Inclusion Criteria:

          1. Patients with histologically confirmed intrahepatic, perihilar or extra-hepatic CCA.

          2. Patients with no more than 2 prior treatments with systemic anti-neoplastic therapy
             for CCA.

          3. The tumor is unresectable and not amenable to curative therapy.

          4. One or more tumors measurable on CT scan per RECIST 1.1.

          5. Eastern Cooperative Oncology Group (ECOG) performance status 0- 1.

          6. Life expectancy of at least 3 months.

          7. Age ≥18 years.

          8. Signed, written IRB-approved informed consent.

          9. A negative pregnancy test (if female).

         10. Acceptable liver and renal function:

               -  Bilirubin ≤ 1.5 times upper limit of normal (CTCAE Grade 2 baseline)

               -  AST (SGOT), ALT (SGPT) ≤ 2.5 x upper limit of normal (ULN),

               -  Serum creatinine ≤ 1.5 X ULN (CTCAE Grade 1 baseline)

               -  Albumin > 3.0 g/dL

         11. Acceptable hematologic status:

               -  Absolute neutrophil count ≥1000 cells/mm3

               -  Platelet count ≥75,000 (plt/mm3) (CTCAE Grade 1 baseline)

               -  Hemoglobin ≥ 9 g/dL

         12. Acceptable blood sugar control:

             - Fasting glucose value ≤ 160 mg/dL (CTCAE Grade 1 baseline)

         13. Urinalysis: No clinically significant abnormalities.

         14. Prothrombin time (PT) and partial thromboplastin time (PTT) ≤ 1.5 X ULN after
             correction of nutritional deficiencies that may have contributed to prolonged PT/PTT.

         15. For men and women of child-producing potential, willingness to use effective
             contraceptive methods during the study. If female (or female partner of male patient),
             was either not of childbearing potential (defined as postmenopausal for ≥ 1 year or
             surgically sterile [bilateral tubal ligation, bilateral oophorectomy or hysterectomy])
             or practicing one of the following medically acceptable methods of birth control and
             agreed to continue with the regimen throughout the duration of the study:

               -  Oral, implantable or injectable contraceptives for 3 consecutive months before
                  the baseline/randomization visit.

               -  Total abstinence from sexual intercourse (≥ 1 complete menstrual cycle before the
                  baseline/randomization visit).

               -  Intrauterine device.

               -  Double barrier method (condoms, sponge, diaphragm or vaginal ring with
                  spermicidal jellies or cream

        Exclusion Criteria:

          1. >2 previous systemic anti-neoplastic regimens for CCA.

          2. Previously having received ABC294640 or HCQ (or chloroquine) for the treatment of a
             malignancy.

          3. New York Heart Association Class III or IV, cardiac disease, myocardial infarction
             within the past 6 months, unstable arrhythmia, or evidence of ischemia on ECG.

          4. Active, uncontrolled bacterial, viral, or fungal infections, requiring systemic
             therapy.

          5. Pregnant or nursing women. NOTE: If a woman became pregnant or suspects she is
             pregnant while participating in this study, she must inform her treating physician
             immediately.

          6. Treatment with radiation therapy, surgery, chemotherapy, or investigational therapy
             within 28 days prior to study entry.

             Patients who had received any antineoplastic therapy > 28 days prior to starting
             treatment with ABC294640 and HCQ must have recovered from the reversible effects of
             prior antineoplastic therapy (with the exception of alopecia and Grade 1 neuropathy).

          7. Unwillingness or inability to comply with procedures required in this protocol.

          8. Known infection with human immunodeficiency virus.

          9. Serious nonmalignant disease (e.g., hydronephrosis, liver failure, or other
             conditions) that could compromise protocol objectives in the opinion of the
             investigator and/or the sponsor.

         10. Patients who were currently receiving any other investigational agent.

         11. Patients who were receiving drugs that were sensitive substrates of CYP450 1A2, 3A4,
             2C9, 2C19 or 2D6, or strong inhibitors or inducers of all major CYP450 isozymes that
             could not have been stopped at least 7 days or 5 half-lives (whichever was longer)
             before starting treatment with ABC294640, could not have been replaced with another
             appropriate medication or not given for the duration of the clinical study must be
             discussed with the Medical Monitor in order to determine eligibility for the study.

         12. Patients who are taking warfarin, apixaban, argatroban or rivaroxaban.

         13. If the patient is to receive HCQ, pre-existing retinopathy.

         14. Known history of G-6-PD Deficiency, porphyria or psoriasis.

         15. History of macular degeneration, visual field changes, retinal disease, or cataracts
             that would interfere with funduscopic eye examinations.

         16. History of allergic reactions attributed to compounds of similar chemical or biologic
             composition to HCQ.