Inclusion Criteria:

- Men with histologically or cytologically confirmed adenocarcinoma of the prostate

- Prior treatment with one, and only one, NHT (eg, abiraterone, apalutamide,
darolutamide, or enzalutamide) for castration-sensitive locally advanced (T3 or T4) or
mCSPC, M0 CRPC, or mCRPC

- Surgical or medical castration, with serum testosterone ≤ 50 ng/dL (≤ 1.73 nmol/L) at
screening

- Measurable (extrapelvic soft tissue) metastatic disease per Investigator assessment
defined by at least one of the following: measurable visceral disease (eg, adrenal,
kidney, liver, lung, pancreas, spleen) per RECIST 1.1; OR measurable extrapelvic
adenopathy (ie, adenopathy above the aortic bifurcation)

- Progressive disease at study entry as defined by specific criteria for prostate
specific antigen (PSA) progression OR soft tissue disease progression in the opinion
of the Investigator (Note: subjects with bone disease progression alone are not
eligible)

- Age ≥ 18 years old or meeting country definition of adult, whichever is older, on the
day of consent

- ECOG performance status of 0 or 1

- Recovery to baseline or ≤ Grade 1 per Common Terminology Criteria for Adverse Events
(CTCAE) v5 from toxicities related to any prior treatments, unless AE(s) are
clinically nonsignificant and/or stable on supportive therapy in the opinion of the
Investigator

- Adequate organ and marrow function based upon specific laboratory assessments obtained
within 21 days prior to randomization

- Understanding and ability to comply with protocol requirements

Exclusion Criteria:

- Any prior nonhormonal therapy initiated for the treatment of mCRPC

- Receipt of abiraterone within 1 week; cyproterone within 10 days; or flutamide,
nilutamide, bicalutamide, enzalutamide, or other androgen-receptor inhibitors within 2
weeks before randomization

- Radiation therapy within 4 weeks (2 weeks for bone metastases) prior to randomization
(subjects with clinically relevant ongoing complications from prior radiation therapy
are not eligible)

- Known brain metastases or cranial epidural disease unless adequately treated and
clinically stable at least 4 weeks prior to randomization

- Symptomatic or impending spinal cord compression or cauda equina syndrome

- Concomitant anticoagulation with oral anticoagulants (some specific exceptions apply)

- Administration of a live, attenuated vaccine within 30 days prior to randomization

- Systematic treatment with, or any condition requiring, either corticosteroids (>10 mg
daily prednisone equivalent) or other immunosuppressive medications within 14 days
prior to randomization

- Uncontrolled, significant intercurrent or recent illness

- Major surgery within 4 weeks prior to randomization

- Corrected QT interval calculated by the Fridericia formula (QTcF) > 480 ms per ECG
within 21 days before randomization

- Inability or unwillingness to swallow pills or receive IV administration

- Previously identified allergy or hypersensitivity to components of the study treatment
formulations or history of severe infusion-related reactions to monoclonal antibodies

- Any other active malignancy at time of randomization or diagnosis of another
malignancy within 2 years prior to randomization that requires active treatment (some
exceptions apply such as locally curable cancers that have apparently been cured).

Note: Other protocol defined Inclusion/Exclusion criteria may apply.

Eligibility last updated 10/13/22. Questions regarding updates should be directed to the study team contact.