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Phase I clinical trial of weekly iv 2,3-dihydro-1H-imidazo[1,2-b]pyrazole (IMPY).

Abstract
In a phase I trial, 2,3-dihydro-1H-imidazo[1,2-b]pyrazole was administered iv weekly at doses ranging from 0.1 to 3.0 g/m2/wk to patients with refractory metastatic solid tumors. Although gastrointestinal toxicity was tolerable and neither granulocyte nor platelet toxicity was seen, significant dose-limiting hemolysis was encountered at doses of 1.5 g/m2/wk. While no definite tumor regressions were seen in the 32 patients evaluable for response, two patients (squamous cell carcinoma of lung and tonsil) had clinically useful improvement.
AuthorsC L Vogel, J M Denefrio, D C Padgett, M A Silverman
JournalCancer treatment reports (Cancer Treat Rep) 1980 Oct-Nov Vol. 64 Issue 10-11 Pg. 1153-6 ISSN: 0361-5960 [Print] United States
PMID7459903 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antineoplastic Agents
  • Imidazoles
  • Pyrazoles
  • 2,3-dihydro-1H-imidazo(1,2-b)pyrazole
Topics
  • Antineoplastic Agents (adverse effects, therapeutic use)
  • Drug Evaluation
  • Female
  • Humans
  • Imidazoles (adverse effects, therapeutic use)
  • Male
  • Middle Aged
  • Neoplasms (drug therapy)
  • Pyrazoles (adverse effects, therapeutic use)

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