Tefibazumab: Difference between revisions
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Updating {{drugbox}} (changes to verified fields - added verified revid - updated 'UNII_Ref', 'ChEMBL_Ref', 'ChEBI_Ref', 'StdInChI_Ref', 'StdInChIKey_Ref') per Chem/Drugbox validation (report [[Wikipedia talk:WikiProject_Pharmacol... |
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<!-- Monoclonal antibody data --> |
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| type = mab |
| type = mab |
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| mab_type = mab |
| mab_type = mab |
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| source = zu/o |
| source = zu/o |
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| target = [[Clumping factor A]] |
| target = [[Clumping factor A]] |
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| CAS_number = 521079-87-8 |
| CAS_number = 521079-87-8 |
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| UNII_Ref = {{fdacite|changed|FDA}} |
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| UNII = SBO7Q9G95R |
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| molecular_weight = 147.590 [[kDa]] |
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'''Tefibazumab''' ( |
'''Tefibazumab''' (named '''Aurexis''' but not approved) is a [[humanized monoclonal antibody]] for the treatment of severe infections with ''[[Staphylococcus aureus]]''. Possible indications include the treatment of ''S. aureus'' in a phase 2a patients with [[cystic fibrosis]]<ref>{{ClinicalTrialsGov|NCT00198289|Aurexis in Cystic Fibrosis Subjects Chronically Colonized With Staphylococcus Aureus in Their Lungs}}</ref> and of [[methicillin-resistant Staphylococcus aureus|methicillin-resistant ''S. aureus'']].<ref>{{cite journal | vauthors = Pan A, Lorenzotti S, Zoncada A | title = Registered and investigational drugs for the treatment of methicillin-resistant Staphylococcus aureus infection | journal = Recent Patents on Anti-Infective Drug Discovery | volume = 3 | issue = 1 | pages = 10–33 | date = January 2008 | pmid = 18221183 | doi = 10.2174/157489108783413173 }}</ref> |
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It was developed by Inhibitex.<ref name="pmid17078388">{{cite journal | |
It was developed by Inhibitex.<ref name="pmid17078388">{{cite journal | vauthors = John JF | title = Drug evaluation: tefibazumab--a monoclonal antibody against staphylococcal infection | journal = Current Opinion in Molecular Therapeutics | volume = 8 | issue = 5 | pages = 455–60 | date = October 2006 | pmid = 17078388 }}</ref> |
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==See also== |
== See also == |
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* [[MSCRAMM]] (microbial surface components recognizing adhesive matrix molecules) |
* [[MSCRAMM]] (microbial surface components recognizing adhesive matrix molecules) |
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==References== |
== References == |
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{{reflist}} |
{{reflist}} |
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[[Category:Monoclonal antibodies]] |
[[Category:Monoclonal antibodies]] |
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[[Category:Experimental monoclonal antibodies]] |
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{{antiinfective-drug-stub}} |
{{antiinfective-drug-stub}} |
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{{monoclonal-antibody-stub}} |
{{monoclonal-antibody-stub}} |
Latest revision as of 20:57, 1 December 2023
Monoclonal antibody | |
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Type | Whole antibody |
Source | Humanized (from mouse) |
Target | Clumping factor A |
Clinical data | |
Trade names | Aurexis |
ATC code |
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Identifiers | |
CAS Number | |
ChemSpider |
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UNII | |
KEGG | |
Chemical and physical data | |
Formula | C6548H10122N1730O2034S44 |
Molar mass | 147035.72 g·mol−1 |
(what is this?) (verify) |
Tefibazumab (named Aurexis but not approved) is a humanized monoclonal antibody for the treatment of severe infections with Staphylococcus aureus. Possible indications include the treatment of S. aureus in a phase 2a patients with cystic fibrosis[1] and of methicillin-resistant S. aureus.[2]
It was developed by Inhibitex.[3]
See also
[edit]- MSCRAMM (microbial surface components recognizing adhesive matrix molecules)
References
[edit]- ^ Clinical trial number NCT00198289 for "Aurexis in Cystic Fibrosis Subjects Chronically Colonized With Staphylococcus Aureus in Their Lungs" at ClinicalTrials.gov
- ^ Pan A, Lorenzotti S, Zoncada A (January 2008). "Registered and investigational drugs for the treatment of methicillin-resistant Staphylococcus aureus infection". Recent Patents on Anti-Infective Drug Discovery. 3 (1): 10–33. doi:10.2174/157489108783413173. PMID 18221183.
- ^ John JF (October 2006). "Drug evaluation: tefibazumab--a monoclonal antibody against staphylococcal infection". Current Opinion in Molecular Therapeutics. 8 (5): 455–60. PMID 17078388.