Safety, Tolerability and Pharmacokinetics of Oral CPL304110, in Adult Subjects With Advanced Solid Malignancies

PHASE1RecruitingINTERVENTIONAL
Enrollment

42

Participants

Timeline

Start Date

July 19, 2019

Primary Completion Date

June 30, 2024

Study Completion Date

June 30, 2024

Conditions
Gastric CancerBladder CancerSquamous Non-small Cell Lung CancerCholangiocarcinomaSarcomaEndometrial CancerOther Solid Tumours
Interventions
DRUG

CPL304110

CPL304110 is to be administered orally as hard gelatine capsules once daily in 28-day cycles.

Trial Locations (7)

Unknown

RECRUITING

Uniwersyteckie Centrum Kliniczne w Gdańsku, Gdansk

RECRUITING

BioResearch Group sp. z o.o., Nadarzyn

RECRUITING

SP ZOZ MSWiA z Warmińsko-Mazurskim Centrum Onkologii w Olsztynie, Olsztyn

NOT_YET_RECRUITING

Klinika Onkologii, Europejskie Centrum Zdrowia, Otwock

RECRUITING

Centrum Onkologii - Instytut im. Marii Skłodowskiej-Curie, Warsaw

RECRUITING

Instytut Gruźlicy i Chorób Płuc, Warsaw

NOT_YET_RECRUITING

Wojskowy Instytut Medyczny, Warsaw

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

National Center for Research and Development, Poland

OTHER

lead

Celon Pharma SA

INDUSTRY