| FDA–Approved Agents |
Doxil® (doxorubicin HCl liposome injection) |
Ortho Biotech |
Reformulated version of doxorubicin; approved in 2007 for use in combination with Velcade in patients who have not received Velcade and have received at least one prior therapy |
Revlimid® (lenalidomide) |
Celgene Corporation |
Immunomodulatory agent with multiple effects; approved in June 2006 for use in combination with dexamethasone in patients who have received at least one prior therapy |
Thalomid® (thalidomide) |
Celgene Corporation |
Immunomodulatory agent with multiple effects; approved in May 2006 for use in combination with dexamethasone as front-line therapy |
Velcade® (bortezomib for Injection) |
Millennium Pharmaceuticals, Inc. |
Proteasome inhibitor initially approved in 2005 for use in patients who have received at least one prior therapy, and in 2008 for front-line therapy |
| Phase III |
Gemzar® (gemcitabine) |
Lilly |
Chemotherapy drug FDA-approved for use in a variety of cancers; being evaluated in combination with other chemotherapy drugs and tandem transplant |
Mozobil® (plerixafor, AMD-3100) |
Genzyme |
Novel agent that enables more rapid and effective mobilization of stem cells in preparation for stem cell transplant |
Tanespimycin (KOS-953; 17-AAG; geldanamycin) |
Bristol-Myers Squibb |
Inhibitor of a heat shock protein (HSP90) that promotes myeloma cell growth and survival and growth; being evaluated in combination with Velcade |
| Phase II |
Actimid™ (pomalidomide, CC-4047) |
Celgene Corporation |
Type of IMiD™ (immunomodulatory drug) being evaluated in combination with dexamethasone |
Aflibercept (VEGF Trap) |
Regeneron/sanofi-aventis |
Anti-angiogenic fusion protein that binds VEGF |
Aplidin® (plitidepsin) |
PharmaMar, SA |
Marine-derived antitumor agent that induces rapid apoptosis |
ATN-224 |
Attenuon |
Small molecule angiogenesis inhibitor being evaluated in combination with Velcade |
Avastin® (bevacizumab) |
Genentech |
Humanized antibody against the VEGF receptor FDA-approved for use in several other cancers; being evaluated as part of several combination therapies |
AVE 1642 |
sanofi-aventis |
Monoclonal antibody directed against insulin growth factor-1 receptor (IGF-1R) being evaluated in combination with Velcade |
Bexxar® (iodine I 131 tositumomab) |
GlaxoSmithKline |
FDA-approved monoclonal antibody that is directed against CD20 and has radioactive iodine 131 attached to it. CD20 is found on B cells and on a small number of myeloma patient's cells during their disease course |
Carfilzomib (PR-171) |
Proteolix |
Novel proteasome inhibitor; also being evaluated in a Phase I trial in combination with Revlimid-dex |
Certican® (everolimus, RAD001) |
Novartis |
mTor inhibitor being evaluated in combination with Nexavar® (sorafenib) |
CNTO 328 |
Centocor |
Anti-interleukin-6 monoclonal antibody being evaluated alone and in combination with Velcade |
Defibrotide |
Gentium SpA (Italy) |
Novel orally bioavailable oligonucleotide with antimyeloma activity and anticoagulant effects |
Denosumab (AMG 162) |
Amgen |
Human monoclonal antibody that targets the receptor activator of nuclear factor kappa B ligand (RANKL) and inhibits bone destruction; being tested in combination with Zometa, as well as in a Phase II study as monotherapy |
Erbitux® (cetuximab) |
BMS/ImClone |
Monoclonal antibody directed against the epidermal growth factor receptor (EGFR) that is FDA approved for use in colorectal and head and neck cancer; being evaluated with dexamethasone |
Mapatumumab (TRM-1, HGS-ETR1) |
Human Genome Sciences |
Monoclonal antibody directed against a specific TRAIL receptor; promotes apoptosis; being evaluated in combination with Velcade |
Nexavar® (sorafenib) |
Bayer/Onxy Pharmaceuticals |
Multi-kinase inhibitor FDA-approved for use in renal cell carcinoma that inhibits cell growth and angiogenesis; being evaluated alone and in combination with other agents |
PD 0332991 |
Pfizer |
Kinase inhibitor being evaluated in combination with Velcade and dexamethasone; represents the first promising cell-cycle based therapy for myeloma |
Perifosine (KRX-0401, D-21266) |
Keryx |
Oral anticancer agent that inhibits cell growth and promotes apoptosis; anti-tumor activity seen in early clinical trials; being evaluated alone and combination with other agents |
Recombinant human mannose-binding lectin (rhMBL) |
Enzon Pharmaceuticals |
Protein therapeutic being developed for the prevention of severe infections in individuals undergoing chemotherapy |
Rituxan® (rituximab) |
Genentech/Biogen Idec |
Monoclonal antibody FDA-approved for use in non-Hodgkin's lymphoma that targets the CD20 marker found on B cells and a small number of myeloma patient's cells during their disease course; being evaluated in combination with other agents, and alone in MGUS and as maintenance therapy |
Romidepsin (depsipeptide, FK228, FR901228) |
Gloucester Pharmaceuticals /Janssen-Cilag Ltd. |
Histone deacetylase (HDAC) inhibitor being evaluated in combination with Velcade-dex |
Sutent® (sunitunib malate, SU11248) |
Pfizer |
Multikinase inhibitor that blocks cancer cell proliferation and angiogenesis; FDA-approved for use in renal cell carcinoma and a type of gastrointestinal cancer |
Thymoglobulin® (rabbit anti-thymocyte globulin (rATG) |
Genzyme |
Agent FDA-approved for use with immunosuppressants in the treatment of acute renal graft rejection; being evaluated in combination with melphalan or Rapamune® (sirolimus) |
Treanda® (bendamustine hydrochloride, SDX-105; known as Ribomustin® in Germany) |
Cephalon Oncology |
Alkylating agent FDA-approved for use in treating chronic lymphocytic leukemia and approved in Germany for use in myeloma; recently evaluated as part of various combination therapies |
Trisenox® (arsenic trioxide, ATO) |
Cephalon |
Anticancer drug FDA-approved for use in acute promyelocytic leukemia |
Vidaza® (azacitidine) |
Pharmion |
Cytotoxic drug FDA-approved for the treatment of myelodysplastic syndromes (MDS) |
Zarnestra™ (R115777, tipifarnib,FTI) |
Ortho Biotech Oncology Research & Development |
Farnesyl transferase inhibitor with evidence of target modulation in phase I trials |
| Phase I |
Anti-KIR (1-7F9) |
Novo Nordisk |
Monoclonal antibody that activates the body's natural killer cells to kill tumor cells |
Elotuzumab (HuLuc63; humanized anti-CS1 monoclonal antibody) |
PDL BioPharma, Inc. |
Monoclonal antibody that binds to CS1, a cell surface protein that is highly expressed on myeloma cells but minimally expressed on normal cells; Being evaluated alone and in combination with Velcade |
GCS-100 |
Prospect Therapeutics |
Carbohydrate-based agent derived from pectin with activity in multiple cancers, and preclinical activity in myeloma |
GRN163L |
Geron Corp. |
Telomerase inhibitor that has been shown in vitro to induce apoptosis and inhibit myeloma cell growth; being evaluated alone and in combination with Velcade |
HCD122 |
Novartis |
Anti-CD40 monoclonal antibody |
HuMax-CD38 |
Genmab |
Human monoclonal antibody that targets the CD38 molecule, which is highly expressed on the surface of myeloma cells |
IMGN901 (huN901-DM1, BB-10901) |
Immunogen |
Monoclonal antibody directed against the CD56 marker found on myeloma cells coupled with a cancer drug |
KW-2478 |
Kyowa Pharmaceutical |
Heat-shock protein 90 (Hsp90) inhibitor |
Masitinib mesylate (AB1010) |
AB Science |
Inhibitor of fibroblast growth factor receptor 3 (FGFR3) that targets a genetic abnormality in myeloma, the t(4;14) translocation; being evaluated in combination with Velcade-dex outside the US |
Milatuzumab (hLL1, IMMU-110) |
Immunomedics |
Humanized monoclonal antibody directed against the CD74 protein found on B cells and myeloma cells |
Oncolytic measles virus (MV-NIS) |
Mayo Clinic |
Genetically engineered measles virus being administered with or without cyclophosphamide |
OPB-31121 |
Otsuka Pharmaceutical Co., Ltd. |
Agent being evaluated in myeloma and non-Hodgkin's lymphoma |
P276-00 |
Nicholas Piramal India Limited |
Cyclin D1 inhibitor |
Panobinostat (LBH589) |
Novartis |
Histone deacetylase (HDAC) inhibitor; induces apoptosis of cancer cells; being evaluated in combination with Velcade and with Revlimid-Dex |
Salinosporamide A (NPI-0052) |
Nereus Pharmaceuticals |
Novel marine derived proteasome inhibitor active against myeloma cells that are resistant to Velcade |
SGN40 |
Seattle Genetics |
Monoclonal antibody directed against CD40 being evaluated in combination with Revlimid-dex or Velcade |
Sprycel® (dasatinib) |
Bristol-Myers Squibb |
Kinase inhibitor FDA-approved for use in chronic myelogenous leukemia; being evaluated in combination with Velcade or Revlimid-dex |
| Torisel™
(temsirolimus, CCI-779)
|
Wyeth |
mTOR inhibitor FDA-approved for use in renal cell carcinoma; being evaluated alone and in combination with Revlimid or Velcade |
Zemplar™ (paricalcitol) |
Abbott |
Activated vitamin D therapy being evaluated in combination with Zometa |
Zevalin® (yttrium Y 90 ibritumomab tiuxetan) |
Cell Therapeutics, Inc. |
Radiolabeled monoclonal antibody FDA-approved for use in combination with Rituxan (rituximab) for the treatment of B-cell non-Hodgkin's lymphoma; the combination is being evaluated prior to high-dose melphalan and stem cell transplant |
Zolinza® (vorinostat, SAHA [suberoylanilide hydroxamic acid]) |
Merck |
Histone deacetylase (HDAC) inhibitor FDA-approved for use in patients with cutaneous T cell lymphoma (CTCL); has shown marked activity preclinically in multiple myeloma and is being evaluated in combination with Velcade or dex |