Belatacept

(Nulojix®)

Belatacept

Drug updated on 11/1/2024

Dosage FormInjection (intravenous; 250 mg)
Drug ClassSelective T-cell costimulation blockers
Ongoing and
Completed Studies
ClinicalTrials.gov

Indication

  • Indicated in combination with basiliximab induction, mycophenolate mofetil, and corticosteroids for prophylaxis of organ rejection in adult patients receiving a kidney transplant.

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Summary
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  • This summary is based on the review of five systematic review(s)/meta-analysis(es). [1-5]
  • In hand transplants, 65.9% of patients experienced rejection, and 13.2% experienced graft loss; in face transplants, rejection occurred in 73% of patients, with a graft loss rate of 8.9%.
  • Among hand transplant recipients, clinical CMV infection was observed in 6.6% of patients, while in face transplant recipients, the rate was 15.5%.
  • For kidney transplants, no significant differences in efficacy and safety were noted between once-daily and twice-daily tacrolimus regimens; however, regimens involving calcineurin inhibitor avoidance and early steroid withdrawal were associated with increased rejection rates.
  • In hand and face transplants, nephrotoxicity required modifications to standard triple maintenance therapy, with clinical CMV infection rates observed at 6.6% for hand transplants and 15.5% for face transplants.
  • For kidney transplants, tacrolimus was associated with new-onset diabetes, nephrotoxicity, and electrolyte imbalances; belatacept showed a lower incidence of new-onset diabetes but carried a higher risk of infection, including EBV-related lymphoproliferative disorders, and had a reduced vaccine response.
  • There is no population types or subgroups information available in the reviewed studies.