Clinical Hold Removed For Helix Biopharma Corp.'s Topical Interferon Alpha-2B Phase II/III Efficacy Trial IND Application
11/14/2011
Helix BioPharma Corp. (TSX, NYSE Amex, FSE: “HBP”), a biopharmaceutical
company developing drug candidates for the prevention and treatment of cancer, today announced that the “clinical hold” on
its investigational new drug (“IND”) application for its Topical Interferon Alpha-2b, Phase II/III, low-grade cervical lesion
efficacy trial has been removed by the United States Food and Drug Administration (“FDA”).