An Early Access Programme for Moxetumomab Pasudotox in Relapsed/Refractory Hairy Cell Leukemia

NCT03501615 · Status: APPROVED_FOR_MARKETING · Type: EXPANDED_ACCESS

Last updated 2020-06-29

No results posted yet for this study

Summary

Early Access Programme to provide treatment access to moxetumomab pasudotox for eligible patients with relapsed/refractory hairy cell leukemia

Conditions

  • Relapsed/Refractory Hairy Cell Leukemia

Interventions

DRUG

Moxetumomab Pasudotox

A recombinant conjugated immunotoxin composed of a disulfide-stabilized anti-CD22 Ig Fv genetically fused to a truncated form of Pseudomonas exotoxin, PE38

Sponsors & Collaborators

Principal Investigators

  • Nai Shun (Nancy) Yao, MD · MedImmune LLC

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03501615 on ClinicalTrials.gov