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Phase 1
18 Years
N/A
Open (Enrolling)
Both
Cancer

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Trial Information


Inclusion Criteria:



- Patients with advanced solid tumors with previous treatment or beyond standard
therapy of significant clinical benefit

- Therapy with no more than 3 prior chemotherapy regimens

- Radiotherapy to less than 25% of bone marrow volume (no pelvic radiation)

- Adequate organ function

- Recovery from the effects of prior chemotherapy and radiation therapy, with at least
a 4 week interval. All prior toxicities should have resolved to baseline prior to
entry into the study.

- Good performance status

- Anticipate life expectancy of at least 6 months

- Not pregnant or lactating.

- Sexually active men and women of childbearing age must use adequate contraception.

- Be able to give signed, written informed consent.

- No gastrointestinal condition that could affect the absorption of the drug

- No active infection requiring systemic medical therapy one week prior to chemotherapy

Type of Study:

Interventional

Study Design:

Primary Purpose: Treatment

Authority:

United States: Federal Government

Study ID:

NCRR-M01RR00096-1001

NCT ID:

NCT00006199

Start Date:

Completion Date:

Related Keywords:

  • Cancer
  • solid tumor

Name

Location

NYU Cancer InstituteNew York, New York  10016