A Study to Assess the Safety, Pharmacokinetics, and Preliminary Efficacy of ATG 016 Monotherapy in Patients With Advanced Solid Tumors

Inclusion Criteria:

1. Understand and voluntarily sign informed Consent (ICF) prior to anyassessment/procedure related to study.
2. Age ≥18 years at ICF signature.
3. Estimated life expectancy of minimum of 12 weeks.
4. Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1 at ICF signature.
5. Subjects must have at least one measurable lesion as defined by RECIST version 1.1.
6. Females of childbearing potential must agree to use effective contraception from thetime ICF signature until 180 days after the last dose. Females of childbearingpotential include those who are premenopausal and those who are 2 yearspostmenopausal. Blood pregnancy tests must be negative for female of childbearingpotential must have a negative serum pregnancy test at Screening. Inclusion Criteria Only for Phase Ib study (Dose Escalation and Expansion phase)
7. Histological or cytological confirmation of a solid tumor, and have progressed despitestandard therapy(ies), or are intolerant to standard therapy(ies), or have no standardtherapy(ies) exists. Inclusion Criteria Only for Phase II
8. Penile squamous cell carcinomas confirmed by cytology or histology cannot be excisedby radical surgery, or postoperative recurrence or metastasis which is not suitablefor platinum chemotherapy or platinum resistance or platinum failure.
9. Nasopharyngeal carcinoma

Exclusion Criteria: Subjects with any of the following conditions will not be enrolled in this study.

1. Central nervous system (CNS) metastases and involvement.
2. A history of bone marrow or organ transplantation.
3. Prior ATG-016 administration or other XPO1 inhibitor treatment.
4. Known to be allergic to the active or inactive ingredients of ATG-016 or drugs withsimilar chemical structure, or the subject is hypersensitive.
5. Prior therapy with any investigational drugs or systemic anticancer treatment (eg, aperiod of 5 'half-lives' of drugs, whichever is longer) within 28 days at the time ofICF signature.
6. Received extensive radiation within 28 days at the time of ICF signature or expect toundergo radical radiotherapy during the study period.
7. Received major surgery within 28 days at the time of ICF signature or expect toproceed a major surgical treatment during the study period.
8. Any toxicities unresolved to Grade 1 or baseline from prior anti-tumor therapy (According to NCI-CTCAE 5.0) with the exception of alopecia, within 28 days at thetime of ICF signature.
9. Any uncontrolled active infection requiring parenteral treatment of antibiotics,antivirals, or antifungals at the time of ICF signature or within one week of Cycle 1Day 1 (C1D1). Active hepatitis B virus (HBV) infection (Hepatitis B surface antigen [HBsAg] positive) or active HCV infection (HCV-RNA positive at screening).
10. A history of HIV infection and/or acquired immunodeficiency syndrome.
11. Received immunosuppressive medication within 14 days at the time of ICF signature.
12. Cardiovascular diseases of clinical significance
13. Inadequate bone marrow reserve or organ function as demonstrated by any of thefollowing laboratory values:
14. Have a history of another primary malignancy within 5 years prior to starting studytreatment, with following exceptions: malignancy tumors treated by radical therapy andhave not been recurred, such as carcinoma in situ of the cervix, basal cell carcinomaor squamous cell carcinoma of the skin, papillary thyroid carcinoma, etc.
15. Inability or unwillingness to comply with the requirement for oral drugadministration, or presence of a gastrointestinal diseases or other clinicalconditions that would compromise the absorption of study drug, eg, refractory nauseaand vomiting, inability to swallow the formulated product, or previous significantbowel resection, etc.
16. Active or a history of bleeding within 6 months.
17. Received any live attenuated vaccination within 28 days at the signature of ICF.
18. Judgment by the investigator that the subject should not participate in the study byconsideration of the complications or other conditions which might affect theiradherence to the protocol.
19. Female subjects who are pregnant or lactating.