Observational Study in Japanese Patients With Peripheral T-Cell Lymphoma Who Received Second-Line Therapy

NCT06422247 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 307

Last updated 2025-06-04

No results posted yet for this study

Summary

The purpose of this study is to describe the therapeutic practices and the prognosis of patients with relapsed or refractory peripheral T-cell lymphoma in Japan

Conditions

  • Peripheral T-cell Lymphoma

Interventions

DRUG

Systemic therapy

Approved peripheral T-cell lymphoma systemic treatments prescribed by the treating physician

Sponsors & Collaborators

Principal Investigators

  • Bristol-Myers Squibb · Bristol-Myers Squibb

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-04-05
Primary Completion
2025-02-05
Completion
2025-02-05
FDA Drug
Yes

Countries

  • Japan

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Entities

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 NCT06422247 on ClinicalTrials.gov