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NCT06369935

A Real World Study of Equecabtagene Autoleucel in Subjects With Relapsed and Refractory Multiple Myeloma.

Not yet recruiting Last updated 17 April 2024
What this trial tests

trial testing Equecabtagene Autoleucel in Relapsed/Refractory Multiple Myeloma in 260 participants. Not yet recruiting.

Timeline
20 June 2024
Primary endpoint
20 August 2026
20 August 2027

Quick facts

Lead sponsorPeking University People's Hospital
StatusNot yet recruiting
Study typeOBSERVATIONAL
Enrollment260
Start date20 June 2024
Primary completion20 August 2026
Estimated completion20 August 2027
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Peking University People's Hospital

Who can join

18 and older, any sex, with Relapsed/Refractory Multiple Myeloma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is a multicenter, observational, single-arm real world study. The purpose of this study is to describe demographic and disease characteristics, treatment patterns, and clinical outcomes in the real-world setting among participants in China with relapsed/refractory multiple myeloma (RRMM) who have been treated with Equecabtagene Autoleucel. This study will use both prospective and retrospective data

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Relapsed/Refractory Multiple Myeloma

Currently open trials in the same condition.

Other Peking University People's Hospital 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/NCT06369935.

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