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Clinical Trial Summary

Subjects who previously took part in the FT500-101 study and received allogeneic NK cell immunotherapy will take part in this long term follow-up study. Subjects will automatically enroll into study FT-003 once they have withdrawn or complete the parent interventional study. The purpose of this study is to provide long-term safety and survival data for subjects who have participated in the parent study. No additional study drug will be given, but subjects can receive other therapies for their cancer while they are being followed for long term safety in this study.


Clinical Trial Description

This is a multicenter, non-interventional, observation study designed to provide long-term safety and efficacy data on subjects who have participated in a prior Fate Therapeutics interventional study of FT500 cellular immunotherapy. Subjects will be contacted every six months (± one month), beginning six months after subject completion or withdrawal from the FT500-101 study. ;


Study Design


Related Conditions & MeSH terms

  • Advanced Solid Tumor
  • Carcinoma
  • Carcinoma, Merkel Cell
  • Carcinoma, Renal Cell
  • Cervical Cancer
  • Colorectal Cancer
  • EGFR Positive Solid Tumor
  • Gastric Cancer
  • Head and Neck Cancer
  • Hepatocellular Carcinoma
  • HER2-positive Breast Cancer
  • Lymphoma
  • Melanoma
  • Merkel Cell Carcinoma
  • Microsatellite Instability
  • NSCLC
  • Pancreas Cancer
  • Pancreatic Neoplasms
  • Renal Cell Carcinoma
  • Small Cell Lung Carcinoma
  • Small-cell Lung Cancer
  • Squamous Cell Carcinoma
  • Urothelial Carcinoma

NCT number NCT04106167
Study type Observational
Source Fate Therapeutics
Contact
Status Terminated
Phase
Start date June 11, 2019
Completion date August 11, 2023

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