drugset / Trial / NCT00002136

A Phase I Trial of Tecogalan Sodium (DS-4152) Administered as an Infusion Every 21 Days

NCT00002136 ↗

Phase 1 Completed Daiichi Pharmaceuticals
Treatment

Summary

To evaluate the safety of different doses and dosing regimens of tecogalan sodium (DS-4152) and to establish the MTD at each of the different dosing schedules.

Timeline

Start
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Primary completion
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Completion
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Publications

  • Background Eckhardt SG, et al. Results of a phase I trial of the novel angiogenesis inhibitor, tecogalan sodium (meeting abstract). Proc Annu Meet Am Assoc Cancer Res. 1995; 36:A628

Drugs

EvaluationDrugModalityDoseRoute
Subject Tecogalan Unknown — Intravenous