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Integrated analysis of the past mogamulizumab clinical trials

Integrated analysis of the past mogamulizumab clinical trials for patients with ATL, PTCL and CTCL - Integrated analysis of the past mogamulizumab clinical trials for patients with ATL, PTCL and CTCL

Status
Active, not recruiting
Phases
Unknown
Study type
Unknown
Source
JPRN
Registry ID
JPRN-UMIN000053792
Enrollment
625
Registered
2024-03-31
Start date
2024-04-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

CCR4-positive Adult T-cell leukemia/lymphoma CCR4-positive Peripheral T-cell lymphoma Cutaneous T-cell lymphoma

Interventions

None listed

Sponsors

Kyowa Kirin Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients whose data was recorded participating the following clinical trials: Phase 2 trial investigating mogamulizumab efficacy and safety for relapsed ATL patients Phase 2 trial comparing mogamulizumab efficacy and safety with investigator's choice for relapsed/refractory ATL patients Phase 2 clinical trial comparing efficacy and safety of mLSG15+mogamulizumab combination therapy with mLSG15 alone for untreated ATL patients Phase 2 trial investigating mogamulizumab efficacy and safety for relapsed PTCL patients Phase 2 trial investigating mogamulizumab efficacy and safety for relapsed/refractory PTCL patients Phase 1/2 trial investigating mogamulizumab efficacy and safety for relapsed/refractory CTCL patients Phase 3 trial comparing mogamulizumab efficacy and safety with vorinostat for relapsed/refractory CTCL patients

Exclusion criteria

Exclusion criteria: Patients participated the below trials but did not take mogamulizumab administration. Phase 2 trial comparing mogamulizumab efficacy and safety with investigator's choice for relapsed/refractory ATL patients Phase 3 trial comparing mogamulizumab efficacy and safety with vorinostat for relapsed/refractory CTCL patients

Design outcomes

Primary

MeasureTime frame
Blood parameter changes

Secondary

MeasureTime frame
Plasma concentration changes of mogamulizumab Generalized models of blood parameters

Countries

Japan,North America,South America,Europe

Contacts

Public ContactYukihiro Nishio

Kyowa Kirin Co., Ltd. Medical Affairs

hqmarinkensuit.sh@kyowakirin.com03-5205-7200

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026