A Phase 3, Randomized, Double-blind, Placebo-controlled study to Determine the Efficacy and Safety of CMB305 in Unresectable Locally-advanced or Metastatic NY-ESO-1 + Synovial Sarcoma Subjects Following First-line Systemic Anti-cancer Therapy

×

Error message

  • Notice: Trying to access array offset on value of type null in bootstrap_pager() (line 53 of /var/www/biosafety.be/sites/all/themes/bootstrap/templates/system/pager.func.php).
  • Notice: Trying to access array offset on value of type null in bootstrap_pager() (line 95 of /var/www/biosafety.be/sites/all/themes/bootstrap/templates/system/pager.func.php).
Study title: 
A Phase 3, Randomized, Double-blind, Placebo-controlled study to Determine the Efficacy and Safety of CMB305 in Unresectable Locally-advanced or Metastatic NY-ESO-1 + Synovial Sarcoma Subjects Following First-line Systemic Anti-cancer Therapy
Long title: 
A Phase 3, Randomized, Double-blind, Placebo-controlled study to Determine the Efficacy and Safety of CMB305 in Unresectable Locally-advanced or Metastatic NY-ESO-1 + Synovial Sarcoma Subjects Following First-line Systemic Anti-cancer Therapy
Date receipt dossier: 
4 Oct 2018
EudraCT number: 
2018-000824-32
Company / Sponsor: 
Immune Design
Phase: 
III
Treated organism: 
Humans
Indication category: 
Cancer therapy
Disease: 
Synovial sarcomas
Therapeutic approach: 
Immunotherapy
Genetic modification: 
Replication deficient lentiviral vector encoding NY-ESO-1 cancer testis antigen
Method of transfer of nucleic acid of interest: 
not applicable
Administered biological material: 
Recombinant replication defective lentiviral vector (LV305)
Route of administration: 
Subcutaneous
Locations in Belgium: 
UZ Leuven
Type of procedure: 
Contained use only
Current status: 
Under evaluation