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Clinical Trial Summary

The purpose of this program is to provide participants an early access to erdafitinib prior to market authorization (that is, Food and Drug Administration [FDA] approval in the United States). The program is limited to participants with advanced cancers and fibroblast growth factor receptor (FGFR) genetic alterations who have exhausted at least 2 lines of standard of care therapy and who are not eligible for an erdafitinib clinical trial.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Advanced Cancers and FGFR Genetic Alterations
  • Neoplasms

NCT number NCT03825484
Study type Expanded Access
Source Janssen Scientific Affairs, LLC
Contact
Status Approved for marketing
Phase