Moberg Pharma reports topline data in the North American phase 3 study and will regain rights to MOB-015 in EU
Moberg Pharma AB (OMX: MOB) announces that MOB-015 (topical terbinafine) did not meet the primary endpoint in the phase 3 study using 8 weeks of daily dosing followed by weekly maintenance dosing. The company’s focus going forward will be on the effective daily dosing regimen approved in 13 EU countries.In line with previous communication on September 13[th ]2024, the results now confirm that the primary endpoint was not met. The North American Phase 3 study was conducted at 33 study centers in the US and Canada, including a total of 384 patients, 260 patients receiving MOB-015 and 124