RECRUITING

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

Description

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

Study Overview

Study Details

Study overview

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

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

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

Condition
Relapsed or Refractory Hematologic Malignancies
Intervention / Treatment

-

Contacts and Locations

Washington

Vanda Investigational Site, Washington, District of Columbia, United States, 20007

Lafayette

Vanda Investigational Site, Lafayette, Indiana, United States, 47905

Hackensack

Vanda Investigational Site, Hackensack, New Jersey, United States, 07601

Seattle

Vanda Investigational Site, Seattle, Washington, United States, 98109

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Subject is ≥ 18 years at the time of signing informed consent;
  • * Confirmed malignant hematologic disease or lymphoid malignancy that has relapsed or is refractory to standard therapy and has exhausted all available therapies;
  • * Presence of measurable or evaluable disease;
  • * Eastern Cooperative Oncology Group (ECOG) performance status of ≤ 2;
  • * Contraceptives or other approved avoidance of pregnancy measures
  • * Allogeneic stem cell transplant recipient presenting with graft versus host disease (GVHD) either active or requiring immunosuppression;
  • * Concomitantly taking anti-cancer therapy (bisphosphonates are permitted);
  • * Undergone major surgery ≤ 2 weeks prior to starting study drug;
  • * Evidence of mucosal or internal bleeding;
  • * Impaired cardiac function or conduction defect;
  • * Concurrent severe and/or uncontrolled medical conditions

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Vanda Pharmaceuticals,

Study Record Dates

2025-12