Rovelizumab
| Monoclonal antibody | |
|---|---|
| Type | Whole antibody |
| Source | Humanized (from mouse) |
| Target | CD11, CD18[1] |
| Clinical data | |
| Trade names | LeukArrest |
| ATC code |
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| Identifiers | |
| CAS Number | |
| ChemSpider |
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Rovelizumab, also known as LeukArrest and Hu23F2G, is a humanized monoclonal antibody which was an experimental immunosuppressive drug. Rovelizumab was developed by Icos to treat patients suffering from haemorrhagic shock.[2] The drug is a monoclonal antibody that suppresses white blood cells which become overly active during shock.[3][4] During testing the number of patients given the drug was low because rovelizumab had to be delivered within four hours of the injury and consent was required.[4] Often the patient was unconscious and relatives had to be reached to give consent.[4] In June 1998, Icos and many medical centers asked the United States Food and Drug Administration (FDA) to waive consent requirements in situations where the patient was at high risk of dying and relatives could not be reached.[4] While some medical ethicists opposed waiving consent, the FDA approved the proposal in August 1998 for five medical centers.[5][6] Development of rovelizumab was halted in April 2000 when interim data from phase III clinical trials did not meet Icos's goals.[7] The company's goals for rovelizumab included reducing the chance of multiple organ failure and reducing the death-rate from shock at 28 days.[2] Rovelizumab was also being tested for treating heart attack, multiple sclerosis, and stroke, and was being explored as a treatment for cerebral vasospasm, head trauma, kidney transplantation, and restenosis.[1]
Multiple companies have tried to develop anti-CD18 drugs, but none of them have been successful.[8] Among them are Genentech's erlizumab, and two drugs developed by Protein Design Labs and Centocor.[8] Although trials in humans have not gone well, the research of anti-CD18 drugs in animals has been encouraging.[8] It is thought that the experimental medicines are affecting the lymphocyte adhesion pathway in humans in unintended ways.[8]
References
- ^ a b Jones R (April 2000). "Rovelizumab (ICOS Corp)". IDrugs. 3 (4): 442–6. PMID 16100700.
- ^ a b Reed, Kristin (June 15, 1999). "Icos Shares Skid After Drug Fails Test in Treating Shock". The Seattle Times. p. C7. Retrieved January 10, 2009.
{{cite news}}: Unknown parameter|name-list-format=ignored (|name-list-style=suggested) (help) - ^ Ervin, Keith (June 21, 1998). "Deep Pockets + Intense Research + Total Control = The Formula—Bothell Biotech Icos Keeps The Pipeline Full Of Promise". The Seattle Times. p. F1. Retrieved January 10, 2009.
{{cite news}}: Unknown parameter|name-list-format=ignored (|name-list-style=suggested) (help) - ^ a b c d Gorlick, Arthur (August 29, 1997). "New 'Trauma Drug' is Saving Lives; Hope Comes For Severely Injured Patients". The Seattle Post-Intelligencer. p. C1.
{{cite news}}: Unknown parameter|name-list-format=ignored (|name-list-style=suggested) (help) - ^ Lerner, Maura (June 23, 1998). "HCMC Seeks Feedback On Plans To Test Trauma Drug; Doctors Hope to Test a Medicine That Could Save Lives of Patients Who Are Unable to Speak For Themselves". Star Tribune. p. 1A.
{{cite news}}: Unknown parameter|name-list-format=ignored (|name-list-style=suggested) (help) - ^ "Community consultation and public disclosure information for waiver of Informed Consent" (PDF). Food and Drug Administration. August 27, 1998. Retrieved January 12, 2009.
- ^ "Icos Halts Stroke-Drug Study After Late Results Disappoint". The Seattle Times. April 21, 2000. p. C6. Retrieved January 10, 2009.
- ^ a b c d Dove A (August 2000). "CD18 trials disappoint again". Nature Biotechnology. 18 (8): 817–8. doi:10.1038/78412. PMID 10932141.