alemtuzumab (Campath-1H, Lemtrada)

From Aaushi
Jump to navigation Jump to search

Indications

* on list of drugs to avoid for treatment of muliple sclerosis[6]

  • disproportionate adverse effects cited

Contraindications

Dosage

  • 12 mg IV daily for 5 days at baseline, then daily for 3 days at 12 months

Monitor

Adverse effects

* compared with 66% for IFN-beta-1a (infections)

Mechanism of action

Notes

Manufacturer: Berlex

More general terms

Additional terms

References

  1. Prescriber's Letter 9(2):S1 2002
  2. Jump up to: 2.0 2.1 Cohen JA et al. Alemtuzumab versus interferon beta 1a as first-line treatment for patients with relapsing-remitting multiple sclerosis: A randomised controlled phase 3 trial. Lancet 2012 Nov 24; 380:1819. PMID: https://www.ncbi.nlm.nih.gov/pubmed/23122652
    Coles AJ et al. Alemtuzumab for patients with relapsing multiple sclerosis after disease-modifying therapy: A randomised controlled phase 3 trial. Lancet 2012 Nov 24; 380:1829. PMID: https://www.ncbi.nlm.nih.gov/pubmed/23122650
  3. Jump up to: 3.0 3.1 3.2 3.3 3.4 Medical Knowledge Self Assessment Program (MKSAP) 16, 17, 18. American College of Physicians, Philadelphia 2012, 2015, 2018.
  4. Jump up to: 4.0 4.1 Galper SL, Smith BD, Wilson LD. Diagnosis and management of mycosis fungoides. Oncology (Williston Park). 2010 May;24(6):491-501. PMID: https://www.ncbi.nlm.nih.gov/pubmed/20568590
  5. Jump up to: 5.0 5.1 Genzyme's Lemtrada Approved by the FDA Manufacturer's Press Release. November 14, 2014 http://news.genzyme.com/press-release/genzymes-lemtrada-approved-fda
  6. Jump up to: 6.0 6.1 6.2 Therapeutics Letter #108. Therapeutics Initiative Drugs to Avoid. http://www.ti.ubc.ca/2018/01/04/108-drugs-avoid/
  7. Jump up to: 7.0 7.1 FDA Safety Announcement. Nov 29, 2018 FDA warns about rare but serious risks of stroke and blood vessel wall tears with multiple sclerosis drug Lemtrada (alemtuzumab). https://www.fda.gov/Drugs/DrugSafety/ucm624247.htm