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CompletedNCT01316822Updated Sep 21, 2020

A Study of ARRY-382 in Patients With Selected Advanced or Metastatic Cancers

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

Phase
Phase 1
Study type
Interventional
Enrollment
26
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

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.

02

Conditions studied

  • Metastatic Cancer

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Keywords

  • CSF1R
  • M-CSF
  • CSF-1
  • c-FMS
  • Tumor-associated macrophage
  • Macrophage-Colony Stimulating Factor-1
  • Receptor tyrosine kinase inhibitor
  • Tumor cell-induced osteolysis
03

In context

Neoplasm Metastasis

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 →

Lead sponsor

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.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Key Inclusion Criteria:

  • A histologically or cytologically confirmed diagnosis of advanced or metastatic solid cancer refractory to standard treatment, for which no standard therapy is available or for which the patient refuses standard therapy.
  • Measurable disease or evaluable, nonmeasurable disease.
  • Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0, 1 or 2.
  • Hemoglobin ≥ 9.0 g/dL, ANC > 1500/uL and platelet count ≥ 100,000/uL.
  • AST/serum glutamic oxaloacetic transaminase (SGOT) and ALT/serum glutamic pyruvic transaminase (SGPT) ≤ 2.5 × the upper limit of normal (ULN).
  • Bilirubin ≤ ULN.
  • Serum creatinine ≤ 1.5 × ULN.
  • Potassium, magnesium and calcium (corrected calcium when serum albumin levels are abnormal) within the normal range.
  • Additional criteria exist.

Key Exclusion Criteria:

  • 12-lead ECG demonstrating a mean QTcF > 450 msec (triplicate assessment) at the Screening Visit or history/evidence of long QT syndrome.
  • History of acute coronary syndromes, including unstable angina, coronary angioplasty, or stenting, within the past 24 weeks.
  • Use of concomitant medications that prolong the QT/QTc interval, as assessed by the Investigator, within 14 days prior to first dose of study drug.
  • Use of concomitant medication that is a strong CYP3A inhibitor or inducer within 14 days prior to first dose of study drug.
  • Class II, III or IV heart failure as defined by the New York Heart Association (NYHA) functional classification system.
  • Uncontrolled or symptomatic brain metastases (if a patient has brain metastases and is on steroids, the steroid dose must have been stable for at least 30 days).
  • Active refractory nausea and vomiting, chronic gastrointestinal diseases (e.g., inflammatory bowel disease) or significant bowel resection that, in the judgment of the Investigator, would preclude adequate absorption (a previous Whipple procedure is allowed).
  • Additional criteria exist.
05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
26 participants (actual)

Study arms

  • Experimental
    ARRY-382

    Drug: ARRY-382, cFMS inhibitor; oral

Interventions

  • DrugARRY-382, cFMS inhibitor; oral

    multiple dose, escalating

06

What researchers measure

Primary outcomes

  1. 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.

  2. Establish the maximum tolerated dose (MTD) of study drug.

    Time frame: The MTD will be based on Cycle 1 (28 days).

  3. 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.

Secondary outcomes

  1. 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.

07

Study locations

2 sites
  • Sarah Cannon Research Institute
    Nashville, Tennessee 37203, United States
  • South Texas Accelerated Research Therapeutics (START)
    San Antonio, Texas 78229, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 21, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01316822
Lead sponsor
Array Biopharma, now a wholly owned subsidiary of Pfizer
Responsible party
Sponsor
First posted
Mar 16, 2011
Start date
Mar 2011
Primary completion
Oct 2012
Completion
Oct 2012
Last update
Sep 21, 2020

Study contacts

Pfizer CT.gov Call Center
study director · Pfizer
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

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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