Overview Efficacy/ Safety of Product DNN.65.21.005 in Patients With Benign Prostatic Hyperplasia Status: NOT_YET_RECRUITING Trial end date: 2027-04-01 Target enrollment: Participant gender: Summary To evaluate the safety and efficacy of DNN.65.21.005 versus Combodart in the treatment of benign prostatic hyperplasiaPhase: PHASE3 Details Lead Sponsor: Ache Laboratorios Farmaceuticos S.A.