Inclusion Criteria:
- ECOG performance status 0 or 1
- Estimated life expectancy of at least 3 months
- Patients who have progressed on or after all available standard therapies or for whom standard treatment is inappropriate
- Mandatory provision of archived or fresh tumor tissue in quantity sufficient to allow for retrospective confirmation of HER2 or EGFR mutation
- A patient with a history of brain metastases must have had all lesions treated
- Adequate organ function defined as all of the following:
- Adequate bone marrow function (within 1 week prior to first administration): Neutrophils≥1.5 x10\*9 cells/L (Criteria must be met without the use of Granulocyte-Colony Stimulating Factor (G-CSF) within last week prior to testing.); platelet count≥75 x10\*9 cells/L; Hb ≥9g/dL (Criteria must be met without packed red blood cell (pRBC) transfusion within last week prior to testing.)
- Adequate hepatic function: Serum bilirubin≤1.5 x upper limit of normal (ULN), and serum transaminase (either aspartate transaminase (AST) or alanine transaminase (ALT)) ≤ 3 x ULN if no demonstrable liver metastases, or otherwise ≤ 5 x ULN if transaminase elevation is attributable to liver metastases (within 1 week prior to first administration)
- Adequate renal function: Serum creatinine ≤ 1.5 x ULN or Estimated glomerular filtration rate (eGFR) > 60 mL/min per 1.73 m\*2 according to the site's calculation method.
\[Dose Escalation part only\]
- Histologically or cytologically confirmed diagnosis of advanced, and/or metastatic non-hematologic malignancy
- Documented HER2 or EGFR mutation (HER2 mutation or EGFR exon 20 insertion, HER2 amplification or overexpression)
\[Dose Expansion part only\]
- Patients with histologically or cytologically confirmed locally advanced or metastatic NSCLC HER2 exon 20 insertion (Cohort 1)
Exclusion Criteria:
- Patient with symptomatic or progressive brain metastases
- Known or suspected leptomeningeal disease (LMD)
- Uncontrolled spinal cord compression
- History of acute coronary syndromes, including myocardial infarction, coronary artery bypass graft, unstable angina, coronary angioplasty or stenting within past 24 weeks
- History of or current Class II, III or IV heart failure as defined by the New York Heart Association (NYHA) functional classification system
- Medical, psychiatric, cognitive or other conditions that compromise the patients ability to understand the patient information, to give informed consent, to comply with the study protocol or to complete the study
- Any severe concurrent disease or condition (includes active infections, cardiac arrhythmia) that in the judgment of the Investigator would make study participation inappropriate for the patient
- History of (non-infectious) interstitial lung disease (ILD) or pneumonitis that required steroids, or any evidence of current ILD or pneumonitis
- History of a second primary cancer with the exception of
1. curatively treated non-melanomatous skin cancer,
2. curatively treated cervical or breast carcinoma in situ, or
3. other malignancy with no known active disease present and no treatment administered during the last 2 years
- Infection with human immunodeficiency virus (HIV) or prior hepatitis B or active chronic hepatitis B or active hepatitis C
- Major surgery within 4 weeks prior to the first dose of study treatment