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for NBP is 8.00 USD with a low forecast of 7.00 USD and a high forecast of 9.00 USD. However, analyst price targets are subjective and often lag stock prices, so investors should focus on the objective reasons behind analyst rating changes, which better reflect the company's fundamentals.
2 Analyst Rating
2 Buy
0 Hold
0 Sell
Moderate Buy
Current: 3.330
Low
7.00
Averages
8.00
High
9.00
Current: 3.330
Low
7.00
Averages
8.00
High
9.00
About NBP
Novabridge Biosciences is a global biotechnology platform company. The Company combines deep business development expertise with agile translational clinical development to identify, accelerate, and advance breakthrough assets. Its differentiated pipeline includes givastomig, a bispecific antibody (Claudin 18.2 x 4-1BB), and VIS-101, a 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. VIS-101 targets VEGF-A and ANG-2 to provide more potent and durable treatment benefits for patients with wet age-related macular degeneration (wet AMD) and diabetic macular edema (DME). VIS-101 is completing a large, randomized, dose-ranging Phase 2 study for wet AMD.
About the author

Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
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- Chairman's Purchase Plan: Fu Wei, Executive Chairman of NovaBridge Biosciences, intends to purchase up to $5 million in the company's ADSs through his controlled entity in open market transactions, reflecting confidence in the company's future growth.
- Positive Clinical Data: The recent positive dose expansion data for givastomig from the Phase 1b study reinforces NovaBridge's clinical development capabilities and market potential in treating gastric cancer.
- Global Platform Development: NovaBridge is committed to accelerating access to innovative medicines by combining deep business development expertise with agile clinical development, showcasing the strategic value of its global biotechnology platform.
- Diverse Pipeline: The company's pipeline includes potential best-in-class therapies like givastomig and VIS-101, targeting gastric cancer and other malignancies, demonstrating its diversity and innovation in the biopharmaceutical sector.
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- Clinical Trial Progress: NovaBridge's Phase 1b study evaluating givastomig in combination with nivolumab and mFOLFOX6 shows an overall response rate of 77% for the 8 mg/kg cohort and 73% for the 12 mg/kg cohort, indicating significant potential for this therapy in treating HER2-negative metastatic gastric cancer.
- Survival Data: The median progression-free survival (PFS) reached 16.9 months in the 8 mg/kg group, while PFS data for the 12 mg/kg group remains immature, highlighting the promising outlook of this treatment in extending patient survival.
- Safety Analysis: The combination therapy was generally well tolerated, with a safety profile comparable to standard care, and immune-related gastritis was observed to correlate with improved clinical outcomes, suggesting both safety and efficacy warrant attention.
- Future Research Plans: NovaBridge plans to initiate a global randomized Phase 2 study in Q1 2026 to evaluate both doses against standard care, with detailed Phase 1b dose expansion data expected to be presented at a medical conference later in 2026, further advancing the clinical development pipeline.
See More

- Significant Efficacy: NovaBridge's Phase 1b combination study of givastomig with nivolumab and chemotherapy in HER2-negative metastatic gastric cancer demonstrated an overall response rate of 77% at 8 mg/kg, indicating the potential to transform first-line treatment options.
- Extended Survival: The median progression-free survival reached 16.9 months at the 8 mg/kg dose, with a six-month landmark progression-free survival rate of 73%, providing patients with a longer survival period and enhancing the clinical value of the therapy.
- Good Safety Profile: The combination therapy exhibited a safety profile comparable to current standard-of-care treatments, demonstrating good tolerability, which may position it as a viable option for future therapies and improve patient treatment experiences.
- Stock Price Surge: NovaBridge's shares rose over 11% in pre-market trading after closing at $4.37, up 2.34%, reflecting the market's positive reaction to the study results and potentially attracting more investor interest in its future developments.
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- Industry Leadership: NovaBridge's inclusion in the Nasdaq Biotech Index on December 19, 2025, significantly enhances the company's visibility and reinforces its position as a leader in the biotechnology sector.
- Opening Bell Ceremony: Executive Chairman Fu Wei will ring the Nasdaq Opening Bell on January 2, 2026, alongside the management team, symbolizing the company's successful transition to a global biotech platform and aiming to enhance shareholder value.
- Innovative Drug Pipeline: NovaBridge's pipeline includes the potential best-in-class drug givastomig for gastric cancer and VIS-101 for wet age-related macular degeneration, showcasing the company's robust capabilities in innovative drug development.
- Strategic Vision: CEO Sean Fu emphasized that joining the Nasdaq Biotech Index marks the success of NovaBridge's strategic vision, which is expected to accelerate the development of innovative medicines and drive future growth for the company.
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