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Brief Title: Parvovirus H-1 (ParvOryx) in Patients With Progressive Primary or Recurrent Glioblastoma Multiforme.
Official Title: Phase I/IIa Study of Intratumoral/Intracerebral or Intravenous/Intracerebral Administration of Parvovirus H-1 (ParvOryx) in Patients With Progressive Primary or Recurrent Glioblastoma Multiforme.
Study ID: NCT01301430
Brief Summary: Investigation on safety, tolerability and efficacy of H-1 parvovirus (H-1PV) in subjects suffering from glioblastoma multiforme.
Detailed Description: Investigation on safety, tolerability and efficacy of H-1 parvovirus (H-1PV) in subjects suffering from glioblastoma multiforme. H-1PV will primarily be administered either intratumoral or intravenously. Ten days thereafter a complete or a subtotal tumor resection with a subsequent administration of H-1PV into the walls of the resection cavity will be carried out.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Department of Neurosurgery, University Hospital Heidelberg, Heidelberg, , Germany
Name: Andreas Unterberg, Prof. Dr.
Affiliation: Department of Neurosurgery, University Hospital Heidelberg
Role: PRINCIPAL_INVESTIGATOR
Name: Bernard Huber, Dr.
Affiliation: Oryx GmbH & Co. KG
Role: STUDY_DIRECTOR