A Phase I Study of MK8669 in Patients With Metastatic or Locally Advanced Solid Tumors
Interventional
Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Any clinical or laboratory adverse experience.
Duration of Treatment
Yes
Medical Monitor
Study Director
Merck
Japan: Pharmaceuticals and Medical Devices Agency
2008_011
NCT00694083
June 2008
September 2009
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