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NCT06423950Recruiting

Generating Novel Translational and Therapeutic Strategies Based on a Multicenter, Pediatric and AYA Evolutionary Tumor Board (pedsETB)

Feasibility of Generating Novel Translational and Therapeutic Strategies Based on a Multicenter, Pediatric and AYA Evolutionary Tumor Board (pedsETB)

Source: ClinicalTrials.gov · Last updated 21 Sept 2026

Brief summary (registry, in English)

To evaluate the ability of a multidisciplinary and multisite group, the Pediatric Evolutionary Tumor Board (pedsETB), to develop additional therapeutic strategies in patients without curative options or with suboptimal outcomes.

Status (registry)
Recruiting
Study type
Observational
Enrollment
35 (estimated)
First submitted
9 May 2024
Start date
May 2024
Primary completion date
Apr 2027
Lead sponsor
H. Lee Moffitt Cancer Center and Research Institute
NCT number
NCT06423950

What you commit to

  • Study type: Observational
  • Planned participants: 35
  • From May 2024 to the primary completion date, Apr 2027
  • 5 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Participants without known therapies to reliably induce a response are excluded from pedsETB and should seek clinical trials.

Who the study is looking for

  • Participant must be considered likely incurable given the standard of care. This is inclusive of patients newly diagnosed, relapsed or in remission but at high risk of recurrence, with suboptimal responses to previous therapy, or with many potentially beneficial, but unlikely curative options for care.
    • The site investigator will make this determination based on their experience.
  • Participant must have an age-appropriate performance status: Karnofsky 50 or more for patients 16 years of age or older OR Lansky score of 50 or more for patients less than16 years of age.
  • Participant and/or parents or legal guardian and primary oncologist must be willing to consider the therapeutic strategies recommended by the pedsETB.
  • Participant must be willing to be followed over time and allow collection of clinical data including scans, available blood and lab samples, and optional pedsETB serial blood sampling.
  • All Participants and/or their parents or legal guardians must have the ability to understand and the willingness to sign a written informed consent or assent document.

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (5)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Roswell Park Comprehensive Cancer Center
Coordinator of this site? Confirm its status
BuffaloUnited StatesRecruiting
Connecticut Children's Medical Center
Coordinator of this site? Confirm its status
HartfordUnited StatesRecruiting
University of Kentucky
Coordinator of this site? Confirm its status
LexingtonUnited StatesRecruiting
University of Miami
Coordinator of this site? Confirm its status
MiamiUnited StatesRecruiting
Moffitt Cancer Center
Coordinator of this site? Confirm its status
TampaUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.