Phase 1/2a Study of BAL101553 as 48-hour Infusions in Patients With Advanced Solid Tumors or Recurrent Glioblastoma

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

43

Participants

Timeline

Start Date

August 24, 2016

Primary Completion Date

August 7, 2020

Study Completion Date

August 7, 2020

Conditions
Neoplasms
Interventions
DRUG

BAL101553

BAL101553 48-hour infusion on day 1, 8, and 15 of each 28-day cycle; oral capsule daily for one week during Cycle 2 (study days 15-21)

DRUG

BAL101553 at MTD

BAL101553 48-hour infusion on day 1, 8, and 15 of each 28-day cycle; treatment with maximum tolerated dose (MTD)

Trial Locations (6)

1011

Centre Hospitalier Universitaire Vaudois, Lausanne

3010

Inselspital Bern, Bern

6500

Oncology Institute of Southern Switzerland; Ospedale Regionale San Giovanni Bellinzona e Valli, Bellinzona

7000

Cantonal Hospital of Grisons, Department of Oncology/ Haematology, Chur

8091

UniversitaetsSpital Zürich, Zurich

9007

Cantonal Hospital of St. Gallen, Dep. Medical Oncology & Hematology, Sankt Gallen

Sponsors
All Listed Sponsors
lead

Basilea Pharmaceutica

INDUSTRY