Clazakizumab: Difference between revisions
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{{Short description|Chemical compound}} |
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{{drugbox |
{{drugbox |
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| type = mab |
| type = mab |
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| excretion = |
| excretion = |
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| CAS_number = 1236278-28-6 |
| CAS_number = 1236278-28-6 |
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| UNII_Ref = {{fdacite|correct|FDA}} |
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| UNII = 4S38Z8RA9O |
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| ATCvet = |
| ATCvet = |
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| ATC_prefix = none |
| ATC_prefix = none |
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| ChemSpiderID = none |
| ChemSpiderID = none |
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| DrugBank = |
| DrugBank = |
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| KEGG = D10312 |
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| C=6426 | H=9972 | N=1724 | O=2032 | S=42 |
| C=6426 | H=9972 | N=1724 | O=2032 | S=42 |
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| synonyms = ALD518, BMS-945429 |
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| molecular_weight = 145.2 kg/mol |
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'''Clazakizumab''' (formerly ALD518 and BMS-945429), an [[investigational drug]], is |
'''Clazakizumab''' (formerly '''ALD518''' and '''BMS-945429'''), an [[investigational drug]], is an [[aglycosylated]], humanized rabbit [[monoclonal antibody]] against [[interleukin-6]].<ref name="Handbook">{{cite book|title=Handbook of Therapeutic Antibodies, Volume 2|date=2007|publisher=Wiley Blackwell|page=987|isbn=9783527329373|url=https://books.google.com/books?id=svHsBQAAQBAJ&q=Clazakizumab,+BMS-945429+ALD518&pg=PA987|access-date=January 23, 2017}}</ref> Clazakizumab was developed by [[Bristol Myers Squib]] and [[Alder Biopharmaceuticals]]. A preliminary randomized, double-blind, [[placebo]]-controlled, [[phase 2 clinical trial|phase 2]] dose-ranging study of clazakizumab in [[psoriatic arthritis]] patients, funded by the manufacturer, suggested that clazakizumab may be an effective treatment option for musculoskeletal aspects of [[psoriatic arthritis]]; however, the antibody lacked a [[dose-response effect]].<ref name="ArthRheum1">{{cite journal|vauthors=Mease PJ, Gottlieb AB|display-authors=etal|title=The efficacy and safety of clazakizumab, an anti-interleukin-6 monoclonal antibody, in a phase IIb study of adults with active psoriatic arthritis.|journal=Arthritis Rheumatol|date=September 2016|volume=68|issue=9|pages=2163–73|doi=10.1002/art.39700|pmid=27059799|s2cid=3644962}}</ref> |
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==See also== |
==See also== |
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{{Interleukin receptor modulators}} |
{{Interleukin receptor modulators}} |
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[[Category:Bristol |
[[Category:Drugs developed by Bristol Myers Squibb]] |
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[[Category:Antibodies]] |
[[Category:Antibodies]] |
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[[Category: |
[[Category:Experimental monoclonal antibodies]] |
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[[Category:Experimental drugs]] |
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[[Category:Experimental cancer drugs]] |
Latest revision as of 07:01, 2 December 2023
Monoclonal antibody | |
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Type | Whole antibody |
Source | Humanized |
Target | IL6 |
Clinical data | |
Other names | ALD518, BMS-945429 |
Routes of administration | infusion |
ATC code |
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Legal status | |
Legal status |
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Identifiers | |
CAS Number | |
ChemSpider |
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UNII | |
KEGG | |
Chemical and physical data | |
Formula | C6426H9972N1724O2032S42 |
Molar mass | 145239.02 g·mol−1 |
Clazakizumab (formerly ALD518 and BMS-945429), an investigational drug, is an aglycosylated, humanized rabbit monoclonal antibody against interleukin-6.[1] Clazakizumab was developed by Bristol Myers Squib and Alder Biopharmaceuticals. A preliminary randomized, double-blind, placebo-controlled, phase 2 dose-ranging study of clazakizumab in psoriatic arthritis patients, funded by the manufacturer, suggested that clazakizumab may be an effective treatment option for musculoskeletal aspects of psoriatic arthritis; however, the antibody lacked a dose-response effect.[2]
See also
[edit]- Tocilizumab (Actemra) an anti-IL-6 receptor mAb
- Anti-IL-6, other anti-interleukin-6 agents
References
[edit]- ^ Handbook of Therapeutic Antibodies, Volume 2. Wiley Blackwell. 2007. p. 987. ISBN 9783527329373. Retrieved January 23, 2017.
- ^ Mease PJ, Gottlieb AB, et al. (September 2016). "The efficacy and safety of clazakizumab, an anti-interleukin-6 monoclonal antibody, in a phase IIb study of adults with active psoriatic arthritis". Arthritis Rheumatol. 68 (9): 2163–73. doi:10.1002/art.39700. PMID 27059799. S2CID 3644962.