NCT04471987

Safety and Early Signs of Efficacy of IL12-L19L19.

← 임상시험 허브

레지스트리 요약

진행 상태
모집중 (RECRUITING)
질환/조건
Advanced Solid Tumor, Metastatic Solid Tumor
시험 유형
중재 연구 (INTERVENTIONAL)
단계
Phase 1
목적
치료
중재 유형
약물
개입·치료
IL12-L19L19, IL12-L19L19
Lead Sponsor
Philogen S.p.A. (산업계)

캐시 시각: 2026-09-10 23:27:12

ClinicalTrials.gov에서 보기

요약

The purpose of this study is to describe the safety, tolerability and early signs of efficacy of the antibody-cytokine fusion protein IL12-L19L19 in patients with advanced or metastatic solid carcinomas, after previous immune checkpoint blockade therapy.

The primary objective of the study is to evaluate the safety of IL12-L19L19 and to establish MTD in order to establish a recommended dose (RD).

The secondary objectives of the study are to assess early signs of efficacy, the determination of pharmacokinetic (PK) properties and the immunogenicity of IL12-L19L19.

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