• Men or women (as appropriate for cancer type) of age ≥18 years.

• Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2.

• Histologically or cytologically confirmed diagnosis of solid tumor as documented in medical records with the primary history comprising one of the following:

∙ SCCHN

‣ NSCLC

‣ SCLC

‣ Breast cancer

‣ Cervical cancer

‣ Endometrial cancer

‣ Ovarian cancer

‣ Urothelial cancer

‣ Sarcoma

∙ Thyroid cancer

• Presence of metastatic disease that has progressed during or following previous treatment.

• Presence of radiographically measurable disease.

• Prior receipt of commercially available therapies that are indicated for the subject's cancer and have demonstrated survival benefit for that indication.

• Availability of tumor tissue from a fresh tumor biopsy obtained by a core needle, excisional, or incisional biopsy; or punch biopsy (for cutaneous disease); or archival tumor sample from a previous biopsy.

• Availability of computed tomography (CT) or magnetic resonance imaging (MRI) of chest, abdomen, and pelvis, and/or fluorodeoxyglucose (FDG) positron emission tomography (PET)/CT (if appropriate for tumor type) (with PET from base of the skull to mid-thigh, if performed) within 35 days before study drug administration.

• Completion of all previous therapy (including surgery, radiotherapy, chemotherapy, targeted therapy, immunotherapy, or investigational therapy) for the treatment of cancer ≥1 week before the start of study drug administration.

⁃ Adequate hematological profile.

⁃ Adequate coagulation profile.

⁃ Adequate hepatic profile.

⁃ Adequate renal function.

⁃ Negative viral serology or adequate therapy for human immunodeficiency virus (HIV), hepatitis B (HBV), and hepatitis C (HCV) infection.

⁃ For female subjects of childbearing potential, a negative serum pregnancy test.

⁃ For female subjects of childbearing potential, willingness to use a protocol-recommended method of contraception from the start of the screening period until ≥6 months after the final dose of study therapy.

⁃ For male subjects who can father a child and are having intercourse with females of childbearing potential who are not using adequate contraception, willingness to use a protocol-recommended method of contraception from the start of study therapy until ≥6 months after the final dose of study therapy and to refrain from sperm donation from the start of study therapy until ≥12 months after administration of the final dose of study therapy.

⁃ Willingness and ability of the subject to comply with scheduled visits, the drug administration plan, protocol-specified laboratory tests, other study procedures (including required tumor biopsy/aspirations and/or radiographic studies), and study restrictions.

⁃ Evidence of a personally signed informed consent indicating that the subject is aware of the neoplastic nature of the disease and has been informed of the procedures to be followed, the experimental nature of the therapy, alternatives, potential risks and discomforts, potential benefits, and other pertinent aspects of study participation.