Inclusion Criteria:

- Patient ages more than 18 years old

- Patient should voluntarily sign a written informed consent before study entry

- Patient historically or cytologically confirmed diagnosis of advanced solid tumor and
patient with measurable disease or evaluable disease by RECIST criteria

- Progressive disease with development of new lesions or an increase in preexisting
lesions or standard therapy in order to provide clinical benefit does not exist or is
no longer effective

- Previous anti-cancer therapies must be completed before 21days of first study dose
and Patient must have recovered from any previous therapy

- Patient has an Eastern Cooperative Oncology Group (ECOG) Performance Status 0-1

- Patient has a life expectancy of at least 3 months

- Baseline studies for determining eligibility must be completed within 14 days of
first study dose and patient has a adequate organ function including the following:

- Hb ≥ 10g/dl

- ANC ≥ 1.5 X 109/L

- Platelet count ≥ 100 X 109/L

- Serum total bilirubin ≤ 1.5 mg/dL

- Serum AST and ALT ≤ 2.5 X UNL

- Serum ALP ≤ 2.5ⅹUNL

- Serum creatinine ≤ 1.5 X UNL

Exclusion Criteria:

- Patient has had a major surgery except tumor ablation within 2 weeks before screening
visit

- Patient has a brain metastasis with neurologic symptom

- Patient has a sensory neuropathy or motor neuropathy ≥ grade 2 by NCI-CTCAE

- Patient has any serious concurrent disease such as:

Any medical or psychiatric condition that, in the opinion of the investigator, would
prohibit the understanding and giving of informed consent Severe cardiovascular disease
(e.g. ischemic heart disease requiring medication or myocardial infraction within the past
six months, grade 3-4 congestive heart failure defined by the New York Heart Association
criteria) Active un controlled infection.

- Patient has hypersensitivity to the Investigational product or their excipients

- Patient has participated in any other clinical trial within 4 weeks before screening
visit

- Woman is pregnant or breast feeding

- Subjects who are of childbearing potential who do not use a medically acceptable
method of birth control or do not agree to continue use of this method throughout the
trial (screening, treatment period, and 3 weeks from the last done). A negative
pregnancy test (urine or serum) should be documented within 14 days prior to
initiation of trial medication for women of childbearing potential who have not been
amenorrheic for at least 12 months prior to registration into the trial or surgically
sterile (bilateral tubal ligation, bilateral oophorectomy or hysterectomy). Medically
acceptable methods include:

- Barrier method with spermicide

- Intrauterine device

- Complete abstinence, etc.

- Patient who has a history of resistance, intolerance, or no response to Docetaxel
therapy