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



Status:Recruiting
Healthy:No
Age Range:18 - Any
Updated:2/14/2019
Start Date:September 27, 2018
End Date:September 2020
Contact:Vanda Pharmaceuticals
Email:clinicaltrials@vandapharma.com
Phone:202-734-3400

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


Inclusion 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

Exclusion Criteria:

- Allogenic 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
We found this trial at
5
sites
Seattle, Washington 98104
Phone: 202-734-3400
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Fairway, Kansas 66205
Phone: 202-734-3400
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Hackensack, New Jersey 07601
Phone: 202-734-3400
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Lafayette, Indiana 47905
Phone: 202-734-3400
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Washington, District of Columbia 20007
Phone: 202-734-3400
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Washington,
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