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Clinical trial to evaluate the safety of GEN1053 in monotherapy and in combination with an immunomodulator in patients with malignant solid tumors

THE PRIMARY OBJECTIVE OF THE DOSE ESCALATION PORTION OF THIS TRIAL IS TO DETERMINE THE HIGHEST TOLERATED AND SAFEST DOSE THAT CAN BE ADMINISTERED TO CANCER PATIENTS

Status
In recruitment
headquarters
Pamplona

Technical Summary

* 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.

More information about this clinical trial

Information offered by the Spanish Registry of Clinical Studies

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