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TP-10 (AVANT Immunotherapeutics).

P Rioux1

  • 1PMB 214, Lexington, MA 02421-7934, USA. prioux@ieee.org

Current Opinion in Investigational Drugs (London, England : 2000)
|September 29, 2001
PubMed
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See all related articles

TP-10, a soluble complement receptor type 1 (sCR1), is being developed to treat reperfusion injury and organ rejection. Clinical trials in adults and infants undergoing cardiac surgery are evaluating its safety and efficacy in mitigating organ damage.

Area of Science:

  • Immunology
  • Pharmacology

Background:

  • Recombinant soluble complement receptor type 1 (sCR1), known as TP-10, is under development by AVANT Immunotherapeutics.
  • TP-10 targets complement-mediated conditions, including reperfusion injury, organ rejection, and autoimmune diseases.

Purpose of the Study:

  • To evaluate the safety and efficacy of TP-10 in preventing and reducing organ injury.
  • To assess TP-10's potential in mitigating damage during cardiopulmonary bypass in cardiac surgery patients.
  • To explore TP-10's utility in treating conditions like adult respiratory distress syndrome (ARDS) and in organ transplantation.

Main Methods:

  • Phase II placebo-controlled trials involving adult and infant patients undergoing cardiac surgery with cardiopulmonary bypass.
  • Phase I/II trials in infants undergoing cardiac surgery for congenital heart defects.

Related Experiment Videos

  • Phase I safety trials in adult patients at risk for ARDS and myocardial infarction, and in pediatric cardiac surgery patients.
  • Main Results:

    • TP-10 demonstrated favorable results in animal models of reperfusion injury and xenograft rejection.
    • Phase I trials indicated that TP-10 is well tolerated in adult and pediatric patient populations.
    • Development for ARDS was ceased following a Phase IIa trial, but TP-10 was licensed for transplantation.

    Conclusions:

    • TP-10 shows potential for treating a range of complement-mediated conditions.
    • Ongoing clinical trials aim to establish TP-10's efficacy in cardiac surgery patients.
    • Further development is planned, including pivotal Phase III trials, based on trial outcomes.