Pantothenic Acid |
Calcium Pantothenate; Vitamin B5 |
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Clinical Trial: A Study of Oral Suberoylanilide Hydroxamic Acid (SAHA) in Patients with Malignant Lymphoma
This study is currently recruiting patients.
Verified by Merck August 2005
|
Purpose
The primary purpose of this trial is to determine the maximum tolerated dose (MTD), or the maximum acceptable dose (MAD) and evaluate the dose limiting toxicity (DLT) of oral suberoylanilide hydroxamic acid in patients with malignant lymphoma.
| Condition | Intervention | Phase |
|---|---|---|
| Malignant Lymphoma | Drug: MK0683, Suberoylanilide hydroxamic acid (SAHA) | Phase I |
MedlinePlus related topics: Lymphoma
Study Type: Interventional
Study Design: Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety Study
Eligibility
Ages Eligible for Study: 20 Years - 75 Years, Genders Eligible for Study: Both
Criteria
Inclusion Criteria:
- Patients who relapsed after complete or partial response, or ineffective in previous chemotherapy
Exclusion Criteria:
Location and Contact Information
Please refer to this study by ClinicalTrials.gov identifier NCT00127140
Call For Information +81-3-5203-8218
Japan, Chuoku
Call For Site Information, Tokyo, Chuoku, 103-8416, Japan; Recruiting
Study chairs or principal investigators
Medical Monitor, Study Director, Merck
More Information
Study ID Numbers: 2005_041
Last Updated: August 19, 2005
Record first received: August 3, 2005
ClinicalTrials.gov Identifier: NCT00127140
Health Authority: Japan: Ministry of Health, Labor and Welfare
ClinicalTrials.gov processed this record on 2005-08-23
Last Updated: August 19, 2005
Record first received: August 3, 2005
ClinicalTrials.gov Identifier: NCT00127140
Health Authority: Japan: Ministry of Health, Labor and Welfare
ClinicalTrials.gov processed this record on 2005-08-23
Resources
- Calcium Pantothenate (Drug Digest)
- Pantothenic Acid (Drug Digest)

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