Actively Recruiting

Age: 0Years +
All Genders
NCT05024929

Targeted Therapy to Increase RAI Uptake in Metastatic DTC

Led by Children's Hospital of Philadelphia · Updated on 2025-11-14

32

Participants Needed

9

Research Sites

602 weeks

Total Duration

On this page

Sponsors

C

Children's Hospital of Philadelphia

Lead Sponsor

U

United States Department of Defense

Collaborating Sponsor

AI-Summary

What this Trial Is About

Papillary thyroid cancer (PTC) is a common type of differentiated thyroid cancer (DTC) in children and represents the second most common cancer in adolescent females. Recently targeted drugs that block many of the genetic drivers of DTC have become available. While Investigators know that these drugs shrink DTC tumors in many cases, the impact on radioactive iodine (RAI) avidity has not been systematically studied.

CONDITIONS

Official Title

Targeted Therapy to Increase RAI Uptake in Metastatic DTC

Who Can Participate

Age: 0Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with a histologic diagnosis of differentiated thyroid cancer
  • Presence of targetable genetic alterations such as NTRK-fusion, RET-fusion, ALK-fusion, BRAF V600 mutation, or BRAF-fusion identified in a certified laboratory
  • Anatomically evaluable lung metastases on chest CT within 180 days before enrollment, including multiple (10 or more) noncalcified solid pulmonary nodules or enlarging discrete pulmonary nodules consistent with metastatic disease
  • Planned systemic therapy with an oncogene-specific kinase inhibitor from commercial supply or as part of a separate therapeutic trial, compassionate use, or single patient IND
  • Patients enrolled on other oncogene-specific targeted therapy trials who have whole body thyroid scans about 28 days after starting therapy and agree to data sharing
Not Eligible

You will not qualify if you...

  • Prior oncogene-specific targeted therapy is not allowed, except enrollment within 4 weeks of starting therapy if a pre-therapy whole body scan is available
  • Females who are pregnant or breastfeeding
  • Patients requiring sedation or general anesthesia to complete a whole body scan
  • U.S. Military personnel are excluded due to institutional review board requirements

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 9 locations

1

University of California San Francisco

San Francisco, California, United States, 94143

Actively Recruiting

2

Emory University School of Medicine

Atlanta, Georgia, United States, 30322

Actively Recruiting

3

Boston Children's Hospital

Boston, Massachusetts, United States, 02115

Actively Recruiting

4

Children's Hospital of Philadelphia

Philadelphia, Pennsylvania, United States, 19104

Actively Recruiting

5

St. Jude Children's Research Hospital

Memphis, Tennessee, United States, 38105

Actively Recruiting

6

MD Anderson Cancer Center

Houston, Texas, United States, 77030

Actively Recruiting

7

Texas Children's Hospital

Houston, Texas, United States, 77030

Actively Recruiting

8

Seattle Children's Hospital

Seattle, Washington, United States, 98105

Actively Recruiting

9

Children's Hospital Westmead

Sydney, New South Wales, Australia

Actively Recruiting

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Research Team

M

Meghan T Donnelly

CONTACT

J

James Robinson

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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