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Spots Global Cancer Trial Database for Parvovirus H-1 (ParvOryx) in Patients With Progressive Primary or Recurrent Glioblastoma Multiforme.

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Trial Identification

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

Interventions

H-1PV

Study Description

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.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Department of Neurosurgery, University Hospital Heidelberg, Heidelberg, , Germany

Contact Details

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

Useful links and downloads for this trial

Clinicaltrials.gov

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