DNB Carnegie Nordic Healthcare Conference presentation
Logotype for Nykode Therapeutics

Nykode Therapeutics (NYKD) DNB Carnegie Nordic Healthcare Conference presentation summary

Event summary combining transcript, slides, and related documents.

Logotype for Nykode Therapeutics

DNB Carnegie Nordic Healthcare Conference presentation summary

15 May, 2026

Strategic focus and clinical pipeline

  • Advancing three core programs: Abi-suva for HPV16+ cancers, VB10.NEO for individualized neoantigen therapy, and an Antigen-Specific Immune Tolerance (ASIT) platform for autoimmune diseases.

  • Abi-suva demonstrates strong and durable clinical responses in multiple trials, with a phase 2 RCT in 1L r/m head and neck cancer targeting interim data within 24 months.

  • VB10.NEO leverages robust immune responses and a proprietary AI algorithm for neoantigen selection, with rapid 7-week manufacturing turnaround and cost advantages over mRNA approaches.

  • ASIT platform aims to transform autoimmune disease treatment by inducing durable, disease-specific immune tolerance, supported by promising preclinical data.

  • Disciplined cost management ensures a cash runway into 2028-2029, supporting key program milestones.

Clinical data and market opportunity

  • Abi-suva plus atezolizumab shows a 29% ORR and 24.7 months median overall survival in 2L+ cervical cancer, outperforming CPI monotherapy.

  • HPV16+ HNSCC market projected to grow from $1.1bn in 2025 to $2.3bn in 2034, with significant unmet need for HPV-positive specific treatments.

  • Abili-T trial in 1L HNSCC is enrolling up to 100 patients, with interim efficacy analysis expected in 2027.

  • VB10.NEO positioned as a leading unencumbered INT, with peer readouts in the next 15 months expected to validate the approach.

Technology and platform differentiation

  • Proprietary APC-targeting technology enables precise modulation of immune responses for oncology and autoimmune indications.

  • pDNA-based manufacturing for VB10.NEO offers faster, less complex, and lower-cost production compared to mRNA.

  • ASIT platform demonstrates efficacy in preclinical EAE models, reducing effector T cells, increasing regulatory T cells, and lowering auto-antibody levels.

  • Technology supports convenient delivery routes, including intravenous and subcutaneous administration.

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