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Basiliximab

Pharmaceutical drug


Pharmaceutical drug

FieldValue
Verifiedfieldschanged
verifiedrevid459525440
typemab
mab_typemab
sourcexi/o
targetCD25
tradenameSimulect
Drugs.com
MedlinePlusa612013
licence_EUyes
DailyMedIDBasiliximab
pregnancy_AUD
routes_of_administrationIntravenous
classImmunosuppressants
ATC_prefixL04
ATC_suffixAC02
legal_AU
legal_BR
legal_CA
legal_DE
legal_NZ
legal_UK
legal_USRx-only
legal_US_comment
legal_EURx-only
legal_EU_comment
legal_UN
legal_statusRx-only
elimination_half-life7.2 days
CAS_number_Ref
CAS_number179045-86-4
DrugBank_Ref
DrugBankDB00074
ChemSpiderID_Ref
ChemSpiderIDnone
UNII_Ref
UNII9927MT646M
KEGGD03058
ChEMBL_Ref
ChEMBL1201439
C6378H=9844N=1698O=1997S=48

| Drugs.com =

| elimination_half-life = 7.2 days

Basiliximab, sold under the brand name Simulect, is a monoclonal antibody used to prevent rejection in kidney transplants. It is a chimeric mouse-human monoclonal antibody to the α chain (CD25) of the IL-2 receptor of T cells. It is used in combination with other medicines used to prevent organ rejection.

The most common side effects (seen in more than 20% of patients) include constipation, urinary tract infections (infection of the structures that carry urine), pain, nausea (feeling sick), peripheral oedema (swelling), hypertension (high blood pressure), anemia (low red blood cell counts), headache, hyperkalaemia (high blood potassium levels), hypercholesterolaemia (high blood cholesterol levels), surgical wound complication, weight increase, increased serum creatinine (a marker of kidney problems), hypophosphataemia (low blood phosphate levels), diarrhea and upper respiratory tract infection (colds).

Basiliximab was approved for medical use in the United States and in the European Union in 1998.

Medical uses

Basiliximab is indicated for the prophylaxis of acute organ rejection in de-novo allogeneic renal transplantation. It is to be used concomitantly with ciclosporin for microemulsion- and corticosteroid-based immunosuppression, in people with panel reactive antibodies less than 80%, or in a triple maintenance immunosuppressive regimen containing ciclosporin for microemulsion, corticosteroids and either azathioprine or mycophenolate mofetil.

Basiliximab is an immunosuppressant agent used to prevent immediate transplant rejection in people who are receiving kidney transplants, in combination with other agents. It has been reported that some cases of lichen planus have been successfully treated with basiliximab as an alternative therapy to cyclosporin. No short-term side effects have been reported.

Mechanism of action

Basiliximab competes with IL-2 to bind to the alpha chain subunit of the IL2 receptor on the surface of the activated T lymphocytes and thus prevents the receptor from signaling. This prevents T cells from replicating and also from activating B cells, which are responsible for the production of antibodies, which would bind to the transplanted organ and stimulate an immune response against the transplant.

Chemistry

It is a chimeric CD25 monoclonal antibody of the IgG1 isotype.

History

It is a Novartis product and was approved by the Food and Drug Administration (FDA) in 1998.

References

References

  1. (6 October 2022). "Simulect- basiliximab injection, powder, for solution".
  2. (31 October 2009). "Simulect EPAR".
  3. (20 February 2009). "Basiliximab Product Approval Information - Licensing Action". U.S. [[Food and Drug Administration]] (FDA).
  4. MedlinePlus. Last Revised - 15 June 2012 [https://www.medlineplus.gov/druginfo/meds/a612013.html Basiliximab Injection]
  5. (2003). "European handbook of dermatological treatments". Springer.
  6. (July 2013). "Selection of induction therapy in kidney transplantation". Transplant International.
  7. "Basiliximab label".
  8. (March 2003). "Immunotherapy: past, present and future". Nature Medicine.
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