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RECRUITING Phase 1

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

NCT03838926 · View on ClinicalTrials.gov ↗

Study Summary

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

Interventions

  • DRUG Trichostatin A

Study Locations (11)

Other

  • Vanda Investigational Site — Biała Podlaska
  • Vanda Investigational Site — Katowice
  • Vanda Investigational Site — Krakow
  • Vanda Investigational Site — Opole
  • Vanda Investigational Site — Skorzewo
  • Vanda Investigational Site — Warsaw
  • Vanda Investigational Site — Wroclaw

District of Columbia

  • Vanda Investigational Site — Washington D.C.

Indiana

  • Vanda Investigational Site — Lafayette

New Jersey

  • Vanda Investigational Site — Hackensack

Washington

  • Vanda Investigational Site — Seattle

Trial Details

FieldValue
Enrollment Target 42 participants
Start Date 2018-09-27
Est. Completion 2027-12
Phase Phase 1

Sponsor

Vanda Pharmaceuticals

34 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03838926

The ClinicalTrials.gov registry entry for NCT03838926 describes a study currently listed as recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 42 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Vanda Pharmaceuticals, which has 34 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Relapsed or Refractory Hematologic Malignancies appearing as the primary indexed condition, and to 1 intervention — of which Trichostatin A is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03838926 reports 11 study locations spanning 5 distinct geographic areas — top geographies include Other, District of Columbia, Indiana. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT03838926 about?

NCT03838926 is a clinical study titled "Tolerability Study of Trichostatin A In Subjects With Relapsed or Refractory Hematologic Malignancies". The aim of this study is to investigate the safety and tolerability of trichostatin A in individuals with relapsed or refractory hematologic malignancies.

What is the current status of trial NCT03838926?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 42 participants. The study started on 2018-09-27. Estimated completion is 2027-12.

What conditions does trial NCT03838926 study?

This clinical trial studies the following conditions: Relapsed or Refractory Hematologic Malignancies. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03838926?

The interventions under investigation include: Trichostatin A (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03838926?

This trial is sponsored by Vanda Pharmaceuticals, which has 34 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03838926 being conducted?

This trial has 11 study locations across District of Columbia, Indiana, New Jersey, Washington. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial