Efficacy and Safety Clinical Trial
Official title:
Treatment of Non-responding to Conventional Therapy Inoperable Liver Cancers by in Situ Introduction of ImDendrim "[188Re]Rhenium Complex Coupled to an Imidazolic Ligand and Associated With a Dendrimer"
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.
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.
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