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Clinical Trial Summary

hMe-Seal is a low-input whole-genome cell-free 5hmC sequencing method based on selective chemical labeling. It uses β-glucosyltransferase (βGT) to selectively label 5hmC with a biotin via an azide-modified glucose for pull-down of 5hmC-containing DNA fragments for sequencing. After selectively constructing 5hmC library, highthroughput-sequencing will be performed on an Illumina Nextseq-500 instrument. By ways of Rawdata processing, differential loci between Osteosarcoma group and control group will be detected to indentify specific epigenetic biomarkers of Osteosarcoma. From our previous trials, we identify geno sequencing related to beta-catenin pathways might have some relationship with osteosaroma primary or secondary drug resistance. Thus in this trial we try to further explore the drug resistance mechanism for advaced osteosarcoma second resistance to the combination therapy of Famitinib and Camrelizumab.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Biomarkers for Efficacy and Toxicity
  • Drug Resistance to Famitinib and Camrelizumab
  • Osteosarcoma

NCT number NCT03919539
Study type Observational [Patient Registry]
Source Peking University People's Hospital
Contact Lu Xie, M.D.
Phone +8613401044719
Email xie.lu@hotmail.com
Status Recruiting
Phase
Start date December 1, 2019
Completion date December 31, 2021