Phathom’s Voquezna Triple PAK & Voquezna Dual PAK Receives the US FDA’s Approval for the Treatment of H. pylori Infection in Adults
Shots:
- The approvals were based on P-III (PHALCON-HP) trial evaluating Voquezna Triple & Dual PAK vs lansoprazole triple therapy in 1046 patients with H. pylori inf. The therapies are expected to be available in the US in Q3’22
- The results from both Voquezna treatment regimens showed non-inferiority over lansoprazole triple therapy in patients without a CAM or AMX resistant strain of H. pylori at baseline in modified ITT population, eradication rate (84.7% & 78.5% vs 78.8% & 78.8%), superior eradication rates over PPI-based triple therapy in patients with CAM resistant strains of H. pylori
- In the overall study population, eradication rate (80.8% & 77.2% vs 68.5% & 68.5%) who had a CAM-resistant strain of H. pylori (65.8% & 69.6% vs 31.9%, & 31.9%), respectively
Ref:Globe Newswire | Image: Phathom Pharmaceuticals
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