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Spots Global Cancer Trial Database for Study of the AL3810 in the Treatment of Advanced Solid Tumor

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Trial Identification

Brief Title: Study of the AL3810 in the Treatment of Advanced Solid Tumor

Official Title: An Open-label, Dose-finding Phase I Study to Determine the Maximum Tolerated Dose, Recommended Dose, Pharmacokinetics, Pharmacodynamics of the Dual -VEGFR-FGFR Tyrosine Kinase Inhibitor, AL3810, Givenorally as Single Agent to Patients With Advanced Solid Tumours

Study ID: NCT03117101

Interventions

Lucitanib

Study Description

Brief Summary: This was a monocentric, open label, non-randomised, non-comparative, dose-finding phase I study

Detailed Description: Methodology: This was a monocentric, open label, non-randomised, non-comparative, dose-finding phase I study with a traditional 3+3 design, conducted in Chinese patients with advanced solid tumours without an established therapeutic alternative.This study was performed in strict accordance with Good Clinical Practice including the archiving of essential documents.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Fudan University Shanghai Cancer Center, Shanghai, Shanghai, China

Contact Details

Name: Jin Li, M.D.

Affiliation: Fudan University

Role: PRINCIPAL_INVESTIGATOR

Name: Junning Cao, M.D.

Affiliation: Fudan University

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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