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Clinical Trial Summary

The purpose of the study is to determine to evaluate safety and tolerability of CPL304110 when administered once daily to adults with advanced solid malignancies.


Clinical Trial Description

01FGFR2018 is an Open-label, Multicentre, Dose Escalation Study to Assess Safety, Tolerability and Pharmacokinetics of Oral CPL304110, in Adult Subjects with Advanced Solid Malignancies. The study consists of 3 parts: initial dose escalation (Part 1 - without FGFR, fibroblast growth factor receptor, molecular aberrations), dose escalation (Part 2 - with FGFR molecular aberrations) and dose extension (Part 3 - with FGFR molecular aberrations). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04149691
Study type Interventional
Source Celon Pharma SA
Contact CROS CRO
Phone +48 791 690 990
Email clinicaltrials@cros-cro.com
Status Recruiting
Phase Phase 1
Start date July 19, 2019
Completion date June 2024

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