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©2013 Baishideng Publishing Group Co.
World J Transplant. Dec 24, 2013; 3(4): 68-77
Published online Dec 24, 2013. doi: 10.5500/wjt.v3.i4.68
Published online Dec 24, 2013. doi: 10.5500/wjt.v3.i4.68
Generic | Brand | FDA indication | Company |
Alefacept12 | Amevive | Treatment of moderate-to-severe chronic plaque psoriasis in adults who are candidates for systemic therapy or phototherapy | Astellas |
Alemtuzumab2 | Campath | Treatment of B-CLL | Berlex Laboratories |
ASKP1240 | Not FDA approved | Astellas | |
Azathioprine | Imuran | Adjunctive therapy in prevention of rejection of kidney transplants; management of active rheumatoid arthritis | Generic manufacturers |
Basiliximab | Simulect | Prevention of acute rejection in kidney transplantation | Novartis |
Belatacept | Nulojix | Prevention of acute rejection in renal transplant recipients | Bristol-Myers-Squibb |
Bortezomib | Velcade | Treatment of multiple myeloma; treatment of relapsed or refractory mantle cell lymphoma | Millenium Pharmaceuticals |
Cyclosporine | Neoral | Prevention of acute rejection in renal transplant recipients | Novartis |
Eculizumab | Soliris | Treatment of PNH to reduce hemolysis and aHUS | Alexion Pharmaceuticals |
Efalizumab12 | Raptiva | Management of moderate to severe chronic plaque psoriasis in adults | Genentech |
Everolimus | Afinitor, Zortress | Treatment of advanced renal cell cancer (Afinitor®); treatment of subependymal giant cell astrocytom associated with tuberous sclerosis (Afinitor®); treatment of advanced, metastatic or unresectable pancreatic neuroendocrine tumors (Afinitor®); prophylaxis of organ rejection in patients at low-moderate immunologic risk receiving renal transplants (Zortress®) | Novartis |
Mycophenolate Mofetil | Cellcept | Prophylaxis of organ rejection concomitantly with cyclosporine and corticosteroids in patients receiving allogeneic renal cardiac, or hepatic transplants | Genentech |
Mycophenolate Sodium | Myfortic | Prophylaxis of organ rejection concomitantly with cyclosporine and corticosteroids in patients receiving allogeneic renal transplantation | Novartis |
Horse or Rabbit anti-thymocyte Globulin | Atgam or Thymoglobulin | Treatment of corticosteroid resistant rejection in kidney transplantation | Pfizer/Sanofi |
Rituximab | Rituxan | Treatment of CD20-positive non-Hodgkin’s lymphomas ; Treatment of moderately- to severely-active rheumatoid arthritis in adult patients with inadequate response to one or more TNF antagonists; Treatment of Wegener’s granulomatosis; Treatment of microscopic polyangiitis | Genentech |
Sirolimus | Rapamune | Prevention of acute rejection in renal transplant recipients | Pfizer |
Sotrastaurin, AEB-0711 | Not FDA approved | Novartis | |
Tacrolimus | Prograf | Prevention of acute rejection in renal transplant recipients | Astellas |
Tacrolimus Prolonged Release | Astragraf XL | Preventing organ rejection in kidney transplant recipients, as combination therapy with mycophenolate mofetil and corticosteroids, with or without tasiliximab induction | Astellas |
Tolfacitinib1 | Xeljanz | Treatment of moderate to severe rheumatoid arthritis | Pfizer |
Voclosporin | Not FDA approved | Isotechnika Pharma |
Drug name | Mechanism of action |
Induction | |
Efalizumab1 | Humanized antibody, CD11a/LFA-1 |
Alefacept1 | Costimulation inhibitor, CD2 LFA3 |
Maintenance | |
Voclosporin, ISA247 | Calcineurin inhibitor |
Sotrastaurin, AEB0711 | Protein kinase C inhibitor |
Tofacitinib, CP-6905501 | JAK 3 inhibitor |
ASKP1240 | Anti-CD40 monoclonal antibody |
Treatment of Antibody Medicated Rejection | |
Bortezomib | Proteasome inhibitor |
Eculizumab | Monoclonal antibody, C5 complement protein |
Agent | Identifier | Study name | Start date |
ASKP1240 | NCT01780844 | A Study to Assess the Efficacy and Safety of ASKP1240 in de Novo Kidney Transplant Recipients | February 2013 |
Voclosporin | NCT01586845 | Safety and Efficacy Study of Voclosporin and Tacrolimus in Transplantation | March 2013 |
Prolonged Release Tacrolimus | NCT01294020 | Study to Compare the Pharmacokinetics of Tacrolimus in Stable Pediatric Allograft Recipients Converted From Prograf® to Advagraf® | May 2011 |
Bortezomib | NCT01873157 | Bortezomib in Late Antibody-mediated Kidney Transplant Rejection (BORTEJECT) | October 2013 |
NCT01349595 | Impact of Proteasome Inhibition on Anti-Donor HLA Antibody Production After Kidney Transplantation | December 2011 | |
NCT01842074 | Desensitization With Bortezomib Before a Living Kidney Donation (VELDON) | January 2013 | |
NCT01502267 | Desensitization Protocol for Highly Sensitized Patients on the Waiting List for Kidney Transplant | January 2010 | |
NCT00722722 | The Impact of Velcade on Antibody Secreting Cells in Sensitized Renal Allograft Candidates | June 2008 | |
Eculizumab | NCT01349595 | Impact of Proteasome Inhibition on Anti-Donor HLA Antibody Production After Kidney Transplantation | December 2011 |
NCT01327573 | Eculizumab Therapy for Chronic Complement-Mediated Injury in Kidney Transplantation | March 2011 | |
NCT01095887 | Eculizumab Added to Conventional Treatment in the Prevention of Antibody-mediated Rejection in ABO Blood Group Incompatible Living Donor Kidney Transplantation (ABOi) | March 2010 | |
NCT01403389 | A Study of the Activity of Eculizumab for Prevention of Delayed Graft Function In Deceased Donor Kidney Transplant | August 2011 | |
NCT01567085 | Safety and Efficacy Of Eculizumab In The Prevention Of Antibody Mediated Rejection (AMR) In Sensitized Recipients Of A Kidney Transplant From A Deceased Donor | May 2012 | |
NCT01106027 | Dosing Regimen of Eculizumab Added to Conventional Treatment in Positive Crossmatch Deceased Donor Kidney Transplant | March 2010 | |
NCT01399593 | Safety and Efficacy of Eculizumab to Prevent AMR in Living Donor Kidney Transplant Recipients Requiring Desensitization | September 2011 |
- Citation: Hardinger KL, Brennan DC. Novel immunosuppressive agents in kidney transplantation. World J Transplant 2013; 3(4): 68-77
- URL: https://www.wjgnet.com/2220-3230/full/v3/i4/68.htm
- DOI: https://dx.doi.org/10.5500/wjt.v3.i4.68