UCN-01 Kyowa Hakko Kogyo Co

Curr Opin Investig Drugs. 2001 Feb;2(2):287-97.

Abstract

Kyowa Hakko Kogyo is developing UCN-01, a selective but non-specific inhibitor of kinases with good activity against protein kinase C (PKC) and the cyclin-dependent kinases (CDKs). This hydroxylated derivative of staurosporine has potential for the treatmentfor cancer [154087], [311028], and may be useful in the treatment of chronic lymphocytic leukemia [312089]. It is in phase I clinical trials [321641], [326004], [326256]. At the 11th NCI-EORTC-AACR Symposium (Amsterdam, November 2000), a presentation was made on UCN-01. In the initial clinical trial, in which UCN-01 was administered by continuous infusion for 72 h, a prolonged half-life of 600 h was observed. The MTD was 42.5 mg/m2/day x 3. One patient with refractory melanoma achieved a partial response, another patient with refractory anaplastic large cell lymphoma had no evaluable diseasefor more than three years [391376].

Publication types

  • Review

MeSH terms

  • Alkaloids / adverse effects
  • Alkaloids / metabolism
  • Alkaloids / pharmacology*
  • Alkaloids / toxicity
  • Animals
  • Antineoplastic Agents / adverse effects
  • Antineoplastic Agents / metabolism
  • Antineoplastic Agents / pharmacology*
  • Antineoplastic Agents / toxicity
  • Apoptosis / drug effects
  • Clinical Trials, Phase I as Topic
  • Clinical Trials, Phase II as Topic
  • Clinical Trials, Phase III as Topic
  • Contraindications
  • Enzyme Inhibitors / pharmacology*
  • Humans
  • Protein Kinase C / antagonists & inhibitors*
  • Staurosporine / analogs & derivatives
  • Structure-Activity Relationship

Substances

  • Alkaloids
  • Antineoplastic Agents
  • Enzyme Inhibitors
  • 7-hydroxystaurosporine
  • Protein Kinase C
  • Staurosporine