drugset / Trial / NCT07307053

Rare Tumor Focused Platform Study of Innovative Therapies and Technologies (PLATFORM2)

NCT07307053

Phase 1/2 Not yet recruiting 600 enrolled Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The goal of this Phase I/II observational and interventional platform study is to evaluate the safety and efficacy of multiple types of innovative anti-tumor drugs and new technologies in patients with rare solid tumors. The study utilizes multi-dimensional precision screening (including WES, RNAseq, mIHC, and quantitative proteomics) to match patients with specific sub-protocols. Key questions it aims to answer: Assess the safety of innovative therapies in rare tumor populations. Evaluate the objective response rate (ORR) and other efficacy metrics. Explore biomarkers related to therapeutic efficacy. Participants: Patients with metastatic or advanced rare solid tumors who have failed standard therapy or have no standard treatment options.

Timeline

Start
2026-01-01
Primary completion
2029-01-31
Completion
2031-01-31

Drugs

EvaluationDrugModalityDoseRoute
Subject BMD006 Messenger RNA (mRNA) Inhaled
Subject CE120 Other / unclassified Other
Subject CREPT-618 Oligonucleotide (other)
Subject CVL006 Monoclonal antibody
Subject GV20-0251 Monoclonal antibody
Subject IBI363 Protein / enzyme biologic
Subject IDOV-SAFE Unknown
Subject Izalontamab Brengitecan Unknown
Subject KXV01 Cell therapy Intravenous
Subject LYC001 Protein / enzyme biologic
Subject MT027 Cell therapy Other
Subject Metabolically Armed TIL cells Cell therapy Intravenous
Subject NK510 Cell therapy
Subject PRG2505 Cell therapy
Subject QH101 Cell therapy Intrathecal
Subject TAEST1901 Cell therapy Intravenous
Subject TC-N201 Cell therapy
Subject VSV Unknown
Subject YL201 Other / unclassified
Subject YSCH-01 Unknown