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NCT03254927 · ClinicalTrials.gov registry record · Phase 2

A Study of CDX-3379 and Cetuximab and in Patients With Advanced Head and Neck Squamous Cell Carcinoma

A Phase 2 study, sponsored by Celldex Therapeutics.

Terminated
Registry status
Phase 2
Development phase
30
Enrollment target

NCT03254927: Clinical Trial Phase 2 study, sponsored by Celldex Therapeutics.

NCT03254927 is a Phase 2 study that was terminated before completion, run by Celldex Therapeutics. The registered enrollment target is 30 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (77% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03254927, a Phase 2 study, was terminated before completion, sponsored by Celldex Therapeutics.

TERMINATED
Registry status
Phase 2
Development phase
30 participants
Enrollment target

Study Summary

This is a study to determine the clinical benefit (how well the drug works), safety and tolerability of combining CDX-3379 and cetuximab. The study will enroll patients with advanced head and neck squamous cell carcinoma who have previously received cetuximab and progressed.

Primary Outcome

The percentage of patients who achieve a complete response or partial response per Per Response Evaluation Criteria In Solid Tumors Criteria (RECIST version 1.1), Complete Response (CR) = disappearance of all target lesions and non-target lesions, Partial Response (PR), \>= 30% decrease in the sum of the longest diameter of target lesions with no progression in non-target lesions and no new lesions.

Interventions

  • DRUG CDX-3379 and cetuximab

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2018-03-27
Est. Completion 2020-12-16
Phase Phase 2
Celldex Therapeutics

42 total trials

Why NCT03254927 stopped before completion

NCT03254927 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (77% lower).

The record links to 0 conditions, and to 1 intervention - of which CDX-3379 and cetuximab is the first listed.

NCT03254927 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03254927 about?

NCT03254927 is a clinical study titled "A Study of CDX-3379 and Cetuximab and in Patients With Advanced Head and Neck Squamous Cell Carcinoma". This is a study to determine the clinical benefit (how well the drug works), safety and tolerability of combining CDX-3379 and cetuximab. The study will enroll patients with advanced head and neck squamous cell carcinoma who have previously received cetuximab and progressed.

What is the current status of trial NCT03254927?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 30 participants. The study started on 2018-03-27. Estimated completion is 2020-12-16.

What interventions are being tested in trial NCT03254927?

The interventions under investigation include: CDX-3379 and cetuximab (DRUG).

Who is sponsoring clinical trial NCT03254927?

This trial is sponsored by Celldex Therapeutics, which has 42 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03254927's enrollment target sits among peer trials

30 1582nd of 2000 higher than 332 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 NCT03254927, the US trial registry maintained by the National Library of Medicine. NCT03254927 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.