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A Phase 1 Study of S-3304 in Patients with Solid Tumors



A Phase 1 Study of S-3304 in Patients with Solid Tumors

For Condition: Solid Tumors
Status: No longer recruiting
Sponsor(s): Shionogi ,
Synopsis: To determine the maximum tolerated dose and safety profile of S-3304 in patients with biopsy accessible cancer who have failed previous therapy or to whom no standard therapies are available. To determine the pharmacokinetic profile of S-3304 in this patient population
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety Study
Minimum Age/Maximum Age: 18 Years/85 Years
Genders: Both
Protocol Entry Criteria: Inclusion criteria: -Biopsy proven diagnosis of solid tumor(s) with biopsy accessible lesion(s) -Must be able to tolerate oral medication Exclusion criteria -Patients with other serious illnesses -Patients who are receiving treatments
Total Enrollment: 28

Location and Contact Information:

Rush-Presbyterian-St. Lukes Medical Center
Chicago,  Illinois,  60612
United States
 

Cleveland Clinic Foundation
Cleveland,  Ohio,  44195
United States
 

University of Colorado Hospital
Denver,  Colorado,  80262
United States
 

Roswell Park Cancer Center
Buffalo,  New York,  14263
United States
 


Additional Information:
Study ID Numbers:
  0110P1416; 
Study Start Date: November 2001
Record last reviewed: November 2003
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00033215

Other Solid Tumors Studies:
1. Colony-Stimulating Factors in Treating Children With Recurrent or Refractory Solid Tumors

2. A Phase 1 Study of S-3304 in Patients with Solid Tumors

3. Phase I study of PN401, fluorouracil, leucovorin and CPT-11 in patients with solid tumors

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