Forbius, a clinical-stage company that develops novel biologics for the treatment of cancer and fibrosis, has revealed that it has dosed its first patient in a Phase 2a triple negative breast cancer (TNBC) clinical trial with AVID100, a novel, tumour-specific anti-epidermal growth factor receptor (EGR) antibody-drug conjugate (ADC), it was reported yesterday.
The multicentre, dose-expansion, Phase 2a trial (AVID100-01; NCT03094169) will assess the efficacy, safety, and tolerability of AVID100 in patients with advanced, EGFR-overexpressing, TNBC (IHC 2+/3+). This is the third cohort launched and follows the earlier announced cohorts assessing AVID100 in patients with advanced squamous non-small cell lung cancer (sqNSCLC) and squamous cell carcinoma of the head and neck (SCCHN). In total, around 100 patients will be assessed across three EGFR-overexpressing tumour types: sqNSCLC, SCCHN, and TNBC.
AVID100 is a highly potent EGFR-targeting antibody-drug conjugate designed to achieve improved anti-tumour efficacy without a corresponding increase in toxicity against skin and other EGFR-expressing normal tissues. In preclinical studies, the product indicated significant anti-cancer activity in EGFR-overexpressing tumour models resistant to marketed EGFR inhibitors. AVID100 is the most advanced, broadly active anti-EGFR ADC in clinical development and targets both wild-type and mutant forms of EGFR.
Norgine submits first marketing authorisation application submissions for approval of eflornithine
Innovent Biologics names new Oncology CMO
UroGen's UGN-103 IND accepted by FDA for bladder cancer treatment
Innate Pharma advances Sanofi-developed NK cell engager to Phase 2 for blood cancer patients
Portage Biotech expands evaluation of strategic alternatives
Stamford Pharmaceuticals starts locally advanced basal cell carcinoma (laBCC) trial of SP-002
QST selects RayStation for advanced carbon ion therapy
Candel Therapeutics granted FDA Orphan Drug Designation for CAN-2409 in pancreatic cancer treatment
Innate Pharma reports preclinical efficacy of IPH45
Roche attains CE Mark for first companion diagnostic for HER2-low metastatic breast cancer
BioCity Biopharma's BC2027 Phase one study IND application receives US FDA approval
enGene Holdings names new senior vice president, Urologic Oncology and Clinical Development
CLS secures second order from NIH Clinical Center for Thermal Therapy System accessories