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Trabedersen, a TGFbeta2-specific antisense oligonucleotide for the treatment of malignant gliomas and other tumors overexpressing TGFbeta2.

Abstract
Trabedersen (AP-12009), which is being developed by Antisense Pharma GmbH, is a synthetic antisense oligodeoxynucleotide designed to block the production of TGFbeta2, a secreted protein that can exert protumor effects. Trabedersen is indicated for the treatment of malignant brain tumors and other solid tumors overexpressing TGFbeta2, such as those of the skin, pancreas and colon. Preclinical studies demonstrated that trabedersen reduced the secretion of TGFbeta2 in cultured tumor cells and exhibited antitumor activity ex vivo. It was also demonstrated that chronic intracerebral or intravascular administration of trabedersen did not cause life-threatening side effects in animals. This observation was confirmed in early clinical trials in patients with advanced cancer. In a phase IIb trial, improved survival was observed in patients with brain tumors who were intratumorally administered trabedersen, compared with patients receiving standard chemotherapy. However, this observation requires validation by an ongoing large-scale, phase III, randomized, controlled trial. Meanwhile, continued research on trabedersen should help to determine the roles of TGFbeta2 in cancer and also further the development of antisense technology.
AuthorsLuc Vallières
JournalIDrugs : the investigational drugs journal (IDrugs) Vol. 12 Issue 7 Pg. 445-53 (Jul 2009) ISSN: 2040-3410 [Electronic] England
PMID19579166 (Publication Type: Journal Article)
Chemical References
  • Antineoplastic Agents
  • Oligodeoxyribonucleotides
  • Oligonucleotides, Antisense
  • Thionucleotides
  • Transforming Growth Factor beta2
  • Trabedersen
Topics
  • Animals
  • Antineoplastic Agents (administration & dosage, adverse effects, pharmacokinetics, therapeutic use)
  • Brain Neoplasms (drug therapy, metabolism, pathology)
  • Cell Line, Tumor
  • Clinical Trials as Topic
  • Drug Evaluation, Preclinical
  • Glioma (drug therapy, metabolism, pathology)
  • Humans
  • Neoplasms (drug therapy, metabolism, pathology)
  • Oligodeoxyribonucleotides (administration & dosage, adverse effects, pharmacokinetics, therapeutic use)
  • Oligonucleotides, Antisense (administration & dosage, adverse effects, pharmacokinetics, therapeutic use)
  • Thionucleotides (administration & dosage, adverse effects, pharmacokinetics, therapeutic use)
  • Transforming Growth Factor beta2 (antagonists & inhibitors)

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