The primary objective of this long-term extension study is to allow continued access to study treatment for eligible participants who are deriving clinical benefit in an Exelixis-sponsored study who do not have access to treatment locally.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
5,000
Administered as specified in the parent study.
Administered as specified in the parent study.
Administered as specified in the parent study.
Administered as specified in the parent study.
Administered as specified in the parent study.
Administered as specified in the parent study.
Administered as specified in the parent study.
Number of Participants With Treatment Emergent Adverse Events (TEAEs)
Time frame: Up to 4 years (until the event resolves, returns to baseline, stabilizes, a new anticancer therapy is initiated, or the participant is lost to follow-up or withdraws consent, whichever occurs first)
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