US-based clinical-stage biotechnology company HDT Bio Corp announced on Sunday the establishment of HDT Bio Canada Inc, its Canadian subsidiary, formed to advance its cancer immunotherapy programs through Canadian clinical development, Canadian manufacturing, and Canadian regulatory pathways.
The company has partnered with McGill University and The Neuro (Montreal Neurological Institute-Hospital) for the clinical development of HDT-401, its investigational locally administered immune activator for glioblastoma.
HDT-401 has already been administered to glioblastoma patients under compassionate use protocols. According to the company, the results were encouraging enough to inform and shape the design of a formal Phase 1 clinical trial. HDT Bio Canada has completed a pre-Clinical Trial Application meeting with Health Canada, a required regulatory step on the path to trial initiation, and has received constructive feedback that advances the programme toward CTA submission.
HDT-401 combines Riboxxim, a precisely engineered molecule licensed from Riboxx GmbH of Dresden, Germany, with HDT Bio's proprietary LION nucleic acid delivery platform. It is designed to activate innate immune sensing directly within the tumour bed, converting the glioblastoma microenvironment from immune-suppressed to immune-engaged. The approach is intended to induce inflammatory cytokines, recruit immune effector cells, and support local immune recognition of tumour tissue. Local administration into the tumour or surgical cavity concentrates immune activation at the site of disease while limiting systemic exposure.
Vascarta announces VAS-101 Phase I results in sickle cell disease patients
Cirius Therapeutics commences enrolment and dosing for Phase 2 study of CIR-0602K in type 1 diabetes
Kither Biotech completes Phase 1 KIT2014 clinical study
Gesynta Pharma reports progress in Phase 2 trial of vipoglanstat
Hillhurst Bio reports first subject dosed in Phase 2a trial of HBI-002 for Parkinson's disease
Organon secures FDA approval expanding TOFIDENCE indications for CRS and paediatric COVID-19
Sanofi halts phase 3 MOBILIZE study of riliprubart in CIDP
Lynk Pharmaceuticals' partner Formation Bio doses first participant in BLKR201 Phase 1 trial
FDA grants rare paediatric disease designation to RedHill's opaganib
Antengene presents first ATG-207 preclinical data at EULAR 2026
Gilead and Lakefront complete Ouro Medicines acquisition to expand autoimmune disease pipeline
Breckenridge launches Tofacitinib Tablets, generic equivalent to Pfizer's Xeljanz
UCB launches scholarship program for adults living with hidradenitis suppurativa