Study of Vinorelbine Liposomes Injection for Advanced Solid Tumors, Non-Hodgkin's Lymphoma or Hodgkin's Disease

The objectives of this study are:

- To assess the safety and tolerability of treatment with VLI.

- To determine the maximum tolerated dose (MTD) of VLI.

- To characterize the pharmacokinetic (PK) profile of VLI.

- To explore preliminary tumor response of VLI.

Inclusion Criteria:

1. Histologically confirmed solid tumor refractory to standard therapy or for which no
standard therapy is known to exist, or relapsed and/or refractory non-Hodgkin's
lymphoma or Hodgkin's disease

2. Adequate hematologic, hepatic and renal functions as defined by laboratory tests.

3. At least 18 years of age.

4. Have a life expectancy of at least 12 weeks.

5. Patients must give written informed consent.

6. ECOG or Zubrod performance status of 0, 1, or 2.

Exclusion Criteria:

1. Primary tumors of central nervous system (CNS). Symptomatic brain metastases (unless
patient is stable without requirement of steroids and/or antiseizure medications for
at least 3 months) or leptomeningeal tumor involvement.

2. Prior chemotherapy or radiotherapy within 4 weeks prior to study entry (6 weeks for
nitrosoureas and mitomycin C).

3. Planned concurrent systemic therapy and/or radiotherapy drug study treatment.

4. Use of investigational drugs, biologics or devices within 28 days prior to study
treatment or planned use during the course of the study.

5. Active infection or any serious underlying medical condition, which would impair the
ability of the patient to receive protocol treatment.

6. Prophylactic hematologic growth factors administered less than or equal to 2 weeks
prior to start of therapy with VLI (excluding darbepoetin alfa, epoetin alfa).

7. Female patients who are pregnant or lactating.

8. Dementia or significantly altered mental status that would prohibit the understanding
and giving of informed consent.