Study title:
A phase II study evaluating the efficacy and the safety of first-line chemotherapy combined with TG4010 and nivolumab in patients with advanced non-squamous Non-Small-Cell Lung Cancer (NSCLC)
EU record number:
B/BE/17/BVW1
EudraCT number:
2016-005115-41
Company / Sponsor:
Transgene
Treated organism:
Humans
Indication category:
Cancer therapy
Disease:
Use as a chemotherapy in combination with the monoclonal antibody Nivolumab in patients with advanced non-squamous Non-Small-Cell Lung Cancer (NSCLC)
Genetic modification:
Sequences coding for human mucine 1 (MUC1) antigen and interleukin-2 (IL2)
Method of transfer of nucleic acid of interest:
Attenuated Vaccinia Virus (Ankara Strain)
Route of administration:
Subcutaneous
Locations in Belgium:
Centre Hospitalier de l’Ardenne, Libramont
Nr of subjects:
5 patients foreseen in Belgium
Foreseen duration:
2 years
Type of procedure:
Contained use and Deliberate release
Information for the public
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Public information presented according to the provisions of Directive 2001/18/EC
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Information related to the decision procedure
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5 September 2017 - The Biosafety Council issues a positive advice (with conditions) for this trial
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28 November 2017: The Federal Ministers give a final decision (positive) for this trial