A Clinical Trial of Oral Suberoylanilide Hydroxamic Acid (SAHA) in Patients With Relapsed or Refractory Breast, Colorectal and Non-Small Cell Lung Cancer (0683-011)(TERMINATED)
Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Merck Sharp & Dohme LLC
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Patient must be 18 years or older with confirmed diagnosis of breast adenocarcinoma, colorectal carcinoma or non-small cell lung cancer
Patients must have relapsed or refractory disease following at least one chemotherapeutic treatment regimen.
Has a measurable, positron emission tomography (PET) assessable lesion
Adequate blood, liver, bone marrow and kidney functions
Has not received any chemotherapy for at least 4 weeks prior to entry in this study
Agrees to take adequate measures to prevent pregnancy.
You may not be if
Patient has had prior treatment with histone deacetylase (HDAC) inhibitor.
Patient has had treatment with investigational agents within the last 30 days.
Patient has active infection or had intravenous (IV) antibiotic, antiviral, or antifungal medications within 2 weeks of the start of study drugs.
Patient has HIV, hepatitis B or hepatitis C infection.
Patient is pregnant or lactating.
Patient has allergy to any component of the study drug.
Clareo Health | A Clinical Trial of Oral Suberoylanilide Hydroxamic Acid (SAHA) in Patients With Relapsed or Refractory Breast, Colorectal and Non-Small Cell Lung Cancer (0683-011)(TERMINATED)
