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Continuation Protocol for ZEN003694 in Patients Experiencing Clinical Benefit While Enrolled in a ZEN003694 Protocol

Trial Status: Enrolling by Invitation

Continuation Protocol for ZEN003694 in Patients Experiencing Clinical Benefit While Enrolled in a ZEN003694 Protocol

Inclusion Criteria

  • Protocol-defined completion in a parent ZEN003694 trial
  • Patient has clinical benefit as determined by the investigator at the time of entry to the continuation protocol
  • ECOG performance status of 0 or 1
  • Acceptable ZEN003694 tolerability, in the judgment of the investigator
  • Initiation of dosing in this continuation trial to occur within two weeks (14 days) of completing dosing in the parent trial, unless more time is approved by the sponsor in writing

Exclusion Criteria

  • Concurrent participation in another clinical investigational treatment trial
  • Require addition of or change to a new concomitant therapy to adequately treat the malignancy under study
  • Discontinued ZEN003694 or withdrew consent to participate in original Zenith Epigenetics-sponsored ZEN003694 study
  • Any other reason that in the opinion of the Investigator would prevent the patient from completing participation or following the study schedule

California

San Francisco
UCSF Medical Center-Mount Zion
Status: ACTIVE
Contact: Helen Diller Family Comprehensive Cancer Center
Phone: 877-827-3222

Oregon

Portland
OHSU Knight Cancer Institute
Status: CLOSED_TO_ACCRUAL

This is an open label, non-randomized, single-arm continuation protocol study using ZEN003694. Patients who have completed participation in their original ("parent") ZEN003694 protocol and have clinical benefit as determined by the investigator may continue to receive treatment with ZEN003694 in the continuation protocol. The patient must have been enrolled in a Zenith Epigenetics sponsored ZEN003694 therapeutic study to be eligible for participation in this continuation protocol.

Trial Phase Phase I/II

Trial Type Treatment

Lead Organization
Zenith Epigenetics

  • Primary ID ZEN003694-500
  • Secondary IDs NCI-2019-07571
  • Clinicaltrials.gov ID NCT04145375