"We are actually very happy
which the trial results appear in such a prestigious standard medical journal,
thus recognizing the effect chronic wounds have across a number of medical
specialties," commented Bert Slade, MD, FAAAAI, Chief Medical Officer at
Healthpoint Biotherapeutics.
The
Phase 2b trial was created to determine the possible effectiveness of two cell
amounts and a couple of dosing frequencies of HP802-247, when coordinated with
standard care, in comparison with control plus standard care, in healing venous
leg ulcers over a 12-week therapy period. The research was a randomized, double
blind, dose-finding survey involving 228 topics enrolled across 35
investigational centers in the United States.
Overall,
HP802-247 accomplished statistical significance, in contrast with control plus
standard care, in each the primary and secondary endpoints. HP802-247 was usually
well put up within the study with more frequently confirmed adverse events
being skin ulcers, cellulitis, ended infection, and skin irritability. The
security profile as to the active groups was identical to the vehicle control.
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