ertumaxomab
Ertumaxomab is a rat-murine hybrid monoclonal antibody designed to treat some types of cancer. — Wikipedia
Clinical trial activity
4 trials · 5 clinical orgs · 0 marketing orgs
Earliest trial started Jul 1, 2006 (NCT00351858)
Timeline
Indications
Mechanism of action
CD3E activator
Immunomodulator. Trifunctional bispecific monoclonal antibody (mAb) has the capacity to enhance immunological effector functions such as antibody dependent cell-mediated cytotoxicity (ADCC) and antibody-dependent cellular phagocytosis (ADCP). Designed to induce the formation of tri-cell-complexes consisting of Her2-positive tumor cells, CD3+ T cells, and Fc¿-receptor positive accessory cells.
- Receptor protein-tyrosine kinase erbB-2BINDING AGENT
ERBB2 binding agent
Immunomodulator. Trifunctional bispecific monoclonal antibody (mAb) has the capacity to enhance immunological effector functions such as antibody dependent cell-mediated cytotoxicity (ADCC) and antibody-dependent cellular phagocytosis (ADCP). Designed to induce the formation of tri-cell-complexes consisting of Her2-positive tumor cells, CD3+ T cells, and Fc¿-receptor positive accessory cells.
- T-cell surface glycoprotein CD3 epsilon chainCROSS-LINKING AGENT
T-cell surface glycoprotein CD3 epsilon chain cross-linking agent
Immunomodulator. Trifunctional bispecific monoclonal antibody (mAb) has the capacity to enhance immunological effector functions such as antibody dependent cell-mediated cytotoxicity (ADCC) and antibody-dependent cellular phagocytosis (ADCP). Designed to induce the formation of tri-cell-complexes consisting of Her2-positive tumor cells, CD3+ T cells, and Fcγ-receptor positive accessory cells.
- Receptor protein-tyrosine kinase erbB-2CROSS-LINKING AGENT
Receptor protein-tyrosine kinase erbB-2 cross-linking agent
Immunomodulator. Trifunctional bispecific monoclonal antibody (mAb) has the capacity to enhance immunological effector functions such as antibody dependent cell-mediated cytotoxicity (ADCC) and antibody-dependent cellular phagocytosis (ADCP). Designed to induce the formation of tri-cell-complexes consisting of Her2-positive tumor cells, CD3+ T cells, and Fcγ-receptor positive accessory cells.
Chemistry & pharmacology
- Chirality
- Single Stereoisomer
- Inorganic
- No
- Polymer
- No
- Multi-specific
- Yes
Oral
No
Parenteral
No
Topical
No
Sources
- WikipediaErtumaxomab ↗
- ChEMBLCHEMBL2108029 ↗
Also known as
- ertumaxomab
- ertumaxomab
- rexomun
Clinical trials
| NCT ID | Phase | Start date | Sponsor(s) |
|---|---|---|---|
| NCT01569412 | Phase 1/Phase 2 (Phase 2) | Mar 1, 2012 | J. W. Goethe University |
| NCT00522457 | Phase 2 | Jan 1, 2008 | Dartmouth University, Fresenius, Neovii Biotech |
| NCT00452140 | Phase 2 | Mar 1, 2007 | Neovii Biotech, Universidad Autonoma de Barcelona |
| NCT00351858 | Phase 2 | Jul 1, 2006 | Neovii Biotech |
Organizations
Research & Development (5)
| Organization | Org type | Trials | As lead sponsor | Phases | Earliest year |
|---|---|---|---|---|---|
| Neovii Biotech | For profit | 3 | 3 | 1 | 2006 |
| Dartmouth University | Academic/Hospital | 1 | 0 | 1 | 2008 |
| Fresenius | For profit | 1 | 0 | 1 | 2008 |
| J. W. Goethe University | Academic/Hospital | 1 | 1 | 1 | 2012 |
| Universidad Autonoma de Barcelona | Academic/Hospital | 1 | 0 | 1 | 2007 |