Lymphoma Clinical Trial
Official title:
A Phase I, Open-label, Dose Escalation Study to Assess the Safety, Tolerability & Pharmacokinetics of AZD4877 Administered Once Weekly in Adult Patients With Recurrent or Refractory AML, PH Negative ALL, NHL or MN
The primary purpose of this study is to find out what the maximum tolerated dose is for an experimental drug called AZD4877 based on the side effects experienced by patients that receive AZD4877 on a weekly basis in these diseases.
| Status | Terminated |
| Enrollment | 75 |
| Est. completion date | August 2007 |
| Est. primary completion date | |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - Patients with AML, a certain type of ALL, NHL and MM - certain types of cancer of the lymph nodes - certain types of leukemias (blood cancers) - disease has or will fail with other treatments - relatively good overall health other than your cancer Exclusion Criteria: - poor bone marrow function (not producing enough blood cells) - serious heart conditions - poor liver or kidney function |
Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| Canada | Research Site | Toronto | Ontario |
| United States | Research site | Buffalo | New York |
| United States | Research Site | New York | New York |
| Lead Sponsor | Collaborator |
|---|---|
| AstraZeneca |
United States, Canada,
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