Helix BioPharma Corp. (TSX, FSE: "HBP") announced today that it has initiated patient enrollment in a Phase II clinical trial of Topical Interferon Alpha-2b for the treatment of ano-genital warts (condylomata accuminata) associated with human papilloma virus ("HPV") infection.
The trial, which is taking place in Sweden, will assess the efficacy and safety of Topical Interferon Alpha-2b compared with placebo using a double blind, randomized design over an examination period of four months per patient. One hundred twenty patients are to be enrolled in the trial. Half will receive a placebo and half will receive Topical Interferon Alpha-2b receiving
The trial, which is taking place in Sweden, will assess the efficacy and safety of Topical Interferon Alpha-2b compared with placebo using a double blind, randomized design over an examination period of four months per patient. One hundred twenty patients are to be enrolled in the trial. Half will receive a placebo and half will receive Topical Interferon Alpha-2b receiving
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