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Clinical Trial Summary

The primary purpose of this study is to evaluate the tolerability, safety and pharmacokinetic profile of ASP1948 in Japanese patients with locally advanced (unresectable) or metastatic solid tumors. This study will also evaluate the antitumor effect of ASP1948.


Clinical Trial Description

This study consists of 3 dose levels (1200 milligrams [mg], 2000 mg and 3000 mg) and enrollment of subjects into dose level 1200 mg will take place first. Dose level 2000 mg would only be opened if dose level 1200 mg is deemed tolerable. Dose level 3000 mg would only be opened if dose level 2000 mg is deemed tolerable. ;


Study Design


Related Conditions & MeSH terms

  • Locally Advanced (Unresectable) or Metastatic Solid Tumor Malignancies
  • Neoplasms

NCT number NCT04094506
Study type Interventional
Source Astellas Pharma Inc
Contact
Status Completed
Phase Phase 1
Start date October 30, 2019
Completion date February 2, 2022