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NCT03829722 · ClinicalTrials.gov registry record · Phase 2

Radiotherapy, Carboplatin/Paclitaxel and Nivolumab for High Risk HPV-related Head and Neck Cancer

A Phase 2 study, sponsored by University of Michigan Rogel Cancer Center.

Completed
Registry status
Phase 2
Development phase
26
Enrollment target

NCT03829722: Completed Phase 2 study, sponsored by University of Michigan Rogel Cancer Center.

NCT03829722 is a Phase 2 study that has completed, run by University of Michigan Rogel Cancer Center. The registered enrollment target is 26 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (80% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03829722, a Phase 2 study, has completed, sponsored by University of Michigan Rogel Cancer Center.

COMPLETED
Registry status
Phase 2
Development phase
26 participants
Enrollment target

Study Summary

The purpose of this study is to find out if the addition of nivolumab can improve 2 year progression free survival (PFS) as compared to standard of care of fractionated radiation therapy (RT) and carboplatin/paclitaxel in subjects with high risk HPV-related squamous cell carcinoma of the oropharynx (tonsil, base of tongue, oropharyngeal wall, soft palate). Fractionated means the radiation will be administered in fragments or parts across multiple days.

Primary Outcome

Estimated using the Kaplan-Meier method. Evaluated using imaging and clinical exams

Interventions

  • DRUG Carboplatin
  • DRUG Nivolumab
  • DRUG Paclitaxel
  • RADIATION Radiation Therapy

Trial Details

FieldValue
Enrollment Target 26 participants
Start Date 2019-09-05
Est. Completion 2024-06-11
Phase Phase 2

What the finished NCT03829722 record still lists

NCT03829722 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 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (80% lower).

The record links to 0 conditions, and to 4 interventions - of which Carboplatin is the first listed.

NCT03829722 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03829722 about?

NCT03829722 is a clinical study titled "Radiotherapy, Carboplatin/Paclitaxel and Nivolumab for High Risk HPV-related Head and Neck Cancer". The purpose of this study is to find out if the addition of nivolumab can improve 2 year progression free survival (PFS) as compared to standard of care of fractionated radiation therapy (RT) and carboplatin/paclitaxel in subjects with high risk HPV-related squamous cell carcinoma of the oropharynx ...

What is the current status of trial NCT03829722?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 26 participants. The study started on 2019-09-05. Estimated completion is 2024-06-11.

What interventions are being tested in trial NCT03829722?

The interventions under investigation include: Carboplatin (DRUG), Nivolumab (DRUG), Paclitaxel (DRUG), Radiation Therapy (RADIATION).

Who is sponsoring clinical trial NCT03829722?

This trial is sponsored by University of Michigan Rogel Cancer Center, which has 292 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03829722's enrollment target sits among peer trials

26 1708th of 2000 higher than 282 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT03829722, the US trial registry maintained by the National Library of Medicine. NCT03829722 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.