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Parvovirus H-1 (ParvOryx) in Patients With Metastatic Inoperable Pancreatic Cancer — ParvOryx02  

Carcinoma, Pancreatic Ductal Clinical Trial

Official title:
A Non-controlled, Single Arm, Open Label, Phase II Study of Intravenous and Intratumoral Administration of ParvOryx in Patients With Metastatic, Inoperable Pancreatic Cancer

Clinical Trial Summary

Investigation on safety, tolerability and efficacy of parvovirus H-1 (ParvOryx) in subjects suffering from metastatic, inoperable pancreatic cancer with at least one hepatic metastasis.

Clinical Trial Description

Investigation on safety, tolerability and efficacy of parvovirus H-1 (ParvOryx) in subjects suffering from metastatic, inoperable pancreatic cancer with at least one hepatic metastasis. Initially four equal doses of ParvOryx will be administered intravenously on four consecutive days. Seven to fourteen days after the first intravenous administration the drug will be injected directly in a hepatic metastasis of the pancreatic cancer. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02653313
Study type Interventional
Source Oryx GmbH & Co. KG
Contact
Status Completed
Phase Phase 1/Phase 2
Start date December 2015
Completion date May 2018
View Details
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