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NCT03375567

Global Response Assessment by Advanced Imaging and Myeloma Lesion Biopsies During Induction Therapy of Multiple Myeloma With Carfilzomib Lenalidomide Dexamethasone

Completed NA Last updated 24 February 2022
What this trial tests

NA trial testing Guided Lesion Biopsies in Multiple Myeloma in 28 participants. Completed in 14 January 2022.

Timeline
4 June 2018
Primary endpoint
14 January 2022
14 January 2022

Quick facts

Lead sponsorYale University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment28
Start date4 June 2018
Primary completion14 January 2022
Estimated completion14 January 2022
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Yale University

Who can join

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

Sponsor's own description

The primary objective of this study is to compare the detection rate of residual/refractory disease based on standard bone marrow biopsy versus guided myeloma lesion biopsy after induction therapy with carfilzomib, lenalidomide and dexamethasone regimen.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Targeting the proteasome in cancer therapy: development and future opportunities in natural products.
    Zhao X, Liu S, Zeng X, Liao Y, et al · · 2026 · PMID 42158938 · DOI 10.3389/fphar.2026.1806787

Verify or expand the search:

Other recruiting trials for Multiple Myeloma

Currently open trials in the same condition.

Other Yale University 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/NCT03375567.

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