atacicept
Atacicept is a recombinant fusion protein designed to inhibit B cells, thereby suppressing autoimmune disease. The designer protein combines the binding site for two cytokines that regulate maturation, function, and survival of B cells – B-lymphocyte stimulator (BLyS) and A proliferation-inducing ligand (APRIL), with the constant region of immunoglobin. Atacicept blocks activation of B cells by the tumor necrosis factor receptor superfamily member 13B, a transmembrane receptor protein found predominantly on the surface of B cells. Like the monoclonal antibody belimumab, atacicept blocks the binding of BLyS, but it also blocks APRIL. Binding of these TACI ligands induces proliferation, activation, and longevity of B cells and thus their production of autoantibodies. Atacicept is thought to selectively impair mature B cells and plasma cells with less impact on progenitor cells and memory B cells. — Wikipedia
Clinical trial activity
18 trials · 4 clinical orgs · 0 marketing orgs
Earliest trial started Dec 1, 2006 (NCT00430495)
Timeline
Indications
Studied for
- Arthritis, Rheumatoid · Phase 2
- Diabetic Nephropathies · Phase 2
- Glomerulonephritis, IGA · Phase 2
- Glomerulosclerosis, Focal Segmental · Phase 2
- Kidney Diseases · Phase 2
- Lupus Erythematosus, Systemic · Phase 2/Phase 3
- Lupus Nephritis · Phase 3
- Lymphoma, Large B-Cell, Diffuse · Phase 2
- Nephrotic Syndrome · Phase 2
- Optic Neuritis · Phase 2
- Urologic Diseases · Phase 2
Mechanism of action
TNFSF13 inhibitor
Soluble receptor. Acts as a decoy receptor for TNFSF13 (APRIL) and TNFSF13B (BAFF).
TNFSF13B inhibitor
Soluble receptor. Acts as a decoy receptor for TNFSF13 (APRIL) and TNFSF13B (BAFF).
Chemistry & pharmacology
- Chirality
- Single Stereoisomer
- Inorganic
- No
- Polymer
- No
- Multi-specific
- No
Oral
No
Parenteral
No
Topical
No
Sources
- WikipediaAtacicept ↗
- ChEMBLCHEMBL1742986 ↗
Also known as
- atacicept
- atacicept
- atacicept
- taci-fc5
- taci-ig
- taci-ig
- taci receptor-igg fc fragment fusion protein
Clinical trials
| NCT ID | Phase | Start date | Sponsor(s) |
|---|---|---|---|
| NCT06983028 | Phase 2 | Jul 7, 2025 | Vera Therapeutics, Inc. |
| NCT07020923 | Phase 2 | May 29, 2025 | Vera Therapeutics, Inc. |
| NCT06674577 | Phase 2 | Dec 1, 2024 | Vera Therapeutics, Inc. |
| NCT05609812 | Phase 3 | Nov 2, 2022 | Vera Therapeutics, Inc. |
| NCT04716231 | Phase 2 | May 18, 2021 | Vera Therapeutics, Inc. |
| NCT02808429 | Phase 2 | Jan 31, 2017 | Merck KGaA, Merck Serono |
| NCT02070978 | Phase 2 | Jul 29, 2014 | Merck Serono |
| NCT01972568 | Phase 2 | Dec 1, 2013 | Merck Serono |
| NCT01440231 | Phase 2 | Feb 1, 2012 | Merck KGaA, Merck Serono |
| NCT01369628 | Phase 1 | Jun 1, 2011 | Merck Serono |
| NCT00853762 | Phase 2 | Mar 1, 2009 | Merck KGaA, Merck Serono |
| NCT00624468 | Phase 2 | Jun 1, 2008 | Merck KGaA, Merck Serono |
| NCT00642902 | Phase 2 | Apr 1, 2008 | Merck KGaA, Merck Serono |
| NCT00664521 | Phase 2 | Mar 1, 2008 | Merck KGaA |
| NCT00624338 | Phase 2/Phase 3 (Phase 3) | Jan 1, 2008 | Merck KGaA, Merck Serono |
| NCT00573157 | Phase 2/Phase 3 (Phase 3) | Dec 1, 2007 | Merck Serono, ZymoGenetics |
| NCT00595413 | Phase 2 | Sep 1, 2007 | Merck KGaA, Merck Serono |
| NCT00430495 | Phase 2 | Dec 1, 2006 | Merck KGaA, Merck Serono |
Organizations
Research & Development (4)
| Organization | Org type | Trials | As lead sponsor | Phases | Earliest year |
|---|---|---|---|---|---|
| Merck Serono | For profit | 12 | 12 | 3 | 2006 |
| Merck KGaA | For profit | 9 | 1 | 2 | 2006 |
| Vera Therapeutics, Inc. | For profit | 5 | 5 | 2 | 2021 |
| ZymoGenetics | For profit | 1 | 0 | 1 | 2007 |