Phase I Study of Autologous Tumor-Draining Lymph Node-Derived Lymphocytes for Advanced HER2-Negative Breast Cancer - Trial NCT06121557
Access comprehensive clinical trial information for NCT06121557 through Pure Global AI's free database. This Phase 1 trial is sponsored by Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University and is currently Recruiting. The study focuses on Breast Neoplasms. Target enrollment is 24 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.
Study Focus
Sponsor & Location
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Timeline & Enrollment
Phase 1
Nov 01, 2023
Dec 31, 2031
Primary Outcome
Incidence of Dose-Limiting Toxicity (DLT),Incidence of Grade≥3 Treatment-Emergent Adverse Event (TEAE)
Summary
RATIONALE: Patients with HER2-negative advanced breast cancer have limited choice on targeted
 therapies, and often show only modest responses to available immunotherapies. Adoptive cell
 therapy with tumor-infiltrating lymphocytes has difficulties in preparing enough cells from
 solid tumors and overcoming the exhaustion and dysfunction of T cells, which limit its
 clinical use. Tumor-draining lymph node-derived lymphocytes (LNLs) that have abundant
 tumor-specific T cells, rather than exhausted T cells, are easier to produce. It is not yet
 known whether LNL treatment is safe and effective in patients with advanced HER2-negative
 breast cancer.
 
 PURPOSE: This phase I trial is mainly to study the safety of autologous LNL in patients with
 advanced HER2-negative breast cancer.
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT06121557
Non-Device Trial