A Phase 1 interventional study of ARRY-382, cFMS inhibitor; oral in Metastatic Cancer, sponsored by Array Biopharma, now a wholly owned subsidiary of Pfizer. Completed at 2 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2020-09-21.
Sponsored by Array Biopharma, now a wholly owned subsidiary of Pfizer · Phase 1, Interventional, and Treatment
This is a Phase 1 study during which patients with advanced cancer will receive investigational study drug ARRY-382. Patients will receive increasing doses of study drug in order to achieve the highest dose of the study drug possible that will not cause unacceptable side effects. Patients will be followed to see what side effects and effectiveness the study drug has, if any, in treating the cancer. Approximately 50 patients from the US will be enrolled in this study.
3,517 studies on the registry are indexed under Neoplasm Metastasis; 885 are open to participants now.
This study's enrollment of 26 is below the median of 54 across 2,767 interventional studies indexed under Neoplasm Metastasis.
Browse Neoplasm Metastasis studies →Array Biopharma, now a wholly owned subsidiary of Pfizer is the lead sponsor of 25 studies on the registry; none are open to participants now.
Counted across the registry records on this site, refreshed daily.
Key Inclusion Criteria:
Key Exclusion Criteria:
Drug: ARRY-382, cFMS inhibitor; oral
multiple dose, escalating
Characterize the safety profile of the study drug as determined by adverse events, clinical laboratory tests and electrocardiograms.
Time frame: Safety will be characterized for the duration of time that each patient stays on study; estimated one year.
Establish the maximum tolerated dose (MTD) of study drug.
Time frame: The MTD will be based on Cycle 1 (28 days).
Characterize the plasma pharmacokinetics (PK) of study drug and its metabolites.
Time frame: Safety will be characterized for the duration of time that each patient stays on study; estimated one year.
Assess the efficacy of study drug in terms of incidence of response rate and duration of response.
Time frame: All patients will remain on study until progression of disease, unacceptable toxicity, or another discontinuation criterion is met; estimated one year.
This study is completed, as verified in Sep 2020. You cannot join it, but the record below documents what was studied.
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Array Biopharma, now a wholly owned subsidiary of Pfizer