OncoMatch

OncoMatch/Clinical Trials/NCT03838926

Tolerability Study of Trichostatin A In Subjects With Relapsed or Refractory Hematologic Malignancies

Is NCT03838926 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1 trial studies Trichostatin A for relapsed or refractory hematologic malignancies.

Phase 1RecruitingVanda PharmaceuticalsNCT03838926Data as of Jun 2026Location: United States · Poland

Treatment: Trichostatin AThe aim of this study is to investigate the safety and tolerability of trichostatin A in individuals with relapsed or refractory hematologic malignancies.

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Extracted eligibility criteria

Treatments studied

Other

Trichostatin A

Cancer type

Acute Myeloid Leukemia

Acute Lymphoblastic Leukemia

Non-Hodgkin Lymphoma

Multiple Myeloma

Myelodysplastic Syndrome

Chronic Lymphocytic Leukemia

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Lab requirements

Cardiac function

Impaired cardiac function or conduction defect [excluded]

Impaired cardiac function or conduction defect

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Vanda Investigational Site · Washington D.C., District of Columbia
  • Vanda Investigational Site · Lafayette, Indiana
  • Vanda Investigational Site · Hackensack, New Jersey
  • Vanda Investigational Site · Seattle, Washington

Showing up to 5 US sites.

See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT03838926 currently recruiting?

Yes, this trial is currently recruiting patients.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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