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A Study to Evaluate the Safety of LAM561 Added to Standard of Care in Newly-diagnosed Glioblastoma Patients

NCT03867123 PHASE1 COMPLETED

The purpose of this study is to determine the safety and tolerability of LAM561 added to first-line treatment for subjects with newly diagnosed glioblastoma (GBM), and to determine the highest safe dose of LAM561 administered orally when added to the concurrent phase of treatment with temozolomide (TMZ) and radiation therapy (RT) or when added to the maintenance phase of treatment with TMZ (once TMZ 200 g/m2/day is started).

Details

Lead sponsorLaminar Pharmaceuticals
PhasePHASE1
StatusCOMPLETED
Enrolment18
Start dateTue Dec 04 2018 00:00:00 GMT+0000 (Coordinated Universal Time)
CompletionWed Jul 01 2020 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

Interventions

Countries

Spain