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Clinical Trial Summary

This rollover protocol allows continued access to seclidemstat (SP-2577) for patients who are still receiving clinical benefit on completed or closed Salarius sponsored studies.


Clinical Trial Description

The population for the rollover study should be consistent with the population defined in the parent study. The primary eligibility criteria for a patient to enter the rollover protocol is the participation and completion of a Salarius sponsored study with seclidemstat. Safety data and an evaluation of anti-tumor activity will be collected. Patients who have completed a prior study with seclidemstat and who are assessed by the Investigator to continue to benefit from ongoing treatment will be eligible. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05266196
Study type Interventional
Source Salarius Pharmaceuticals, LLC
Contact
Status Enrolling by invitation
Phase Phase 1/Phase 2
Start date January 15, 2022
Completion date December 2025

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