Advanced Solid Tumor Clinical Trial
Official title:
A Phase I Dose-Escalation First-In-Human Trial to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of the Oral MEK Inhibitor MSC2015103B Administered With Two Different Treatment Schedules in Subjects With Advanced Solid Tumors
The main purpose of this study is to test the experimental drug, MSC2015103B at different
dose levels and on different treatment schedules, to see whether it is safe and can be
tolerated when given to subjects once a day one day per week over a 21-day period or once a
day three times per week over a 21-day period. The investigators would also like to find out
how MSC2015103B is broken down by the body.
Additional purposes of the trial are to assess side effects of MSC2015103B and to find out
whether MSC2015103B has anti-cancer effects. In addition, the investigators would like to
explore pharmacokinetics.
n/a
Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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