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Pharmatech 516-001

Trial Overview

Official Title

A Phase I/Ib Study of MGCD516 in Patients With Advanced Solid Tumor Malignancies

Study Purpose

To identify how much MGCD516 can safely be administered, how much study drug is absorbed after taking MFCD516 capsules orally and how quickly the study drug is cleared from the blood stream.

Diagnosis

Metastatic or unresectable solid tumor malignancy

Eligibility

Metastatic or unresectable solid tumor malignancy; Standard treatment is not available; Adequate bone marrow and organ function.

Patients must sign an approved informed consent and authorization permitting release of personal health information.

Intervention

  • MGCD516, study agent (oral medication) taken daily
  • You may remain on this study for as long as your disease doesn’t get worse such that the study doctor feels you should stop study treatment, and as long as you tolerate the study drug (MGCD516).
  • At the end of the study you will be contacted every 2 months by study staff

For more information, visit the U.S. National Library of Medicine clinical trial database.

Key Participation Requirements
Trial Location(s)
Methodist Estabrook Cancer Center
Gender
Male or Female
Age
19 years and older
Enrollment Status
Available
Phase
Phase IB
Methodist Health System Trial Code
Pharmatech 516-001
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