Peptide News Digest

#Functional-Cure

2 stories

Clinical Trials · View digest

EASL 2026 Closing-Day HBV Functional-Cure Late-Breakers: TUNE-401 Epigenetic Silencer, Precision PBGENE-HBV cccDNA Elimination, Brii Bio BRII-179 Therapeutic Vaccine ENSURE

EASL 2026's final day delivered a cluster of hepatitis B functional-cure late-breakers spanning gene, epigenetic, and immune approaches. TUNE Therapeutics presented TUNE-401 (May 30, 13:30 CEST), a first-in-class epigenetic silencer of HBV demonstrating deep and durable antiviral activity. Precision BioSciences presented PBGENE-HBV gene-editing data from the ELIMINATE-B study showing first evidence of elimination and inactivation of cccDNA — the persistent viral reservoir that makes HBV functionally incurable — in liver biopsies from treated chronic HBV patients. Brii Bio presented end-of-study data from the Phase 2 ENSURE study supporting BRII-179, a protein-based therapeutic HBV vaccine designed to restore immune control. The functional-cure wave advances alongside the entry-inhibitor approaches covered earlier in the week — Gilead's just-approved bulevirtide peptide (Hepcludex) and Assembly Biosciences' oral ABI-6250 — illustrating that HBV/HDV is becoming a multi-modality battleground across peptides, gene editing, epigenetic silencing, and therapeutic vaccines.

Clinical Trials · View digest

Aligos Therapeutics EASL 2026 HBV Combination Data: ALG-170675 ASO Synergizes With Pevifoscorvir Sodium; 40% of HBeAg+ Patients Reach HBsAg Levels Qualifying for ASO Therapy at Week 48

Aligos Therapeutics presented additional EASL 2026 data on its chronic hepatitis B (HBV) combination strategy. An analog of ALG-170675, a potential best-in-class antisense oligonucleotide (ASO), demonstrated additive-to-synergistic effects when combined with ALG-001075 (the active parent moiety of pevifoscorvir sodium, a capsid assembly modulator). Separately, 40% of HBeAg-positive chronic HBV patients treated with pevifoscorvir sodium for 48 weeks reached HBsAg reductions low enough to potentially qualify for ASO treatment — supporting a sequencing strategy toward functional HBV cure where the capsid modulator lowers viral antigen load before the ASO finishes the job. The data complements the ALG-055009 THR-β MASH results (46.2% liver-fat reduction) Aligos presented earlier in the week. The combination-and-sequencing approach mirrors the broader trend in liver disease toward layered mechanisms rather than single-agent therapy, and positions Aligos across the HBV, HDV, and MASH liver-disease franchises.