A Study to Investigate the Bioequivalence of Two Different Forms of Entrectinib (Forms A and C) Under Fasted Conditions in Healthy Subjects

Inclusion Criteria:

- Healthy in the opinion of the investigator. Healthy is defined by the absence of
evidence of any active disease or clinically significant medical condition based on a
detailed medical history and examination

- Negative test results for Hepatitis B, Hepatitis C, and Human Immunodeficiency Virus
(HIV)

- Females must not be pregnant or breastfeeding, and females of childbearing potential
will agree to use highly-effective contraception. Females of childbearing potential
must also agree to refrain from donating eggs during the treatment period and for 6
weeks after the final dose of study drug

- Males must agree to use contraception and to refrain from sperm donation from check-in
(Day -1 of Period 1) to 90 days after the final dose of study drug

Exclusion Criteria:

- History of gastrointestinal surgery or other gastrointestinal disorder that might
affect absorption of medicines from the gastrointestinal tract

- Presence of a clinically significant disease, illness, medical condition or disorder,
or any other medical history determined by the investigator to be clinically
significant and relevant. Ongoing chronic disorders which are not considered
clinically significant are permissible providing they are stable

- Clinically significant change in health status, as judged by the investigator, or any
major illness within the 4 weeks before screening, or clinically significant acute
infection or febrile illness within the 14 days before screening

- Participation in any other clinical study involving an investigational medicinal
product (IMP) or device within 30 days or 5 half-lives (if known), whichever is
longer, before screening