A Study of ICP-192 in Patients With FGFR2-Rearranged Unresectable or Metastatic Intrahepatic Cholangiocarcinoma

Inclusion Criteria:

1. Signed the ICF and Age ≥ 18 years old, either sex.
2. ECOG score of 0-1.
3. Life expectancy > 3 months.
4. Histopathologically or cytopathologically confirmed intrahepatic cholangiocarcinomawith unresectable, recurrent or metastatic (AJCC 2017, 8th edition, TNM stage IV)tumor that has progressed following at least one line of chemotherapy andprogression/recurrence within 6 months after neoadjuvant/adjuvant chemotherapy may beincluded.
5. FGFR2 fusion /rearrangement as confirmed by the central laboratory.
6. At least one measurable lesion at screening as target lesion per RECIST 1.1.
7. Organ functions meeting the protocol requirements.
8. Contraception according to the protocol requirements.

Exclusion Criteria:

1. Presence of other malignancies requiring medical intervention.
2. Prior treatment with selective FGFR inhibitors or FGFR antibodies.
3. Treatment with biological products, radical radiotherapy, and other investigationaldrugs within 4 weeks prior to the first dose of study drug. Chemotherapy within 3weeks prior to the first dose of study drug.
4. Known symptomatic central nervous system (CNS) metastases.
5. Patients who have not recovered from the toxicity caused by previous anti-tumortreatment and have ≥ Grade 2 adverse events (judged per CTCAE V5.0 evaluationcriterion) at the first dose of study drug.
6. Currently uncontrolled cardiovascular and cerebrovascular diseases, or a past medicalhistory.
7. Any unstable or uncontrolled systemic disease as judged by the investigator, such as:active infection requiring intravenous therapy, uncontrolled hypertension (Aftertreatment systolic blood pressure ≥ 150 mmHg and/or diastolic blood pressure ≥ 90mmHg), and diabetes mellitus (HbA1c > 8%).
8. Current active bleeding, such as deep venous thrombosis, portal hypertension signsleading to gastroesophageal venous bleeding.
9. Wound with active infection.
10. Major surgical procedures within 4 weeks prior to the first dose of the study drug orminor surgical procedures within 2 weeks prior to the first dose of the study drug.
11. Any corneal or retinal abnormalities that may result in an increased risk of oculartoxicity
12. History and/or current evidence of extensive tissue calcification, including but notlimited to calcification in soft tissues, kidney, intestine, myocardium, vasculatureand/or the lungs, with the exception of lymph node calcification, mild pulmonaryparenchymal calcification, and asymptomatic coronary artery calcification.
13. Clinically serious gastrointestinal dysfunction that may affect the intake, transportor absorption of the study drug (such as poorly controlled nausea, vomiting, diarrhea;malabsorption syndrome; intestinal obstruction and small bowel resection, etc.), orthe patient was unable to swallow the drug orally.
14. Active HBV infection, Active HCV infection, HIV infection.
15. Female subjects who are pregnant or breastfeeding, or plan to have a pregnancy within 6 months after the last dose of the study drug; or male subjects who plan to father achild during the study or within 6 months after the last dose of the study drug.
16. The last dose of strong CYP3A inhibitor or CYP3A inducer (including food, westernmedicine, traditional Chinese medicine) is less than 5 half-lives before the firstdose of study drug, or plans to take concomitant drugs or foods with strong CYP3Ainhibition or induction during the study.
17. Known allergy to any excipients of the study drug.
18. Subjects with conditions that in the investigator's opinion are not suitable forparticipating in this trial.