Xenotransplantation of Primary Cancer Samples in Zebrafish Embryos

NCT03668418 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 120

Last updated 2018-09-12

No results posted yet for this study

Summary

The study consists in a co-clinical trial by using zebrafish embryos. Specifically, an observational prospective clinical trial on patients operated of epato-biliar-pancreatic cancers and gastro-intestinal cancers undergoing a chemotherapy treatment will be run concurrently to an animal trial on zebrafish embryos xenotransplanted with patient cancer cells in order to demonstrate that zebrafish model is able to predict the therapeutic regimen with the best efficacy for each patient.

Conditions

Interventions

DRUG

Fluorouracil

The enrolled patients after the surgical operation will undergo to the adjuvant chemotherapy treatment

DRUG

Lederfolin

The enrolled patients after the surgical operation will undergo to the adjuvant chemotherapy treatment

DRUG

Oxaliplatin

The enrolled patients after the surgical operation will undergo to the adjuvant chemotherapy treatment

DRUG

Irinotecan

The enrolled patients after the surgical operation will undergo to the adjuvant chemotherapy treatment

DRUG

Docetaxel

The enrolled patients after the surgical operation will undergo to the adjuvant chemotherapy treatment

DRUG

Cisplatin

The enrolled patients after the surgical operation will undergo to the adjuvant chemotherapy treatment

DRUG

Epirubicin

The enrolled patients after the surgical operation will undergo to the adjuvant chemotherapy treatment

DRUG

Gemcitabine

The enrolled patients after the surgical operation will undergo to the adjuvant chemotherapy treatment

DRUG

Nab paclitaxel

The enrolled patients after the surgical operation will undergo to the adjuvant chemotherapy treatment

Sponsors & Collaborators

  • Azienda Ospedaliero, Universitaria Pisana

    collaborator OTHER
  • University of Pisa

    lead OTHER

Principal Investigators

  • Luca Morelli, Prof · University of Pisa

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-06-01
Primary Completion
2021-05-31
Completion
2022-05-31
FDA Drug
Yes

Countries

  • Italy

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03668418 on ClinicalTrials.gov