Xenotransplantation of Primary Cancer Samples in Zebrafish Embryos
NCT03668418 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 120
Last updated 2018-09-12
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
- Liver Cancer
- Pancreatic Cancer
- Gastric Cancer
- Esophageal Cancer
- Colo-rectal Cancer
- Gall Bladder Cancer
- Biliary Tract Cancer
Interventions
- DRUG
-
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
-
The enrolled patients after the surgical operation will undergo to the adjuvant chemotherapy treatment
- DRUG
-
The enrolled patients after the surgical operation will undergo to the adjuvant chemotherapy treatment
- DRUG
-
The enrolled patients after the surgical operation will undergo to the adjuvant chemotherapy treatment
- DRUG
-
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
-
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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