Long-term Non-interventional Observational Study Following Treatment With Fate Therapeutics FT500 Cellular Immunotherapy

  • STATUS
    Recruiting
  • End date
    Dec 23, 2034
  • participants needed
    76
  • sponsor
    Fate Therapeutics
Updated on 23 January 2021

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 Subjects will automatically enroll into study FT-003 once they have withdrawn or complete the parent interventional study.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.

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.

Details
Condition Pancreatic Cancer, Non-Small Cell Lung Cancer, Cervical Cancer, Adenocarcinoma, Colorectal Cancer, Disorders of cervix NOS, Microsatellite Instability, Malignant neoplasm of kidney, Rectal disorder, Neuroendocrine carcinoma, Uterine Cancer, Lymphoma, Carcinoma, melanoma, Squamous cell carcinoma, Transitional cell carcinoma, Renal Cell Carcinoma, skin cancer, HEPATIC NEOPLASM, Lymphoproliferative Disorder, Lymphoma, Small Cell Lung Cancer, HEPATOCELLULAR CARCINOMA, Gastropathy, Gastric Cancer, Merkel cell carcinoma, head and neck cancer, Stomach Discomfort, Metastatic Melanoma, Vulvar Dysplasia and Carcinoma, Non-Hodgkin's Lymphoma, Colon Cancer Screening, Rectal Disorders, Colon cancer; rectal cancer, Advanced Solid Tumor, HER2 Positive Breast Cancer, Gastric Carcinoma, Advanced Malignancies, Islet Ce417ll Cancer, EGFR Positive Solid Tumor, Advanced Malignant Solid Tumor, Kidney Cancer, Malignant Melanoma, Liver Cancer, Malignant Adenoma, Stomach Cancer, Renal Cell Cancer, Renal Cancer, Lymphoproliferative disorders, Urothelial Carcinoma, cervical carcinoma, clear cell renal cell carcinoma, colorectal neoplasm, gastric cancers, her2/neu-positive breast cancer, her2-positive breast cancer, colorectal cancers, lymphomas, nsclc, cancer of the head and neck, cervical cancer, uterine, cancer of the pancreas, carcinoma of the cervix uteri, carcinoma of the cervix, cervix cancer, cancer of the cervix, carcinoma of cervix, epidermoid carcinoma, squamous cell cancer, pancreatic cancers, cancer, pancreatic, liver cell carcinoma, cancer, colorectal, colorectal tumor, tumors, colorectal, sclc, small cell carcinoma, small cell carcinoma of the lung
Treatment Allogeneic natural killer (NK) cell
Clinical Study IdentifierNCT04106167
SponsorFate Therapeutics
Last Modified on23 January 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Is your age greater than or equal to 18 yrs?
Gender: Male or Female
Do you have any of these conditions: Advanced Malignancies or Lymphoma or carcinoma of cervix or Advanced Malignant Solid Tumor or Colon cancer; rectal cancer or squamous cell cancer or G...?
Subjects who received an allogeneic, iPSC-derived NK cell in a Fate Therapeutics interventional study
Subjects who have provided Informed consent prior to their study participation

Exclusion Criteria

Not Applicable
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