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Helix BioPharma Corp Announces Phase II Clinical Trial Results of Topical Interferon Alpha-2b in Patients With Ano-Genital Warts

Helix BioPharma Corp Announces Phase II Clinical Trial Results of Topical Interferon Alpha-2b in ...

articleHelix Biopharma Corp.June 8, 20103/company/helix-biopharma-corp/news/helix-biopharma-corp-announces-phase-ii-clinical-trial-results-of-topical-interferon-alpha-2b-in-patients-with-ano-genital-warts
Helix BioPharma Corp Announces Phase II Clinical Trial Results of Topical Interferon Alpha-2b in Patients With Ano-Genital Warts

About this update from Helix Biopharma Corp.

[{"type":"text","content":"\n\n\n\n Jun. 8, 2010 (Canada NewsWire Group) -- \n >\n\n Helix BioPharma Corp. (TSX, FSE: "HBP" / OTCQX: HXBPF) today announced results from the Phase II clinical trial assessing the efficacy and safety of Topical Interferon Alpha-2b cream for the treatment of ano-genital warts (AGW).\n\nAnalysis of the primary study endpoint, that is, the proportion of patients with complete clearance of their baseline lesions during the eight week treatment period, as well as the secondary efficacy endpoints, showed no statistically significant treatment effects between the treatment and the placebo groups. Topical Interferon Alpha-2b was very well tolerated. Local skin reactions (e.g., itching, burning or pain) in both groups were mostly absent or mild, and there were no treatment-related serious adverse events, which is consistent with previous clinical findings with Topical Interferon Alpha-2b.\n\n"We remain focused on our lead indication, the treatment of women with low grade cervical lesions, based on our previously announced positive Phase II study results for this indication," said John Docherty, president and COO of Helix BioPharma. "Despite the lack of efficacy shown for the AGW indication, we are pleased with this trial's tolerability results which strengthen our safety database for future clinical testing. We are on track to file our IND for our planned Phase II/III trial in the U.S. for our lead indication in or around the end of fiscal 2010, subject to successful completion of our remaining IND-enabling activities as previously reported. We will be considering the results of the AGW study in detail to determine our next steps forward for this indication, if applicable."\n\n >\n\nHelix BioPharma Corp. is a biopharmaceutical company focused on cancer therapy. The Company is actively developing innovative products for the prevention and treatment of cancer based on its proprietary technologies. Helix's product development initiatives include its Topical Interferon Alpha- 2b and its novel L-DOS47 new drug candidate. Helix is listed on the TSX under the symbol "HBP". For more information, please visit www.helixbiopharma.com.\n\n\n\nFor further information contact:\n\n\n >\n\nThis News Release contains forward-looking statements and forward-looking information (collectively, "forward-looking...

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