Humacyte reports Q4 EPS (4c), consensus (23c)

Reports Q4 revenue $0, consensus $200,000. "During 2022, we continued to make significant progress across all of our clinical programs and are poised to maintain this momentum throughout 2023," said Laura Niklason, M.D., Ph.D., Chief Executive Officer of Humacyte. "With enrollment approaching completion in our Phase 2/3 trial of the HAV in its vascular trauma indication, we have moved substantially closer to our anticipated filing of a Biologics License Application in this indication. The potential of the HAV in vascular trauma was highlighted in a compelling key opinion webinar we hosted in December, featuring Ukrainian surgeons Drs. Oleksandr Sokolov, Vasyl Shaprynskyi, and Oleksandr Stanko. We extend our sincere thanks to our Ukrainian colleagues for sharing their experiences using the HAV to treat patients with wartime vascular trauma. In addition to our vascular trauma indication, we are excited to be nearing completion of enrollment in our Phase 3 trial of the HAV in arteriovenous access for hemodialysis patients, with topline results anticipated one year following completion of enrollment. Finally, we continue to be encouraged with the preclinical progress of our small diameter HAV in coronary artery bypass grafting, which we believe further supports the utility of our HAV as a vascular conduit across multiple indications."