Objectives: This study aimed to evaluate the effi cacy of Rituximab in the management of idiopathic membranous nephropathy (IMN) based on the following criteria: (I) Biological remission at three months (M3) and six months (M6); (II) change in mean proteinuria (24PU), mean serum albumin, and mean serum creatinine at M3 and M6; (III) and side eff ects. Methods: This retrospective descriptive and analytical study included patients with histologically confi rmed IMN with positive plasma anti-PLA2R antibodies who received at least one dose of Rituximab after six months of follow-up without spontaneous remission. Patients with unexplainable records were not included. Results: A total of fi ve patients (P1, P2, P3, P4, and P5), including four males and one female were analyzed. The mean age was 44. 20 23. 14 years. All patients had IMN type 2. At inclusion, the mean albuminemia, mean creatinine, and mean 24hPU levels were 15. 56 5. 27 g/L, 17. 3 7. 6 mg/L, and 6. 54 1. 13 g/24h, respectively. The median anti-PLA2R antibody titer was 100 IU with extremes of 10 and 800 IU. Partial remission was noted in three patients at M3 (P2, P4, and P5), and it was maintained until M6 in P2. No complete remission was observed. A signifi cant decrease in mean 24hPU at M3 was noted (P < 0. 001). Generalized pruritus associated with seizures was noticed in P4 after the fi rst dose of Rituximab. Conclusions: Partial remission was noted in three patients at M3, and one patient maintained this remission at M6. Rituximab signifi cantly reduced 24hPU at M3 after administration. Rituximab administration was well tolerated by the patients.