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NCT02456701 · ClinicalTrials.gov registry record · Phase 1

Enhancing Radioiodine Incorporation Into BRAF Mutant Thyroid Cancers With the Combination of Vemurafenib and KTN3379

A Phase 1 study, sponsored by Celldex Therapeutics.

Completed
Registry status
Phase 1
Development phase
7
Enrollment target

NCT02456701: Completed Phase 1 study, sponsored by Celldex Therapeutics.

NCT02456701 is a Phase 1 study that has completed, run by Celldex Therapeutics. The registered enrollment target is 7 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (88% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02456701, a Phase 1 study, has completed, sponsored by Celldex Therapeutics.

COMPLETED
Registry status
Phase 1
Development phase
7 participants
Enrollment target

Study Summary

This is a patient pilot study testing the hypothesis that vemurafenib with the addition of KTN3379 can restore iodine incorporation in BRAF mutant (MUT), radioiodine-refractory (RAIR) thyroid cancer patients.

Interventions

  • DRUG vemurafenib
  • BIOLOGICAL KTN3379

Trial Details

FieldValue
Enrollment Target 7 participants
Start Date 2015-06
Est. Completion 2016-10-13
Phase Phase 1
Celldex Therapeutics

42 total trials

What the finished NCT02456701 record still lists

NCT02456701 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 7 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (88% lower).

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

NCT02456701 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02456701 about?

NCT02456701 is a clinical study titled "Enhancing Radioiodine Incorporation Into BRAF Mutant Thyroid Cancers With the Combination of Vemurafenib and KTN3379". This is a patient pilot study testing the hypothesis that vemurafenib with the addition of KTN3379 can restore iodine incorporation in BRAF mutant (MUT), radioiodine-refractory (RAIR) thyroid cancer patients.

What is the current status of trial NCT02456701?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 7 participants. The study started on 2015-06. Estimated completion is 2016-10-13.

What interventions are being tested in trial NCT02456701?

The interventions under investigation include: vemurafenib (DRUG), KTN3379 (BIOLOGICAL).

Who is sponsoring clinical trial NCT02456701?

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 NCT02456701's enrollment target sits among peer trials

7 1972nd of 2000 higher than 27 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 NCT02456701, the US trial registry maintained by the National Library of Medicine. NCT02456701 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.