Skip to content

Tibsovo Tablets 250 mg General Drug Use-Results Survey (IDH1-mutated acute myeloid leukaemia)

Tibsovo Tablets 250 mg General Drug Use-Results Survey (IDH1-mutated acute myeloid leukaemia) - Tibsovo Tablets General Drug Use-Results Survey (IDH1-mutated acute myeloid leukaemia)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000058014
Enrollment
268
Registered
2025-06-02
Start date
2025-06-02
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

IDH1-mutated acute myeloid leukaemia

Interventions

None listed

Sponsors

NIHON SERVIER CO., LTD.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with IDH1-mutated acute myeloid leukaemia who received this drug for the first time during the study period and agreed to participate in this study.

Exclusion criteria

Exclusion criteria: No given consent to participation in the survey.

Design outcomes

Primary

MeasureTime frame
Incidence of the side effect of Guillain-Barre syndrome

Secondary

MeasureTime frame
Efficacy and safety in patients with IDH1-mutated AML

Countries

Japan

Contacts

Public ContactDaisuke Tanaka

NIHON SERVIER CO., LTD. DRUG SAFETY & REAL WORLD EVIDENCE

daisuke.tanaka@servier.com07075969589

Outcome results

None listed

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