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Post-marketing Surveillance Protocol Number; CABL001A1401

Special drug use-results surveillance of Scemblix Tablets(resistant or intolerant chronic myeloid leukemia)

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT2031220191
Enrollment
440
Registered
2022-07-07
Start date
2022-07-01
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

Chronic myeloid leukemia resistant or intolerant to pretreatment drugs

Interventions

None listed

Sponsors

Toshiya Sugimoto
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All patients treated with asciminib

Exclusion criteria

Exclusion criteria: none

Design outcomes

Primary

MeasureTime frame
To assess the safety profile of the safety specifications (myelosuppression, infections, QT interval prolongation, pancreatitis, vascular occlusive events, photosensitivity)

Contacts

Public ContactNovartis Direct

Novartis Pharma. K.K.

sm.pms@novartis.com+81-120003293

Outcome results

None listed

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