1. Histologic confirmation of BCC by local board-certified pathologist, as described in the protocol
2. At least one lesion that is measurable by study criteria, defined as ≥ 1cm in at least one dimension, as assessed by radiology and/or digital medical photography, as described in the protocol
3. The treating physician must document that the participant is not appropriate for curative-intent surgery or curative-intent radiation
4. The treating physician must document that the participant does not wish to receive a hedgehog pathway inhibitor (HHI) or is not a candidate for an HHI
5. Eastern Cooperative Oncology Group (ECOG) performance status ≤ 1
1. Documentation of histopathologic diagnosis of basal cell carcinoma - NOT necessary
2. Submission of tumor or blood for exploratory correlative research - NOT necessary
You may not be if
1. Metastatic disease to lymph node(s) or distant site(s) (Note: involvement of lymph node due to direct invasion from overlying cutaneous BCC is still considered laBCC, and is not excluded)
2. History or current evidence of significant cardiovascular disease, as described in the protocol
3. Exposure to any prior systemic therapy (eg, HHI or an immune checkpoint inhibitor) or locally injectable agent for laBCC, as described in the protocol
4. Current participation OR past participation in another investigational trial in which an investigational intervention (eg, drug, vaccine, invasive device) was administered within 4 weeks before planned first dose of study intervention in this clinical trial.
1\. Receipt of any anti-cancer therapy (including HHIs, radiation, surgery, or other systemic therapy) for BCC, AFTER treatment on Arms A, B, or C.
