Azercabtagene zapreleucel (azer-cel)
DrugIV infusion
NCT Number: NCT06680037
The main objective of the study is to determine the recommended phase 2 dose (RP2D) of Azercabtagene zapreleucel (azer-cel).
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 1
TG Therapeutics Investigational Trial Site, La Jolla, California, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
PMS and RMS inclusion criteria:
NMOSD inclusion criteria:
MG Inclusion criteria:
CIDP Inclusion criteria
General Exclusion Criteria:
Note: Other protocol-specified Inclusion/Exclusion criteria may apply.
IV infusion
Time frame: From Day 0 to Day 28
DLT will be determined using the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 5.0.
Time frame: Up to Day 720
Time frame: Baseline, up to Day 720
Time frame: Up to Day 720
Time frame: Up to Day 720
Time frame: Up to Day 720
Time frame: Up to Day 720
Time frame: Baseline, up to Day 720
Time frame: Baseline, up to Day 720
Time frame: Baseline, up to Day 720
Time frame: Baseline, up to Day 720
Time frame: Baseline, up to Day 720
Time frame: Baseline, up to Day 720
Time frame: Baseline, up to Day 720
Time frame: Baseline, up to Day 720
Contact information is provided by the study sponsor or research team.
TG Therapeutics, Inc.
Industry
A Phase 1, Open-label Study to Evaluate the Safety and Clinical Activity of Azercabtagene Zapreleucel in Participants With B-cell Mediated Autoimmune Disorders
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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