OMIX

A Clinical Study of GC012F Injection in High-risk, Transplant Eligible Patients with Newly Diagnosed Multiple Myeloma

OMIX005753

1Summary
Title A Clinical Study of GC012F Injection in High-risk, Transplant Eligible Patients with Newly Diagnosed Multiple Myeloma
Description This study was a single-arm, single-center, open-label clinical study to evaluate the safety and efficacy of GC012F in high-risk, transplantation-eligible NDMM patients. The study was planned to include 20 evaluable subjects. A total of two cycles of induction therapy (bortezomib-based three-drug regimen, with details determined by the investigator on the basis of the patient) were selectively administered before or after collection in eligible subjects. Participants will then receive a single GC012F infusion, with response assessments at 1 month, 3 months, and every 3 months thereafter for 2 years until the end of the trial (each response assessment will require MRD testing).
Organism Homo sapiens
Data Type Genetic Biomarkers
Data Accessibility Controlled-access
BioProject PRJCA023219
Release Date 2024-01-27
Submitter mingyue xiang (mingyue.xiang@gracellbio.com)
Organization Gracell Biotechnologies Inc
Submission Date 2024-01-26
2Files & Download

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File ID File Title Number/Samples File Type File Size File Suffix Download Times Download
OMIX005753-01 NDMM IIT 1 Genetic Biomarkers 57.9 KB xlsx 0 Controlled

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