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Clinical Trial Summary

This is a non-blinded, multi-center, open-label, phase 2 study to evaluate the activity, safety, and tolerability of Oraxol in subjects with cutaneous angiosarcoma.


Clinical Trial Description

Oraxol will be administered once daily for 3 consecutive days every week during the Treatment Period from Weeks 1 through 25. Subjects who do not have documented disease progression by the end of the Treatment Period will be eligible to receive therapy in the Treatment Extension Period; Oraxol may be administered from Week 26 onwards. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03544567
Study type Interventional
Source Athenex, Inc.
Contact
Status Completed
Phase Phase 2
Start date December 21, 2018
Completion date May 12, 2023

See also
  Status Clinical Trial Phase
Terminated NCT03921073 - Study of T-VEC in Locally Advanced Cutaneous Angiosarcoma Phase 2