Peptide News Digest

#Biomarker

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Clinical Trials · View digest

Eisai Presents Anti-MTBR Antibody Etalanetug (E2814) Plasma Biomarker Data at AAIC 2026 Featured Research Session: Etalanetug Reduced Plasma MTBR-Tau243 by 78% at 3 Months and by More Than 90% at 9 Months, With the Biomarker Largely Absent in Healthy Adults and Detected Only in Patients With Dominantly Inherited Alzheimer's Disease (DIAD), Reflecting Disease-Related Tau Neurofibrillary Tangle Pathology That Blood-Test Monitoring Can Now Track

Eisai announced Monday July 13, 2026 that its investigational anti-microtubule-binding region (MTBR) tau antibody etalanetug (development code E2814) reduced levels of plasma extracellular MTBR-tau243 (eMTBR-tau243), a novel fluid biomarker of Alzheimer's disease tau tangle pathology, in findings presented during a Featured Research Session at AAIC 2026 in London. Etalanetug reduced plasma eMTBR-tau243 by 78% at 3 months and by more than 90% at 9 months. The biomarker was largely absent in healthy adults and detected only in patients with dominantly inherited Alzheimer's disease (DIAD), suggesting it reflects disease-related tau pathology at the pathological source (neurofibrillary tangle formation) rather than tau physiology broadly. eMTBR-tau243 consists of tau fragments that include amino acid residue 243 and MTBR sequences, arising during the formation of neurofibrillary tangles, and can now be measured with a blood test to track tau pathology non-invasively. Etalanetug is Eisai's second-generation Alzheimer's antibody program beyond lecanemab (LEQEMBI, amyloid protofibril-directed), extending the company's franchise from amyloid to tau.

Clinical Trials · View digest

BriaCell Bria-IMT ASCO 2026 Biomarker Detail: 65% of Heavily Pretreated Breast Cancer Patients Showed CAML Stability/Drop Correlating With Better Progression-Free Survival

BriaCell's ASCO 2026 poster presentations added a biomarker finding beyond the headline 16.6-month median overall survival for Bria-IMT. In an ongoing analysis of heavily pretreated metastatic breast cancer patients, 65% showed stability or a drop in Cancer-Associated Macrophage-Like cells (CAMLs) — circulating cells in the blood that reflect tumor activity — and that change significantly correlated with better progression-free survival. The CAML biomarker offers a potential early blood-based readout of Bria-IMT response, which matters for an immunotherapy where conventional imaging can lag the immune response. BriaCell's six ASCO 2026 data items (three posters, three publication-only abstracts) cover the pivotal Phase 3 Bria-ABC study of Bria-IMT plus checkpoint inhibitor plus further Phase 2 analyses. Bria-IMT is a whole-cell allogeneic peptide-and-cell immunotherapy in heavily pretreated metastatic breast cancer that has failed ADC, checkpoint, and CDK4/6 inhibitor therapy. The biomarker work supports patient selection and response monitoring as the program advances toward accelerated-approval discussions.