Last reviewed · How we verify

NCT07365059

Safety and Efficacy of GPRC5D CAR-T Cell Therapy in Relapsed/Refractory Plasma Cell Disorders

Not yet recruiting EARLY_PHASE1 Last updated 26 January 2026
What this trial tests

EARLY_PHASE1 trial testing GPRC5D CAR-T cell intravenous infusion in Plasma Cell Dyscrasias in 18 participants. Not yet recruiting.

Timeline
25 January 2026
Primary endpoint
1 January 2029
1 March 2029

Quick facts

Lead sponsorQi deng
PhaseEARLY_PHASE1
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment18
Start date25 January 2026
Primary completion1 January 2029
Estimated completion1 March 2029

Drugs / interventions tested

Conditions studied

Sponsor

Qi deng — full company profile →

Who can join

Adults 14 to 75, any sex, with Plasma Cell Dyscrasias. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is an open-label, single-arm, dose-escalation and expansion, prospective clinical trial. It enrolls patients with relapsed/refractory plasma cell disorders, administers GPRC5D CAR-T cell therapy, follows up to observe adverse reactions after medication, collects relevant data on treatment efficacy, evaluates the safety and efficacy of CAR-T cells, and simultaneously investigates the cellular kinetic characteristics of CAR-T cells.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other recruiting trials for Plasma Cell Dyscrasias

Currently open trials in the same condition.

Other Qi deng trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07365059.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing