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NeuroblastomaNCT06851221

Β3-adrenoreceptor As Prognostic Marker in Neuroblastoma and Ewing Sarcoma

A study testing beta3 expression in people with Neuroblastoma and Ewing Sarcoma, run by Meyer Children's Hospital IRCCS at 1 site in Italy.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This study on biological samples of patients affected by neuroblastoma and Ewing sarcoma aims at validating the beta3-adrenoreceptor as prognostic biomarker. Read more about this study

Who is it for?
Ages 0 to 18 years
Conditions the study is for
Neuroblastoma, Ewing Sarcoma
What is being tested?
beta3 expression
Could I receive a placebo?
No, everyone receives an active treatment
How many people
95 participants
Where
1 siteItaly
Study dates
5 Aug 2020to 5 Mar 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 0 to 18 years
  • All sexes
  • No healthy volunteers
  • Child, Adult

Who may be able to join

  • diagnosis of Ewing sarcoma or neuroblastoma

Who cannot join

  • sieropositivity

Trial locations and contacts

1 site in 1 country.

Italy1 site
  • Laboratorio traslazionale in oncoematologia

    Florence, Italy, 50139

Other trials in Italy

About this study

This study on biological samples of patients affected by neuroblastoma and Ewing sarcoma aims at validating the beta3-adrenoreceptor as prognostic biomarker.

Being tested
beta3 expression
Medical subject headings
Neuroblastoma, Sarcoma, Ewing

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • beta3 expressionDiagnostic test

    the samples leftover from the standard diagnostic procedures will be analyzed for the expression of the beta3-adrenoreceptor

Study groups in NCT06851221
Study groupRoleWhat they receive
biological samples analysisOtherNot described
Receives: Diagnostic Test: beta3 expression

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. expression of beta3-adrenoreceptor

    Measured: from enrollment to the performance of the analysis that can take up to 6 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Feb 2025
  2. Study start5 Aug 2020
  3. Primary completion5 Mar 2024
  4. Study completion5 Mar 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
95 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06851221
Sponsor's protocol ID
BETA3TumPed
Status last verified
Feb 2025
First submitted
21 Feb 2025
Last updated
28 Feb 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing beta3 expression in people with Neuroblastoma and Ewing Sarcoma, run by Meyer Children's Hospital IRCCS at 1 site in Italy.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 28 Feb 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

expression of beta3-adrenoreceptor (time frame: from enrollment to the performance of the analysis that can take up to 6 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Feb 2025.

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