A phase II study of crisnatol mesylate in patients with ovarian carcinoma

Invest New Drugs. 1992 Jul;10(2):107-12. doi: 10.1007/BF00873127.

Abstract

Fourteen patients with advanced ovarian cancer received a 72 hour infusion of a new DNA intercalator, crisnatol mesylate, administered intravenously. There was no evidence of antitumor efficacy. A syndrome of nausea and vomiting associated with vertigo, dizziness and ataxia was observed in nearly all patients. Two of the patients developed severe CNS toxicity manifested in one by a grand-mal seizure and in the other by peripheral neuropathy. Further explorations into the potential efficacy of crisnatol mesylate administered intraperitoneally are underway.

Publication types

  • Clinical Trial

MeSH terms

  • Aged
  • Aged, 80 and over
  • Antigens, Tumor-Associated, Carbohydrate / drug effects
  • Antineoplastic Agents / therapeutic use*
  • Carcinoma / drug therapy*
  • Carcinoma / immunology
  • Chrysenes / therapeutic use*
  • Drug Administration Schedule
  • Drug Evaluation
  • Female
  • Humans
  • Middle Aged
  • Ovarian Neoplasms / drug therapy*
  • Ovarian Neoplasms / immunology
  • Propylene Glycols / therapeutic use*
  • Treatment Outcome

Substances

  • Antigens, Tumor-Associated, Carbohydrate
  • Antineoplastic Agents
  • Chrysenes
  • Propylene Glycols
  • crisnatol