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

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.
AuthorsR V Smalley, D Goldstein, D Bulkowski, C Hannon, D Buchler, C Knudsen, R L Tuttle
JournalInvestigational new drugs (Invest New Drugs) Vol. 10 Issue 2 Pg. 107-12 (Jul 1992) ISSN: 0167-6997 [Print] United States
PMID1500264 (Publication Type: Clinical Trial, Journal Article)
Chemical References
  • Antigens, Tumor-Associated, Carbohydrate
  • Antineoplastic Agents
  • Chrysenes
  • Propylene Glycols
  • crisnatol
Topics
  • Aged
  • Aged, 80 and over
  • Antigens, Tumor-Associated, Carbohydrate (drug effects)
  • Antineoplastic Agents (therapeutic use)
  • Carcinoma (drug therapy, immunology)
  • Chrysenes (therapeutic use)
  • Drug Administration Schedule
  • Drug Evaluation
  • Female
  • Humans
  • Middle Aged
  • Ovarian Neoplasms (drug therapy, immunology)
  • Propylene Glycols (therapeutic use)
  • Treatment Outcome

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