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Trial · NCT04464122

Rediscovering Biomarkers for the Diagnosis and Early Treatment Response in NEN (REBORN)

NCT04464122, Recruiting, University of Roma La Sapienza

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Rediscovering Biomarkers for the Diagnosis and Early Treatment Response in NEN (REBORN). Trials, record NCT04464122. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04464122

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Rediscovering Biomarkers for the Diagnosis and Early Treatment Response in NEN (REBORN)
NCT number
NCT04464122
Status
Recruiting
Enrollment
60 participants, estimated
Lead sponsor
University of Roma La Sapienza
Conditions
Neuroendocrine Tumors, Neuroendocrine Neoplasm, Neuroendocrine Tumor Grade 1, Neuroendocrine Tumor Grade 2, Neuroendocrine Carcinoma
Interventions
Somatostatin analog; chemotherapy
First posted
2020-07-09
Last updated
2025-04-03

Source ClinicalTrials.gov

Registered outcomes13

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryTo evaluate the modification of the angiogenetic mediator sTie2 after treatment.baseline - + 1 month - +3 monthsModification of sTie (soluble Tie2) after treatment
SecondaryTo evaluate the difference in the angiogenetic mediator sTie2 between patients and controlsbaselineComparison of basal levels of sTie between patients and controls
SecondaryTo validate the use of circular RNAs from TEPs in NEN diagnosisbaselineValidation of the use of circular RNAs sequencing from tumor educated platelets (TEPs) in NETs diagnosis, through the comparison between patients and controls
SecondaryTo evaluate the changing in circular RNAs from TEPs in NEN patients after somatostatin analogs treatmentbaseline - + 1 month - +3 monthsModification in circular RNAs sequencing from tumor educated platelets (TEPs) in patients after treatment
SecondaryTo compare circular and cellular angiogenesis mediators between patients and controlsbaseline
Comparison of basal level of other circular and cellular angiogenesis mediators between patients and controls (Angiogenic factors: ANG1, ANG2, FGF1, FGF2, NRP1, NRP2, VEGFA, VEGFB, VEGFC, HIF1A, NOS3, PROK1, PROK2; Cytokines: CCL11, CCL2, CXCL1, CXCL10, CXCL5, CXCL6, CXCL9, IL1B, IL6, TNF; Receptors and other angiogenic factors: VEGFR1, VEGFR2, TIE2, PDGFR, TGFBR, MMP14, MMP2, MMp9, TIMP1, TIMP2, TIMP3, PROKR1, PROKR2)
SecondaryTo evaluate the changing in circular and cellular angiogenesis mediators after treatment.baseline - + 1 month - +3 months
Modification of other circular and cellular angiogenesis mediators in patients after treatment (Angiogenic factors: ANG1, ANG2, FGF1, FGF2, NRP1, NRP2, VEGFA, VEGFB, VEGFC, HIF1A, NOS3, PROK1, PROK2; Cytokines: CCL11, CCL2, CXCL1, CXCL10, CXCL5, CXCL6, CXCL9, IL1B, IL6, TNF; Receptors and other angiogenic factors: VEGFR1, VEGFR2, TIE2, PDGFR, TGFBR, MMP14, MMP2, MMp9, TIMP1, TIMP2, TIMP3, PROKR1, PROKR2)
SecondaryTo quantify PBMC subpopulation in patients and controlsbaselineQuatification of peripheral blood mononuclear cells (PBMC) subpopulations in patients and controls
SecondaryTo evaluate the modification of PBMC subpopulation in patients after treatmentbaseline - + 1 month - +3 monthsModification of peripheral blood mononuclear cells (PBMC) subpopulations in patients after treatment
SecondaryTo compare classical neuroendocrine markers serum levels between patients and controlsbaselineComparison of basal serum level of classical neuroendocrine markers (chromogranin a and neuron specific enolase) between patients and controls
SecondaryTo evaluate the modification of classical neuroendocrine markers in patients after treatmentbaseline - + 1 month - +3 monthsModification of classical neuroendocrine markers (chromogranin a and neuron specific enolase) in patients after treatment

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers6

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
11448916BACKGROUNDPubMed
17045842BACKGROUNDPubMed
20633984BACKGROUNDPubMed
26525104BACKGROUNDPubMed
26555171BACKGROUNDPubMed
28681241BACKGROUNDPubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT04464122

GET https://conductscience.org/api/trials/v1/NCT04464122/registered