Suberoylanilide Hydroxamic Acid in Advanced Solid Tumors

• Status: Completed
• Trial end date: 2007-12-01
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this investigational study is to determine the safety and tolerability of oral suberoylanilide hydroxamic acid when administered in combination with standard doses of pemetrexed and cisplatin for the treatment of advanced solid tumors.

• Phase: Phase 1
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Merck Sharp & Dohme Corp.
• Treatments: Cisplatin; Pemetrexed; Vorinostat

Criteria

Inclusion Criteria:

• Patient must be 18 years or older with confirmed diagnosis of a solid tumor for which pemetrexed and cisplatin is acceptable treatment and have received no more than 2 prior systemic therapies

• Has at least 1 measurable lesion

• Has adequate blood, liver, 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 as outlined in the protocol

Exclusion Criteria:

• Patient has been treated with other investigational agents with a similar anti-tumor mechanism

• Patient from Cohorts A and B has received pemetrexed or cisplatin within the past 6 months and from Cohorts C and D have received pemetrexed within the past 6 months

• Patient from Cohorts A and B has preexisting Grade 2 or higher neuropathy and from Cohorts C and D have Grade 3 or higher neuropathy

• Patient has active infection or had received IV (intravenous) 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 breast feeding

• Patient has allergy to any component of the study drugs

• Patient has history of GI (gastrointestinal) surgery or conditions