TWO:4168 · Clinical-Stage Biotech · Taipei

GlycoNex: Pioneering Glycan-Directed Cancer Immunotherapy

20 years of glycobiology. Validated by Japan's PMDA in 2026. Ready for global partnership.

5
Active programs
in clinical and preclinical development
20+
Years of dedicated
glycobiology research
200L
In-house GMP
manufacturing capacity
Our Business

Three Core Business Areas

Innovative Drug

GlycoNex's core capability is discovering antibodies against tumor-associated carbohydrate antigens. These anti-glycan antibodies anchor a pipeline of ADCs, pro-antibody ADCs, and bispecific ADCs — led by GNX1021, now in Phase 1.

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Service (CDMO)

Contract development and manufacturing from a 50 L + 200 L GMP antibody facility: cell-line development, upstream and downstream process development, scale-up, and technology transfer for external partners.

CDMO services →

Biosimilar

Two biosimilar programs: SPD8 (denosumab biosimilar, Phase 3 complete), co-developed with Mitsubishi Gas Chemical; and SSR, a biosimilar for an autoimmune disease, developed in-house.

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Clinical Pipeline

From bench to bedside

Drug Code
Class
Indication
Phase
Next milestone
GNX1021
Anti-Glycan ADC
GI cancers (gastric, CRC, pancreatic)
Japan first patient: Jun 2026
SPD8
Biosimilar
Osteoporosis
Topline data: Q2 2026
GNX201-ADC
Pro-Antibody ADC
Confidential
Lead optimization
GNX203
Bispecific ADC
Pancreatic, colorectal, gynecologic
Lead optimization
Technology

Built on Two Decades of Glycobiology

GlycoSH Antibody Bank

One of the most extensive collections of anti-glycan monoclonal antibodies — over 50 to date — accumulated through two decades of dedicated research.

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Glycan-Directed ADCs

Antibody-drug conjugates that pair GlycoNex's anti-glycan antibodies with clinically validated linker technology, directed at tumor-associated carbohydrate antigens that distinguish malignant from healthy cells.

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200L GMP Manufacturing

In-house GMP-compliant antibody production for Phase 1 clinical supply and external CDMO partners.

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Latest Updates

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Regulatory

GNX1021 Cleared by Japan PMDA for Phase 1 Clinical Trial

Japan's Pharmaceuticals and Medical Devices Agency has authorized first-in-human dosing for GlycoNex's lead glycan-targeted ADC in patients with refractory GI cancers.

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Partnership

GlycoNex Partners with Nippon Kayaku on GNX201-ADC

Strategic preclinical collaboration on a next-generation pro-antibody ADC, with Nippon Kayaku contributing payload chemistry expertise.

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Pipeline

Second Biosimilar Program Initiated for Immunology Indications

Building on SPD8 manufacturing experience, GlycoNex extends its biosimilar portfolio toward a high-volume immunology target.

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Clinical

SPD8 Phase 3 Enrollment Completed

All patients enrolled in the Japan Phase 3 trial; topline efficacy and safety readout anticipated in Q2 2026.

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Network

Trusted by Global Partners

And presented at

Looking for a partner in glycan-targeted oncology?

GlycoNex is actively seeking global licensing and co-development partners across our Phase 1+ pipeline.

Get in Touch →