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Trial to evaluate the safety and antitumor activity of FS222, a bispecific antibody against CD137/PD-L1, in subjects with advanced malignancies.
THE GOAL IS TO DETERMINE WHETHER FS222 IS SAFE IN THE TREATMENT OF CANCER AND THE DEGREE TO WHICH A PERSON TOLERATES THE SIDE EFFECTS.
- PHASE 1, OPEN-LABEL, FIRST-IN-HUMAN STUDY TO EVALUATE THE SAFETY AND ANTITUMOR ACTIVITY OF FS222, A BISPECIFIC ANTIBODY AGAINST CD137/PD-L1, IN SUBJECTS WITH ADVANCED MALIGNANCIES.
- Code EudraCT: -
- Protocol number: FS222-19101
- Promoter: F-star Beta Limited
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* The trials only admit a limited number of patients and are subject to inclusion and exclusion criteria. The specialist who assesses your case will inform you of the conditions required to participate in the clinical trial.
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Information offered by the Spanish Registry of Clinical Studies
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