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NCT04125290: PROXY

US Post-Marketing Safety Study of Moxetumomab Pasudotox-tdfk (LUMOXITI)

Terminated Last updated 18 July 2025
What this trial tests

trial in Hairy Cell Leukemia in 2 participants. Terminated before completion.

Timeline
9 December 2019
Primary endpoint
21 June 2021
21 June 2021

Quick facts

Lead sponsorAstraZeneca
StatusTerminated
Study typeOBSERVATIONAL
Enrollment2
Start date9 December 2019
Primary completion21 June 2021
Estimated completion21 June 2021
Sites2 locations across United States

Conditions studied

Sponsor

AstraZeneca — full company profile →

Who can join

Eligibility, any sex, with Hairy Cell Leukemia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is being conducted to satisfy a post-marketing requirement (PMR) to provide evidence characterizing 1) the safety of moxetumomab pasudotox-tdfk in patients who are 65 years of age and older and/or 2) the safety of moxetumomab pasudotox-tdfk in patients who have moderate renal impairment defined as an estimated GFR of 30-59 ml/min

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Phage Display Derived Monoclonal Antibodies: From Bench to Bedside.
    Alfaleh MA, Alsaab HO, Mahmoud AB, Alkayyal AA, et al · · 2020 · cited 194× · PMID 32983137 · DOI 10.3389/fimmu.2020.01986
  2. The protective role of the microenvironment in hairy cell leukemia treatment: Facts and perspectives.
    Gargiulo E, Giordano M, Niemann CU, Moussay E, et al · · 2023 · cited 2× · PMID 36968995 · DOI 10.3389/fonc.2023.1122699

Verify or expand the search:

Other recruiting trials for Hairy Cell Leukemia

Currently open trials in the same condition.

Other AstraZeneca 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/NCT04125290.

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