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NCT03667482 · ClinicalTrials.gov registry record · Phase 1

Cabozantinib in Combination With Cetuximab in Patients With Recurrent or Metastatic Head and Neck Squamous Cell Cancer

A Phase 1 study, sponsored by Memorial Sloan Kettering Cancer Center.

Completed
Registry status
Phase 1
Development phase
20
Enrollment target

NCT03667482: Completed Phase 1 study, sponsored by Memorial Sloan Kettering Cancer Center.

NCT03667482 is a Phase 1 study that has completed, run by Memorial Sloan Kettering Cancer Center. The registered enrollment target is 20 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT03667482, a Phase 1 study, has completed, sponsored by Memorial Sloan Kettering Cancer Center.

COMPLETED
Registry status
Phase 1
Development phase
20 participants
Enrollment target

Study Summary

The purpose of this study is to test the safety of cabozantinib, at different doses, in combination with cetuximab to find out what effects, if any, this combined treatment has on people with HNSCC.

Primary Outcome

from 3 testing dose levels: 20, 40, and 60. Three patients will be enrolled at the dose level 0 of 40 mg. The dose escalation scheme is as follows: 1. If none of the initial three patients at a given dose level experience DLT within 4 weeks, the next dose level will be studied. 2. If one of the initial three patients at a given dose level experiences DLT, three additional patients will be treated at the same dose level. Escalation will continue only if there is no additional DLT observed.If two

Interventions

  • DRUG Cetuximab
  • DRUG Cabozantinib

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2018-09-07
Est. Completion 2024-07-17
Phase Phase 1
Memorial Sloan Kettering Cancer Center

1,884 total trials

What the finished NCT03667482 record still lists

NCT03667482 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% lower).

The record links to 0 conditions, and to 2 interventions - of which Cetuximab is the first listed.

NCT03667482 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03667482 about?

NCT03667482 is a clinical study titled "Cabozantinib in Combination With Cetuximab in Patients With Recurrent or Metastatic Head and Neck Squamous Cell Cancer". The purpose of this study is to test the safety of cabozantinib, at different doses, in combination with cetuximab to find out what effects, if any, this combined treatment has on people with HNSCC.

What is the current status of trial NCT03667482?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 20 participants. The study started on 2018-09-07. Estimated completion is 2024-07-17.

What interventions are being tested in trial NCT03667482?

The interventions under investigation include: Cetuximab (DRUG), Cabozantinib (DRUG).

Who is sponsoring clinical trial NCT03667482?

This trial is sponsored by Memorial Sloan Kettering Cancer Center, which has 1,884 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03667482's enrollment target sits among peer trials

20 1629th of 2000 higher than 285 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

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Source: ClinicalTrials.gov NCT03667482, the US trial registry maintained by the National Library of Medicine. NCT03667482 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.