Table 2.
Author | Drug | No. of Patients | Dose | Primary Endpoint | Safety | Associated Therapies | Phase of Study |
---|---|---|---|---|---|---|---|
NCT04206553 [37] |
Dupilumab | 98 (estimated) | Loading dose administered SC, followed by once every 2 weeks (Q2W) | Proportion of patients achieving sustained remission | - | - | Phase 2/3 |
Kaye A. et al., (2018) [38] |
Dupilumab | 1 | 600 mg week 0, 300 mg every other week | Complete remission | NA | No | Case report |
Seyed Jafari S. et al., (2020) [39] |
Dupilumab | 1 | 600 mg week 0, 300 mg every other week | Complete remission | NA | Omalizumab, MFM, TCS | Case report |
Seidman S. et al., (2019) [40] |
Dupilumab | 1 | 600 mg week 0, 300 mg every other week | Improved pruritus, complete remission | NA | PDN, MFM, DXC, nicotinamide, TCS | Case report |
Abdat R. et al., (2020) [41] |
Dupilumab | 13 | 600 mg week 0, 300 mg every other week; 600 mg week 0, 300 mg weekly. 600 mg week 0, 300 mg every 12 days; |
7/13 Disease clearance 5/13 Satisfactory disease control 1/13 No response |
NA | MTX, PDN, IVIg |
Case series |
Zhang Y et al., (2021) [42] |
Dupilumab | 8 | 600 mg week 0, 300 mg every other week | Complete remission (62.5%) | NA | AZA, MPDSN | Comparative Study |
MPDSN = metilprednisolone; MFM = mycophenolate mofetil; MTX = methotrexate; PDN = prednisone; IVIg = intravenous immunoglobulin; AZA = azathioprine; DXC = doxycycline; TCS = topical corticosteroids.