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NovaBridge Biosciences

Full company profile

uuid0044swq

Namestring
NovaBridge Biosciences
Legal namestring
NovaBridge Biosciences
Websiteurl
novabridge.com
Company typeenum
Public
Founded yearint
2016
Descriptiontext

NovaBridge Biosciences (NASDAQ: NBP), formerly I-Mab Biopharma, is a clinical-stage biopharmaceutical company founded in 2016 and headquartered in Rockville, Maryland, that operates a Hub-and-Spoke platform dedicated to bringing Asian innovative medicines to global markets. The company is backed by CBC Group (formerly C-Bridge Capital), Asia's largest healthcare-dedicated asset management firm, whose CEO Fu Wei serves as Executive Chairman. As of December 31, 2025, NovaBridge held $210.8 million in cash supporting operations through 2028 and reported a FY2025 net loss of $88.3 million, with no approved products or commercial revenue.

The company's pipeline is built on proprietary bispecific antibody platform technology spanning immuno-oncology and ophthalmology. Lead oncology asset givastomig is a CLDN18.2 x 4-1BB bispecific antibody with silenced FC (IgG1) for conditional T cell activation, targeting first-line HER2-negative metastatic gastric cancer; it holds FDA Fast Track Designation, FDA-confirmed accelerated approval pathway eligibility, and FDA Orphan Drug Designation, with a registrational Phase 3 trial planned for Q4 2026. Additional oncology assets include ragistomig (PD-L1 x 4-1BB bispecific, developed with ABL Bio's Grabody-T platform) and uliledlimab (anti-CD73 monoclonal antibody). In ophthalmology, subsidiary Visara, Inc. is advancing VIS-101, a tetravalent VEGF-A x ANG-2 bispecific antibody for wet AMD, DME, and RVO, with Phase 2a data showing >10 ETDRS letters visual acuity improvement and approximately 50% of patients retreatment-free at six months.

NovaBridge is pre-revenue and expects future revenue from pharmaceutical product sales upon regulatory approval, distributed through specialty pharmacy and hospital channels. The company is preparing commercial capabilities through the appointment of a President and Chief Commercial Officer (Mark Hagler, April 2026) and a new CEO (Dr. Srishti Gupta, July 2026) with prior operational turnaround experience at Idorsia Ltd. The company maintains operational offices in the US (Rockville, Needham, Short Hills) and Asia (Hong Kong, Shanghai), and co-develops assets with strategic partners ABL Bio and Everest Medicines.

Short descriptiontext

NovaBridge Biosciences is a clinical-stage biopharmaceutical company operating a Hub-and-Spoke platform to develop and globalize bispecific antibody therapeutics in immuno-oncology (givastomig, ragistomig, uliledlimab) and ophthalmology (VIS-101), serving patients with gastric cancer and retinal vascular diseases.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersRockville, United States
HQ citystring
Rockville
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices5 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
bispecific antibody therapeutics, immuno-oncology drug development, clinical-stage biopharmaceuticals, ophthalmic biologics, oncology pipeline drugs
Industry4 codes
1Antibody Discovery & Engineering Platforms (display tech, bispecifics, Fc engineering)
CodeHLAAAIABPrimaryYes
2Bispecific & Multispecific Antibodies
CodeHLAAAAAFPrimaryNo
3Gastroenterology Specialty Pharmaceuticals
CodeHLAIACAEPrimaryNo
4Oncology & Hematology Pharmaceuticals
CodeHLAIAAACPrimaryNo
NAICS code4 codes
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
  • Biological Product (except Diagnostic) Manufacturing325414
  • Pharmaceutical and Medicine Manufacturing3254
  • Scientific Research and Development Services5417
SIC code3 codes
  • Pharmaceutical Preparations2834
  • Biological Products, (No Disgnostic Substances)2836
  • Services-Commercial Physical & Biological Research8731
Product category
Clinical-Stage Biopharmaceuticals
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Pharmaceutical Product Revenue
TypeOne Time License
Description

NovaBridge is a pre-revenue clinical-stage biopharmaceutical company. The company expects to generate revenue from sales of approved drug candidates, primarily givastomig for gastric cancer and VIS-101 for wet AMD, once regulatory approvals are obtained. The company maintains $210.8M in cash as of December 31, 2025, providing runway through 2028.

biospace.com
Marketing channels4 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components4 values
Technology or R&D, Personnel, Operations, Marketing or Sales
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

NovaBridge Biosciences is a clinical-stage biopharmaceutical company developing bispecific antibody therapeutics for oncology and ophthalmology indications. The company's pipeline includes givastomig (CLDN18.2 x 4-1BB bispecific antibody) for first-line HER2-negative metastatic gastric cancer, VIS-101 (VEGF-A x ANG-2 bispecific antibody) for retinal vascular diseases, ragistomig (PD-L1 x 4-1BB), and uliledlimab (anti-CD73 mAb). The company operates a Hub-and-Spoke platform linking Asian innovative medicines to global markets, backed by CBC Group.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • 75% objective response rate and 16.9-month median progression-free survival in Phase 1b givastomig study
+2 more records
Product and service4 records
1Givastomig
CategoryBispecific Antibody Oncology Therapeutics
Description

A Claudin 18.2 x 4-1BB bispecific antibody that conditionally activates T cells through the 4-1BB signaling pathway in the tumor microenvironment where CLDN18.2 is expressed. Features silenced FC (IgG1) to minimize unintended systemic immune activation and conditional 4-1BB agonist activity for localized T cell activation. In development for HER2-negative, CLDN18.2+, PD-L1+ metastatic gastric/gastroesophageal adenocarcinoma in combination with nivolumab and chemotherapy. Demonstrated 75% objective response rate and 16.9-month median progression-free survival in Phase 1b trials. Received FDA Fast Track Designation and FDA Orphan Drug Designation.

2VIS-101
CategoryBispecific Antibody Ophthalmic Therapeutics
Description

A tetravalent dual VEGF-A x ANG-2 bispecific antibody designed for retinal vascular diseases including wet age-related macular degeneration (wet AMD), diabetic macular edema (DME), and retinal vein occlusion (RVO). Features humanized anti-VEGF-A mAb with approximately 2X inhibitory activity, optimized Fc region for shortened plasma half-life, and anti-Ang-2 inhibitory peptides (18mers) with approximately 17X inhibitory activity for class-leading durability. Achieved >10 ETDRS letters mean visual acuity improvement in Phase 2a wet AMD study, with approximately half of patients remaining retreatment-free at six months. Developed under the Visara, Inc. subsidiary.

3Ragistomig
CategoryBispecific Antibody Oncology Therapeutics
Description

A PD-L1 x 4-1BB bispecific antibody using ABL Bio's 'Grabody-T' platform. Uses the PD-L1 arm as tumor-dependent T-cell activator and the 4-1BB arm as conditional T cell activator upon tumor engagement, stimulating 4-1BB activation only in the presence of PD-L1 expressing tumor cells to minimize off-tumor toxicity. In development for solid tumors including non-small cell lung cancer in combination with PD-(L)1 inhibitors. Being jointly developed through a global partnership with ABL Bio.

4Uliledlimab
CategoryMonoclonal Antibody Oncology Therapeutics
Description

A differentiated, humanized anti-CD73 monoclonal antibody that targets the CD73 ecto-enzyme which converts extracellular AMP to adenosine in the tumor microenvironment. Features a unique intra-dimer binding mechanism leading to differentiated and favorable functional properties for suppressing tumor growth in combination with checkpoint therapies. Developed for solid tumors with adenosine-driven immunosuppression.

Scale indicator6 records

Each record includes

Type, Value, Description, Source

Partnership4 partners
Strategic tierCoreTypeStrategic or Co-development Partner
Description

ABL Bio is a global biotechnology company and key development partner for givastomig (ABL111) and ragistomig (ABL503). Givastomig is being jointly developed through a global partnership with ABL Bio, where NovaBridge is the lead party and shares worldwide rights excluding Greater China and South Korea equally with ABL Bio. Ragistomig (TJ-L14B/ABL503) uses ABL Bio's 'Grabody-T' bispecific antibody platform technology.

Strategic tierMajorTypeStrategic or Co-development Partner
Description

Everest Medicines holds regional rights to VIS-101 in Greater China and certain Asian territories. Visara (NovaBridge majority-owned subsidiary) grants Everest Medicines exclusive license for development and commercialization of VIS-101 outside NovaBridge's retained territories.

Strategic tierMinorTypeStrategic or Co-development Partner
Description

ABio-X is shown as a partner logo on NovaBridge's website. Dr. Sean Cao co-founded ABio-X Holdings and serves as director.

Strategic tierMinorTypeStrategic or Co-development Partner
Description

TJ Biopharma is shown as a partner logo on NovaBridge's website. Chun Kwok Alan Au serves as independent non-executive director of TJ Biopharma since January 2021.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Clinical-stage biotech with proprietary bispecific antibody platforms (Aziyo and EFECT) used to develop oncology candidates. Highly comparable to NovaBridge's platform-based approach to building a multi-asset bispecific pipeline.

TypeDirect peer
Description

Industry leader in bispecific antibody technology (Duobody platform) and developer of multiple approved and clinical-stage bispecifics in oncology. Comparable to NovaBridge as a developer of differentiated bispecific antibody therapeutics targeting immuno-oncology indications.

TypeBroad incumbent
Description

Broad biopharmaceutical incumbent and the dominant competitor in retinal vascular disease treatment with Eylea/Eylea HD in the wet AMD/DME market where NovaBridge's VIS-101 will compete. Includes Regeneron to frame VIS-101's competitive landscape.

TypeRegional player
Description

Asia-region-focused clinical and commercial biopharma with regional rights to NovaBridge's VIS-101 (VEGF-A x ANG-2) for Greater China and selected Asian territories. Operates a similar model of bringing innovative therapeutics into the Asia-Pacific market.

TypeEmerging player
Description

Clinical-stage oncology biotech developing bispecific antibodies (e.g., CTX-009, CTX-112) with checkpoint and tumor-targeted mechanisms comparable to NovaBridge's 4-1BB-based bispecifics. Similar early-stage platform with multiple oncology indications.

TypeDirect peer
Description

China-headquartered clinical-stage bispecific antibody developer with multiple oncology assets (e.g., ivonescimab, cadonilimab) and a similar Asia-origin model of advancing innovative biologics globally. Strong overlap with NovaBridge's oncology bispecific strategy and Asian biotech positioning.

TypeDirect peer
Description

South Korea-based clinical-stage biotech developing bispecific antibodies using the Grabody-T platform, which is the same technology underlying NovaBridge's givastomig and ragistomig. ABL Bio is a co-development partner and most directly comparable peer in bispecific antibody design and pipeline.

TypeDirect peer
Description

Clinical-stage oncology biotech developing bispecific antibodies (e.g., DART and TRIDENT platforms) for solid tumors, including PD-L1 x 4-1BB and other immuno-oncology targets that overlap with NovaBridge's ragistomig and givastomig mechanisms.

TypeEmerging player
Description

Clinical-stage oncology biotech developing multiple targeted therapies (including CLDN18.2 and immuno-oncology assets) with a hub-style pipeline approach similar to NovaBridge's structure. Comparable as a multi-asset oncology biotech.

TypeEmerging player
Description

Clinical-stage biotech with POWERbody masked antibody platform developing bispecifics and ADCs for oncology, with a comparable China-Asia origin and clinical-stage profile. Overlaps with NovaBridge's approach to engineering differentiated antibody formats.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile2 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature4 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles15 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

Subsidiaries1 record

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

NovaBridge Biosciences

Clinical-Stage Biopharmaceuticalsnovabridge.com

NovaBridge Biosciences is a clinical-stage biopharmaceutical company operating a Hub-and-Spoke platform to develop and globalize bispecific antibody therapeutics in immuno-oncology (givastomig, ragistomig, uliledlimab) and ophthalmology (VIS-101), serving patients with gastric cancer and retinal vascular diseases.

What NovaBridge Biosciences does

NovaBridge Biosciences (NASDAQ: NBP), formerly I-Mab Biopharma, is a clinical-stage biopharmaceutical company founded in 2016 and headquartered in Rockville, Maryland, that operates a Hub-and-Spoke platform dedicated to bringing Asian innovative medicines to global markets. The company is backed by CBC Group (formerly C-Bridge Capital), Asia's largest healthcare-dedicated asset management firm, whose CEO Fu Wei serves as Executive Chairman. As of December 31, 2025, NovaBridge held $210.8 million in cash supporting operations through 2028 and reported a FY2025 net loss of $88.3 million, with no approved products or commercial revenue.

The company's pipeline is built on proprietary bispecific antibody platform technology spanning immuno-oncology and ophthalmology. Lead oncology asset givastomig is a CLDN18.2 x 4-1BB bispecific antibody with silenced FC (IgG1) for conditional T cell activation, targeting first-line HER2-negative metastatic gastric cancer; it holds FDA Fast Track Designation, FDA-confirmed accelerated approval pathway eligibility, and FDA Orphan Drug Designation, with a registrational Phase 3 trial planned for Q4 2026. Additional oncology assets include ragistomig (PD-L1 x 4-1BB bispecific, developed with ABL Bio's Grabody-T platform) and uliledlimab (anti-CD73 monoclonal antibody). In ophthalmology, subsidiary Visara, Inc. is advancing VIS-101, a tetravalent VEGF-A x ANG-2 bispecific antibody for wet AMD, DME, and RVO, with Phase 2a data showing >10 ETDRS letters visual acuity improvement and approximately 50% of patients retreatment-free at six months.

NovaBridge is pre-revenue and expects future revenue from pharmaceutical product sales upon regulatory approval, distributed through specialty pharmacy and hospital channels. The company is preparing commercial capabilities through the appointment of a President and Chief Commercial Officer (Mark Hagler, April 2026) and a new CEO (Dr. Srishti Gupta, July 2026) with prior operational turnaround experience at Idorsia Ltd. The company maintains operational offices in the US (Rockville, Needham, Short Hills) and Asia (Hong Kong, Shanghai), and co-develops assets with strategic partners ABL Bio and Everest Medicines.

NovaBridge Biosciences firmographics

Firmographics
Name
NovaBridge Biosciences
Legal name
NovaBridge Biosciences
Website
https://novabridge.com
Company type
Public
Founded year
2016
Operating status
Operating
Headcount range
11–50 employees
Short description
NovaBridge Biosciences is a clinical-stage biopharmaceutical company operating a Hub-and-Spoke platform to develop and globalize bispecific antibody therapeutics in immuno-oncology (givastomig, ragistomig, uliledlimab) and ophthalmology (VIS-101), serving patients with gastric cancer and retinal vascular diseases.
Ownership category
akta.pro rank

NovaBridge Biosciences industry classification

Industry
Product category
Clinical-Stage Biopharmaceuticals
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714), Biological Product (except Diagnostic) Manufacturing (325414), Pharmaceutical and Medicine Manufacturing (3254), Scientific Research and Development Services (5417)
SIC
Pharmaceutical Preparations (2834), Biological Products, (No Disgnostic Substances) (2836), Services-Commercial Physical & Biological Research (8731)
akta.pro primary industry
Antibody Discovery & Engineering Platforms (display tech, bispecifics, Fc engineering) (HLAAAIAB)
akta.pro secondary industries
Bispecific & Multispecific Antibodies (HLAAAAAF), Gastroenterology Specialty Pharmaceuticals (HLAIACAE), Oncology & Hematology Pharmaceuticals (HLAIAAAC)

Keywords

  • Bispecific antibody therapeutics
  • Immuno-oncology drug development
  • Clinical-stage biopharmaceuticals
  • Ophthalmic biologics
  • Oncology pipeline drugs

Where NovaBridge Biosciences is headquartered

Location

Headquarters

HQ city
Rockville
HQ country
United States
HQ region
North America

Offices5 records

Markets served

NovaBridge Biosciences business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Personnel, Operations, Marketing or Sales

Revenue model

  1. Pharmaceutical Product Revenue: NovaBridge is a pre-revenue clinical-stage biopharmaceutical company. The company expects to generate revenue from sales of approved drug candidates, primarily givastomig for gastric cancer and VIS-101 for wet AMD, once regulatory approvals are obtained. The company maintains $210.8M in cash as of December 31, 2025, providing runway through 2028.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels4 records

NovaBridge Biosciences product offering

Product offering

Core offering

NovaBridge Biosciences is a clinical-stage biopharmaceutical company developing bispecific antibody therapeutics for oncology and ophthalmology indications. The company's pipeline includes givastomig (CLDN18.2 x 4-1BB bispecific antibody) for first-line HER2-negative metastatic gastric cancer, VIS-101 (VEGF-A x ANG-2 bispecific antibody) for retinal vascular diseases, ragistomig (PD-L1 x 4-1BB), and uliledlimab (anti-CD73 mAb). The company operates a Hub-and-Spoke platform linking Asian innovative medicines to global markets, backed by CBC Group.

Differentiator

Problem solved

Functional benefit

Products and services

  • Givastomig A Claudin 18.2 x 4-1BB bispecific antibody that conditionally activates T cells through the 4-1BB signaling pathway in the tumor microenvironment where CLDN18.2 is expressed. Features silenced FC (IgG1) to minimize unintended systemic immune activation and conditional 4-1BB agonist activity for localized T cell activation. In development for HER2-negative, CLDN18.2+, PD-L1+ metastatic gastric/gastroesophageal adenocarcinoma in combination with nivolumab and chemotherapy. Demonstrated 75% objective response rate and 16.9-month median progression-free survival in Phase 1b trials. Received FDA Fast Track Designation and FDA Orphan Drug Designation.
  • VIS-101 A tetravalent dual VEGF-A x ANG-2 bispecific antibody designed for retinal vascular diseases including wet age-related macular degeneration (wet AMD), diabetic macular edema (DME), and retinal vein occlusion (RVO). Features humanized anti-VEGF-A mAb with approximately 2X inhibitory activity, optimized Fc region for shortened plasma half-life, and anti-Ang-2 inhibitory peptides (18mers) with approximately 17X inhibitory activity for class-leading durability. Achieved >10 ETDRS letters mean visual acuity improvement in Phase 2a wet AMD study, with approximately half of patients remaining retreatment-free at six months. Developed under the Visara, Inc. subsidiary.
  • Ragistomig A PD-L1 x 4-1BB bispecific antibody using ABL Bio's 'Grabody-T' platform. Uses the PD-L1 arm as tumor-dependent T-cell activator and the 4-1BB arm as conditional T cell activator upon tumor engagement, stimulating 4-1BB activation only in the presence of PD-L1 expressing tumor cells to minimize off-tumor toxicity. In development for solid tumors including non-small cell lung cancer in combination with PD-(L)1 inhibitors. Being jointly developed through a global partnership with ABL Bio.
  • Uliledlimab A differentiated, humanized anti-CD73 monoclonal antibody that targets the CD73 ecto-enzyme which converts extracellular AMP to adenosine in the tumor microenvironment. Features a unique intra-dimer binding mechanism leading to differentiated and favorable functional properties for suppressing tumor growth in combination with checkpoint therapies. Developed for solid tumors with adenosine-driven immunosuppression.

Quantifiable outcome

  • 75% objective response rate and 16.9-month median progression-free survival in Phase 1b givastomig study
  • +2 more outcomes

Companies that use NovaBridge Biosciences

Customer profile

Segments3 records

Ideal customer profiles2 records

NovaBridge Biosciences technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

NovaBridge Biosciences partnerships and signals

Strategic signal

Partnerships

Four partnerships are on record, tiered core, major and minor.

  • ABL BiocoreStrategic or Co-development PartnerABL Bio is a global biotechnology company and key development partner for givastomig (ABL111) and ragistomig (ABL503). Givastomig is being jointly developed through a global partnership with ABL Bio, where NovaBridge is the lead party and shares worldwide rights excluding Greater China and South Korea equally with ABL Bio. Ragistomig (TJ-L14B/ABL503) uses ABL Bio's 'Grabody-T' bispecific antibody platform technology.
  • Everest MedicinesmajorStrategic or Co-development PartnerEverest Medicines holds regional rights to VIS-101 in Greater China and certain Asian territories. Visara (NovaBridge majority-owned subsidiary) grants Everest Medicines exclusive license for development and commercialization of VIS-101 outside NovaBridge's retained territories.
  • ABio-X HoldingsminorStrategic or Co-development PartnerABio-X is shown as a partner logo on NovaBridge's website. Dr. Sean Cao co-founded ABio-X Holdings and serves as director.
  • TJ BiopharmaminorStrategic or Co-development PartnerTJ Biopharma is shown as a partner logo on NovaBridge's website. Chun Kwok Alan Au serves as independent non-executive director of TJ Biopharma since January 2021.

Scale indicators6 records

Recent moves6 records

Expansion highlights6 records

NovaBridge Biosciences competitors and assessment

Company assessment

Direct peers

  • Zymeworks: Clinical-stage biotech with proprietary bispecific antibody platforms (Aziyo and EFECT) used to develop oncology candidates. Highly comparable to NovaBridge's platform-based approach to building a multi-asset bispecific pipeline.
  • Genmab: Industry leader in bispecific antibody technology (Duobody platform) and developer of multiple approved and clinical-stage bispecifics in oncology. Comparable to NovaBridge as a developer of differentiated bispecific antibody therapeutics targeting immuno-oncology indications.
  • Akeso: China-headquartered clinical-stage bispecific antibody developer with multiple oncology assets (e.g., ivonescimab, cadonilimab) and a similar Asia-origin model of advancing innovative biologics globally. Strong overlap with NovaBridge's oncology bispecific strategy and Asian biotech positioning.
  • ABL Bio: South Korea-based clinical-stage biotech developing bispecific antibodies using the Grabody-T platform, which is the same technology underlying NovaBridge's givastomig and ragistomig. ABL Bio is a co-development partner and most directly comparable peer in bispecific antibody design and pipeline.
  • MacroGenics: Clinical-stage oncology biotech developing bispecific antibodies (e.g., DART and TRIDENT platforms) for solid tumors, including PD-L1 x 4-1BB and other immuno-oncology targets that overlap with NovaBridge's ragistomig and givastomig mechanisms.

Broad incumbents

  • Regeneron Pharmaceuticals: Broad biopharmaceutical incumbent and the dominant competitor in retinal vascular disease treatment with Eylea/Eylea HD in the wet AMD/DME market where NovaBridge's VIS-101 will compete. Includes Regeneron to frame VIS-101's competitive landscape.

Regional players

  • Everest Medicines: Asia-region-focused clinical and commercial biopharma with regional rights to NovaBridge's VIS-101 (VEGF-A x ANG-2) for Greater China and selected Asian territories. Operates a similar model of bringing innovative therapeutics into the Asia-Pacific market.

Emerging players

  • Compass Therapeutics: Clinical-stage oncology biotech developing bispecific antibodies (e.g., CTX-009, CTX-112) with checkpoint and tumor-targeted mechanisms comparable to NovaBridge's 4-1BB-based bispecifics. Similar early-stage platform with multiple oncology indications.
  • Cullinan Oncology: Clinical-stage oncology biotech developing multiple targeted therapies (including CLDN18.2 and immuno-oncology assets) with a hub-style pipeline approach similar to NovaBridge's structure. Comparable as a multi-asset oncology biotech.
  • Adagene: Clinical-stage biotech with POWERbody masked antibody platform developing bispecifics and ADCs for oncology, with a comparable China-Asia origin and clinical-stage profile. Overlaps with NovaBridge's approach to engineering differentiated antibody formats.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights7 records

Customer concentration

NovaBridge Biosciences social profiles

Digital presence

NovaBridge Biosciences financial estimates

Financial estimate

Revenue estimate

Valuation estimate

NovaBridge Biosciences leadership team

Management profile

Number of profiles

Profiles15 records

NovaBridge Biosciences subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

NovaBridge Biosciences funding detail

Funding detail

Funding overview

Funding rounds

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

NovaBridge Biosciences M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about NovaBridge Biosciences

What does NovaBridge Biosciences do?

NovaBridge Biosciences is a clinical-stage biopharmaceutical company developing bispecific antibody therapeutics for oncology and ophthalmology indications. The company's pipeline includes givastomig (CLDN18.2 x 4-1BB bispecific antibody) for first-line HER2-negative metastatic gastric cancer, VIS-101 (VEGF-A x ANG-2 bispecific antibody) for retinal vascular diseases, ragistomig (PD-L1 x 4-1BB), and uliledlimab (anti-CD73 mAb). The company operates a Hub-and-Spoke platform linking Asian innovative medicines to global markets, backed by CBC Group.

Is NovaBridge Biosciences a public or private company?

NovaBridge Biosciences is a public company. It is classified as public and is currently operating.

When was NovaBridge Biosciences founded?

NovaBridge Biosciences was founded in 2016. It employs 11 to 50 people.

Where is NovaBridge Biosciences based?

NovaBridge Biosciences is headquartered in Rockville, United States, in the North America region.

How does NovaBridge Biosciences make money?

One revenue line is on record: pharmaceutical Product Revenue.

Who are NovaBridge Biosciences's main competitors?

Direct peers on record are Zymeworks, Genmab, Akeso, ABL Bio and MacroGenics. Regeneron Pharmaceuticals is listed as a broad incumbent. Everest Medicines is listed as a regional player. Emerging players are Compass Therapeutics, Cullinan Oncology and Adagene.

Does NovaBridge Biosciences have an API?

No public API is recorded for NovaBridge Biosciences.

What industry is NovaBridge Biosciences in?

NovaBridge Biosciences's product category is Clinical-Stage Biopharmaceuticals. Its primary akta.pro industry code is HLAAAIAB, Antibody Discovery & Engineering Platforms (display tech, bispecifics, Fc engineering), with a secondary code of HLAAAAAF, Bispecific & Multispecific Antibodies. Its NAICS code is 541714 and its SIC code is 2834.

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Investing.comNovaBridge to present givastomig trial data at ESMO congressNovaBridge Biosciences will present updated Phase 1b trial data for givastomig at ESMO Congress 2026 in Madrid. The study evaluates the Claudin 18.2 x 4-1BB bispecific antibody with nivolumab and chemotherapy in HER2-negative gastroesophageal adenocarcinoma. The FDA has granted Fast Track Designation for the combination.Investing.comNovaBridge to present givastomig trial data at ESMO congressNovaBridge Biosciences will present updated Phase 1b trial data for givastomig at ESMO Congress 2026 in Madrid. The data covers givastomig combined with nivolumab and chemotherapy in HER2-negative, CLDN18.2-positive gastroesophageal adenocarcinoma. The FDA has granted Fast Track Designation for the combination.Stock TitanNovaBridge Biosciences to Present Givastomig at ESMONovaBridge Biosciences will present updated Phase 1b givastomig combination-study results at ESMO Congress 2026 on October 25, 2026. The data covers givastomig, a Claudin 18.2 x 4-1BB bispecific antibody, combined with nivolumab and chemotherapy in HER2-negative gastroesophageal adenocarcinoma. The company plans to advance toward registrational development in first-line metastatic disease.PR NewswireBispecifics Market to Gain Momentum During the Forecast Period (2026-2036) with Expanding Pipeline and Increasing Therapeutic Adoption | DelveInsightThe bispecifics market is expected to grow substantially from 2026 to 2036, driven by rising chronic disease incidence and pipeline launches. The US held the largest 7MM share in 2025, and multiple myeloma is the leading therapeutic area. Emerging therapies like CA-170 and Givastomig are anticipated to reshape the market.YahooNovaBridge Appoints Martin Dewhurst to Board of Directors as an Independent DirectorNovaBridge Biosciences appointed Martin Dewhurst as an independent director and member of its Audit and Compensation Committees, effective immediately. Dewhurst brings over 30 years of healthcare leadership experience, including a decade at McKinsey. The appointment follows the departure of Liu Xin from the board.Stock TitanNovaBridge Appoints Dewhurst as Independent DirectorNovaBridge Biosciences appointed Martin Dewhurst as an independent director and member of its Audit and Compensation Committees, effective immediately. Dewhurst brings over 30 years of healthcare leadership experience, including a decade at McKinsey & Company. The appointment follows the departure of Liu Xin from the board.AdvfnNovaBridge Appoints Martin Dewhurst to Board of Directors as an Independent DirectorNovaBridge Biosciences appointed Martin Dewhurst as an independent director, effective immediately, to its board and audit and compensation committees. He brings over 30 years of healthcare leadership experience, including a decade at McKinsey. The appointment follows the departure of Liu Xin.Investing.comNovaBridge Biosciences EVP Claire Xu disposes of $2,592 of NBP stock By Investing.comNovaBridge Biosciences EVP Claire Xu sold 3,282 shares at $0.79 each on August 31, 2026, for $2,592, after buying 9,382 shares on August 30. The stock is down 56% year-to-date, and the company reported $216 million in cash with no revenue.Stock TitanNovaBridge Biosciences Sets Sept. Investor ConferencesNovaBridge Biosciences (Nasdaq: NBP) announced on August 27, 2026 that its CEO, Srishti Gupta, MD, MPP, will participate in two investor fireside chats in September 2026. The events are the Cantor 2026 Global Healthcare Conference on September 10 and H.C. Wainwright's 28th Annual Global Investment Conference on September 14, both with one-on-one meetings. Webcasts will be available for 90 days.BioSpaceNovaBridge Biosciences to Participate in September 2026 Investor ConferencesNovaBridge Biosciences announced its CEO Srishti Gupta will participate in two investor conferences in September 2026: Cantor on September 10 and H.C. Wainwright on September 14. Both events include fireside chats and one-on-one meetings, with webcasts available for 90 days.