WHO ICTRP trial

An open-label study in patients with advanced cancer.

EUCTR2017-002243-15-GB · EU Clinical Trials Register · Authorised

Key facts

Trial ID EUCTR2017-002243-15-GB
Public title An open-label study in patients with advanced cancer.
Scientific title A Phase I/II Open-Label, Multi-center Study of the Safety and Efficacy of IMCnyeso, an HLA-A* 0201-Restricted, NY-ESO-1 and LAGE-1A-specific soluble T Cell Receptor and Anti-CD3 Bi-specific Molecule, as a Single Agent in HLA-A* 0201 Positive Patients With Advanced NY-ESO-1 and/or LAGE-1A Positive…
Primary sponsor Immunocore Ltd.
Registry EU Clinical Trials Register
Recruitment status Authorised
Study type Interventional clinical trial of medicinal product
Phase Human pharmacology (Phase I): yes Therapeutic exploratory (Phase II): yes Therapeutic confirmatory - (Phase III): no Therapeutic use (Phase IV): no
Countries United States;Canada;United Kingdom
Conditions HLA-A*0201 positive patients with advanced antigen-positive cancer with a histologic diagnosis of Non small cell lung carcinoma (NSCLC), melanoma, urothelial carcinoma, or synovial sarcoma with antigen positivity for NY-ESO-1 and/or LAGE-1A…
Interventions Product Name: IMCnyeso Product Code: IMCnyeso Pharmaceutical Form: Concentrate for solution for infusion INN or Proposed INN: IMCNYESO Current Sponsor code: IMCNYESO Concentration unit: mg/ml milligram(s)/millilitre Concentration type…
Registration date Apr 7, 2018
Target size 63
Secondary IDs IMCnyeso-101
Registry page clinicaltrialsregister.eu

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