18
Participants
Start Date
October 17, 2019
Primary Completion Date
December 16, 2019
Study Completion Date
December 16, 2019
Tepotinib 100 mg
Participants received a single oral dose of test treatment of tepotinib TF3 (5 \* 100 mg) in either treatment period 1 or 2.
Tepotinib 250 mg
Participants received a single oral dose of reference treatment of tepotinib TF3 (2 \* 250 mg) in either treatment period 1 or 2.
Nuvisan GmbH, Neu-Ulm
Merck Healthcare KGaA, Darmstadt, Germany, an affiliate of Merck KGaA, Darmstadt, Germany
INDUSTRY