A First-in-human Study of IBI354 in Subjects with Locally Advanced Unresectable or Metastatic Solid Tumors

Inclusion Criteria:

1. Male or female subjects, ≥ 18 years

2. Phase 1a : Has a pathologically documented advanced/unresectable or metastatic solidtumor with HER2 alterations (IHC 1+, IHC 2+, IHC 3+ and/or ISH+ and/or NGS confirmedmutant or amplification). Phase 1b/2: Selected solid tumors enrolled Subjects with advanced GC/BC/BTC/CRC/Gynwith her2 expression (IHC 1+, IHC 2+, IHC 3+ and/or ISH+).

3. Adequate bone marrow and organ function

4. Subjects, both male and female, who are either not of childbearing potential or whoagree to use at least one highly effective method of contraception during the study (begin from screening or within 2 weeks prior to the first dose, whichever comesfirst, and continue until 6 months after the last dose of study drug); Subjects,both male and female, who are either not of childbearing potential or who agree touse a highly effective method of contraception during the study beginning within 2weeks prior to the first dose and continuing until 6 months after the last dose ofstudy drug

5. Subjects with the ability to understand and give written informed consent forparticipation in this trial, including all evaluations and procedures as specifiedby this protocol;

6. Have LVEF ≥ 50% by echocardiography (ECHO) within 28 days before study drugadministration.

Exclusion Criteria:

1. Received previous anti-tumor therapy within 4 weeks or 5 half-lives of theanti-tumor regimens before the first administration of study drug, whichever isshorter;

2. Plan to receive other antitumor therapy during the study excluding palliativeradiotherapy for the purpose of symptom (like pain) relief that must also do nothave impact on tumor assessment throughout the study;

3. Potent cytochrome P450 3A4 (CYP3A4) inhibitors within 2 weeks or 5 half-lives (whichever is longer) before first administration of the study drug.

4. Has adverse reactions resulting from previous antitumor therapies, which have notresolved to Grade 0 or 1 toxicity according to NCI-CTCAE v5.0 (except for alopecia,fatigue, pigmentation and other conditions with no safety risk according toinvestigators' opinion) or baseline prior to first administration of the study drug;

5. Known symptomatic central nervous system (CNS) metastases.

6. History of pneumonia requiring corticosteroids therapy, or history of clinicallysignificant lung diseases or who are suspected to have these diseases by imaging atscreening period;

7. Uncontrolled diseases including:

• Uncontrolled infection requiring systematic antibiotics, antivirals orantifungals within 2 weeks prior to first administration of the study drug;

• Known human immunodeficiency virus (HIV) infection, or HIV positive (HIV 1/2 Abpositive);

• HBsAg positive and/or HBcAb positive with HBV DNA titer ≥ 104 copies/mL or ≥ 2000 IU/mL or higher than lower limit of detection or HCV Ab positive with HCVRNA>103 copies/mL;

• Active infection with COVID-19;

• Active tuberculosis infection, or still on anti-tuberculosis therapy orreceived anti-tuberculosis therapy within 1 year prior to first administrationof the study drug;

• Active syphilis infection or latent syphilis requiring treatment;

• Symptomatic congestive heart failure Grade II-IV, symptomatic or uncontrolledarrhythmias, QTc interval > 480 ms or personal or family history of congenitallong/short QT syndrome;

• SBP ≥ 160mmHg or DBP ≥ 100mmHg;

8. History of any arterial thromboembolic event within 6 months prior to the firstadministration of study drug, including myocardial infarction, unstable anginapectoris, cerebrovascular stroke or transient ischemic attack, etc.;

9. Risk of intestinal obstruction or perforation (including but not limited to: acutediverticulitis, abdominal abscess, etc.) or a history of inflammatory bowel disease,Crohn's disease, ulcerative colitis, or chronic diarrhea;

10. Do not have adequate treatment washout period before study drug administration,defined as:

• Major surgery; ≥ 4 weeks.

• Radiation therapy；≥ 4 weeks (if palliative stereotactic radiation therapy, ≥ 2weeks).

• Autologous transplantation；≥ 3 months.

• Hormonal therapy；≥ 2 weeks.

• Chemotherapy (including antibody drug therapy or other antitumor therapy)； ≥ 3weeks.

• Immunotherapy； ≥ 4 weeks.

• Cytochrome P450 (CYP) 3A4 strong inhibitor；≥ 3 elimination half-lives of theinhibitor.