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General drug use-results survey of Hiyasta tablets (PTCL)

General drug use-results survey of Hiyasta tablets for Relapsed or Refractory Peripheral T-cell Lymphoma (PTCL) All-Case Survey

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT2031210606
Enrollment
170
Registered
2022-02-10
Start date
2022-02-21
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

Relapsed or Refractory Peripheral T-cell Lymphoma (PTCL)

Interventions

None listed

Sponsors

Post Marketing Surveillance Post Marketing Surveillance Dept.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All patients with relapsed or refractory PTCL to whom Hiyasta tablets is administered. Patients in whom recurrent or refractory peripheral T-cell lymphoma (PTCL) was histologically diagnosed.

Exclusion criteria

Exclusion criteria: none

Design outcomes

Primary

MeasureTime frame
To assess the occurrence of " myelosuppression", " interstitial lung disease", "infectious disease", and "arrhythmia (including QT interval prolongation)" under actual use conditions in patients with relapsed or refractory PTCL treated with tucidinostat.

Contacts

Public ContactPost Marketing Surveillance Dept. Post Marketing Surveillance

Meiji Seika Pharma CO., Ltd.

hiyasta_pms@meiji.com+81-3-3273-3395

Outcome results

None listed

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