The primary objective of this study is to evaluate the effectiveness of zanzalintinib + MK-3475A and zanzalintinib alone compared with placebo.
Key Inclusion Criteria:
Key Exclusion Criteria:
NOTE: Other protocol defined Inclusion/Exclusion criteria may apply.
druginfo@exelixis.com
This is a partially blinded trial: the arm of zanzalintinib + MK-3475A is an open-label arm; the arms of zanzalintinib monotherapy and placebo are blinded.
Participants will receive zanzalintinib in combination with MK-3475A (pembrolizumab + berahyaluronidase alfa) for up to 2 years.
Participants will receive zanzalintinib for up to 2 years.
Participants will receive placebo to match zanzalintinib for up to 2 years.
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