Biotechnology company Allergy Therapeutics plc (AIM: AGY) on Wednesday reported positive biomarker results from its Phase I/IIa PROTECT trial of VLP Peanut, following the achievement of the study's primary safety endpoint.
The trial demonstrated a consistent immunomodulatory response in peanut-allergic subjects, with increasing doses of VLP Peanut linked to significant reductions in basophil sensitivity to peanut and Ara h2 versus baseline. At the highest dose, reductions reached 376% for peanut and 489% for Ara h2 compared with placebo, both achieving statistical significance.
Further biomarker analysis showed a statistically significant, dose-dependent decrease in Ara h2 binding to effector B-cells, alongside a clear increase in Ara h2-specific IgG levels across dose groups. Skin prick testing also indicated an absolute reduction in wheal diameter one month post-treatment, contrasting with a slight increase in the placebo group.
The PROTECT trial completed final dosing in December 2025 and evaluated safety, tolerability and preliminary efficacy of the short-course immunotherapy candidate. No significant safety concerns were identified despite a 2,000-fold dose escalation.
Allergy Therapeutics said the results support progression towards a Phase IIb trial, with dose selection informed by the combined safety and efficacy data.
ALK partners with GenSci to expand allergy immunotherapy market in China
Ionis publishes positive Phase 3 data supporting donidalorsen as HAE prophylactic
Blacksmith Medicines granted US patent for antibacterial compounds targeting LpxC
Alvotech reports positive topline results for Xolair biosimilar study
DBV Technologies secures up to USD306.9m to advance Viaskin peanut patch programme
Celltrion's OMLYCLO receives US FDA approval
Kenox Pharmaceuticals partners with Lactiga US
Health Canada approves ALK's ACARIZAX for young children with dust mite allergy
Allergy Therapeutics publishes positive Phase III data for Grass MATA MPL
CSL's ANDEMBRY receives European approval to prevent attacks of hereditary angioedema
NICE recommends ALK's ACARIZAX for house dust mite allergic rhinitis treatment in UK's NHS
European Commission approves Palforzia for toddlers with peanut allergy
Eli Lilly and Co receives approval from FDA for Zepbound
CSL gains EMA backing for Garadacimab as HAE prophylactic treatment