Solid Tumors Clinical Trial
Official title:
A Phase 1 Study of S-3304 in Patients With Solid Tumors
| Verified date | April 2018 |
| Source | Shionogi Inc. |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
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
| Status | Completed |
| Enrollment | 32 |
| Est. completion date | March 12, 2003 |
| Est. primary completion date | February 13, 2003 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years to 85 Years |
| Eligibility |
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 |
| Country | Name | City | State |
|---|---|---|---|
| United States | Roswell Park Cancer Center | Buffalo | New York |
| United States | Cleveland Clinic Foundation | Cleveland | Ohio |
| United States | University of Colorado Hospital | Denver | Colorado |
| United States | H. Lee Moffitt Concer Center and Research Institute | Tampa | Florida |
| Lead Sponsor | Collaborator |
|---|---|
| Shionogi |
United States,
Chiappori AA, Eckhardt SG, Bukowski R, Sullivan DM, Ikeda M, Yano Y, Yamada-Sawada T, Kambayashi Y, Tanaka K, Javle MM, Mekhail T, O'bryant CL, Creaven PJ. A phase I pharmacokinetic and pharmacodynamic study of s-3304, a novel matrix metalloproteinase inh — View Citation
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