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Clinical Trial Summary

Objective (s) : To Evaluate the efficacy and safety of Treatment of non-responding to conventional therapy inoperable liver cancers by in situ introduction of ImDendrim.

Trial Design:

An, open-labeled and unicenter study in women or men with primary hepatocellular cancer or metastatic liver without standard therapeutic options for treatment including chemotherapy or surgery.


Clinical Trial Description

Objective (s) : To Evaluate the efficacy and safety of Treatment of non-responding to conventional therapy inoperable liver cancers by in situ introduction of ImDendrim "[188Re] rhenium complex coupled to a imidazolic ligand and associated with a dendrimer".

Trial Design:

1. Type of the clinical Trial:

An, open-labeled and unicenter study in women or men with primary hepatocellular cancer or metastatic liver without standard therapeutic options for treatment including chemotherapy or surgery.

2. Duration and method The trial will be comprised of 12 weeks of continued observation following in situ injection of ImDendrim into a subject suffering non-responding to conventional therapy inoperable liver cancers. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03255343
Study type Interventional
Source French Association for the Advancement Medical Research
Contact HAFID BELHADJ-TAHAR, MD, PhD
Phone 00336467722224
Email belhadj-tahar@afpremed.org
Status Recruiting
Phase N/A
Start date March 13, 2017
Completion date December 31, 2017

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