Inclusion Criteria:

          -  Signed, written Institutional Review Board (IRB)-approved Informed Consent Form (ICF).

          -  Histologically confirmed locally advanced unresectable (Stage III) or Stage IV PDAC.

          -  Measurable or evaluable disease on computed tomography (CT) or magnetic resonance
             imaging (MRI) scan per RECIST v1.1.

          -  For patients with locally advanced disease, no previous radiotherapy, surgery,
             chemotherapy, or investigational therapy for the treatment of PDAC is permitted. For
             patients with metastatic disease, prior treatment for non-metastatic disease with 5-FU
             or gemictabine administered as radiation sensitizer, or as a cytotoxic therapy, in the
             adjuvant setting is allowed, provided at least 6 months have elapsed since completion
             of the last dose and no ≥ Grade 2 treatment-related toxicities are present.

          -  Karnofsky Performance Status ≥70%.

          -  Life expectancy ≥3 months.

          -  Age ≥18 years.

          -  A negative serum pregnancy test, if female of reproductive potential.

          -  Screening clinical laboratory values as follows, performed within 14 days prior to day
             1:

               -  Total bilirubin ≤1.5 times upper limit of normal (ULN).

               -  Aspartate aminotransferase ([AST]; serum glutamic oxaloacetic transaminase
                  [SGOT]) and alanine aminotransferase ([ALT]; serum glutamic pyruvate transaminase
                  [SGPT]) ≤2.5 times ULN, (if liver metastases are present, then ≤5 times ULN is
                  allowed).

               -  Serum creatinine ≤2.0 mg/dL or calculated creatinine clearance ≥60 mL/min.

               -  Serum albumin ≥3.0 g/dL.

               -  Absolute neutrophil count (ANC) ≥1,500 cells/mm3.

               -  Platelet count ≥100,000 plt/mm3.

               -  Hemoglobin ≥9 g/dL

               -  Prothrombin time (PT)/international normalized ratio (INR) within normal limits
                  (±15%) or within therapeutic range if on warfarin.

               -  Partial thromboplastin time (PTT) within normal limits (±15%).

          -  For men and women of reproductive potential, agreement to use an effective
             contraceptive method from the time of screening and throughout their time on study.
             Effective contraceptive methods consist of prior sterilization, intra-uterine device,
             oral or injectable contraceptives, and/or barrier methods. Abstinence alone is not
             considered an adequate contraceptive measure for the purposes of this study.

        Exclusion Criteria:

          -  Known central nervous system involvement or brain metastases.

          -  New York Heart Association Class III or IV cardiac disease or myocardial infarction
             within the past 12 months.

          -  Known, clinically significant carotid artery disease.

          -  Known, increased risk of bleeding.

          -  Patients with TE event occurring > 6months prior to enrollment and receiving active
             anticoagulation.

          -  Patients with any prior history of arterial thrombosis or symptomatic pulmonary
             embolism.

          -  Patients with current use of megestrol acetate (use with 10 days of Day 1) will be
             excluded.

          -  Active, uncontrolled bacterial, viral, or fungal infection requiring systemic therapy.

          -  Known active infection with human immunodeficiency virus, hepatitis B, or hepatitis C.

          -  Known allergy to hyaluronidase.

          -  Patients with prosthetic heart valves

          -  Women currently pregnant or breastfeeding.

          -  Intolerance of dexamethasone.

          -  History of another primary cancer within the last 3 years with the exception of
             non-melanoma skin cancer or curatively-treated cervical carcinoma in-situ.

          -  History of transient ischemic attack (TIA) or cerebrovascular accident (CVA).

          -  Any other disease, metabolic dysfunction, physical examination finding or clinical
             laboratory finding that leads to reasonable suspicion of a disease or condition that
             contraindicates the use of an investigational drug, that may affect the interpretation
             of the results, or that may render the subject at high risk for treatment
             complications.

          -  Other unspecified reasons that, in the opinion of the Investigator, make the subject
             unsuitable for the study.

          -  Inability to comply with study and follow-up procedures as judged by the Investigator.