This study is not accepting new patients

Expanded Access Program for SNDX-5613

a study on Leukemia

Summary

Location
at San Francisco, California and other locations
Dates
study started

Description

Summary

This expanded access program will provide an investigational treatment option in a controlled clinical setting for patients who are not otherwise eligible to participate in a clinical study and have no approved treatment options.

Official Title

Expanded Access Program for SNDX-5613 in Patients With Relapsed/Refractory Acute Leukemias With Genetic Alterations Associated With HOXA Overexpression

Keywords

Relapsed/Refractory Acute Leukemia, SNDX-5613, Acute Leukemia, Refractory leukemia, Relapsed leukemia, KMT2A, NPM1, UBTF tandem duplication, Leukemia

Eligibility

You can join if…

  • Male or female participant aged ≥30 days.
  • Not eligible for participation in an ongoing clinical study.
  • Participant or participant's health care proxy is able and willing to provide written informed consent and able to follow study instructions.
  • Diagnosed with relapsed/refractory acute leukemia harboring a mixed lineage leukemia rearrangement, nucleoporin 98 rearrangement, nucleophosmin 1 mutation (or mutated) mutation or any other genetic alteration with overexpression of HOXA genes predicted to potentially respond to menin inhibitors.
  • Adequate liver, renal, and cardiac function

  • Adequate methods of contraception are required during childbearing age from the time of enrollment through 120 days following the last study drug dose. Barrier contraception in males and double barrier in females or other highly effective method of contraception.

    For participants currently being treated with SNDX-5613 in a Syndax-sponsored clinical study the following criteria must be met:

  • In the opinion of the Investigator, participant demonstrated acceptable benefit from and tolerability of the study drug
  • Participant is considered to be compliant with study drug and procedures
  • Participant does not meet any criteria for study drug discontinuation
  • Investigator and participant agree to continue study drug treatment

You CAN'T join if...

  • Evidence of uncontrolled infection
  • Pregnant or nursing women.
  • Cardiac or gastrointestinal disease.
  • Graft-Versus-Host Disease (GVHD): Signs or symptoms of acute or chronic GVHD >Grade 1 within 4 weeks of enrollment. All transplant patients must have been off all systemic immunosuppressive therapy for at least 1 week prior to enrollment and calcineurin inhibitors for at least 1 week, with the exception of steroids.
  • History of or any concurrent condition, therapy, laboratory abnormality, or allergy to excipients that, in the Investigator's opinion, either may interfere with the participant's participation or results in the conclusion that it is not in the best interest of the participant to participate.

Locations

  • UCSF not accepting new patients
    San Francisco California 94158 United States
  • Lucile Packard Children's Hospital-Stanford not accepting new patients
    Palo Alto California 94304 United States

Details

Status
not accepting new patients
Start Date
Sponsor
Syndax Pharmaceuticals
ID
NCT05918913
Study Type
Expanded Access
Last Updated
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