Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01316822 · ClinicalTrials.gov registry record · Phase 1

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

A Phase 1 study, sponsored by Array Biopharma, now a wholly owned subsidiary of Pfizer.

Completed
Registry status
Phase 1
Development phase
26
Enrollment target

NCT01316822: Completed Phase 1 study, sponsored by Array Biopharma, now a wholly owned subsidiary of Pfizer.

NCT01316822 is a Phase 1 study that has completed, run by Array Biopharma, now a wholly owned subsidiary of Pfizer. The registered enrollment target is 26 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (57% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01316822, a Phase 1 study, has completed, sponsored by Array Biopharma, now a wholly owned subsidiary of Pfizer.

COMPLETED
Registry status
Phase 1
Development phase
26 participants
Enrollment target

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.

Interventions

  • DRUG ARRY-382, cFMS inhibitor; oral

Trial Details

FieldValue
Enrollment Target 26 participants
Start Date 2011-03
Est. Completion 2012-10
Phase Phase 1

What the finished NCT01316822 record still lists

NCT01316822 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 26 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (57% lower).

The record links to 0 conditions, and to 1 intervention - of which ARRY-382, cFMS inhibitor; oral is the first listed.

NCT01316822 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01316822 about?

NCT01316822 is a clinical study titled "A Study of ARRY-382 in Patients With Selected Advanced or Metastatic Cancers". 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 fo...

What is the current status of trial NCT01316822?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 26 participants. The study started on 2011-03. Estimated completion is 2012-10.

What interventions are being tested in trial NCT01316822?

The interventions under investigation include: ARRY-382, cFMS inhibitor; oral (DRUG).

Who is sponsoring clinical trial NCT01316822?

This trial is sponsored by Array Biopharma, now a wholly owned subsidiary of Pfizer, which has 21 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01316822's enrollment target sits among peer trials

26 1482nd of 2000 higher than 506 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02646475 · 26 participants · Phase 1

    Metabolic Effects of Angiotensin-(1-7)

  • NCT03603223 · 26 participants · Phase 2

    Pembrolizumab in Treating Participants With Leukoplakia

  • NCT04063592 · 26 participants · NA

    AMI Construction in Lower Extremity Residual Limbs

  • NCT04906460 · 26 participants · Phase 1

    Open-label Study of WVE-N531 in Patients With Duchenne Muscular Dystrophy (FORWARD-53)

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01316822, the US trial registry maintained by the National Library of Medicine. NCT01316822 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.