Berubicin in Adult Patients With Recurrent Glioblastoma Multiforme (WHO Grade IV)

PHASE1/PHASE2TerminatedINTERVENTIONAL
Enrollment

5

Participants

Timeline

Start Date

December 7, 2022

Primary Completion Date

December 30, 2023

Study Completion Date

December 30, 2023

Conditions
Recurrent Glioblastoma Multiforme
Interventions
DRUG

Berubicin Hydrochloride

Berubicin intravenously infused will be administered at a dose of 7.1 mg/m2 as free base (equivalent to 7.5 mg/m2 Berubicin HCl) as a 2-hour intravenous (IV) infusion once daily for 3 consecutive days followed by 18 days off study drug (each cycle = 21 days).

Trial Locations (2)

80-214

Uniwersyteckie Centrum Kliniczne Klinika Onkoligii i Radioterapii, Gdansk

02-781

Narodowy Instytut Onkologii im. Marii Skłodowskiej-Curie,Państwowy Instytut Badawczy w Warszawie,Klinika Nowotworów Głowy i Szyi, Warsaw

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Worldwide Clinical Trials

OTHER

collaborator

National Center for Research and Development, Poland

OTHER

lead

WPD Pharmaceuticals Sp. z o.o.

INDUSTRY