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GAZYVA, Special Drug Use Surveillance -Patients with CD20-positive follicular lymphoma-

GAZYVA, Special Drug Use Surveillance -Patients with CD20-positive follicular lymphoma- - GAZYVA, Special Drug Use Surveillance -Patients with CD20-positive follicular lymphoma-

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000033864
Enrollment
1000
Registered
2018-10-20
Start date
2018-10-22
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

CD20-positive follicular lymphoma

Interventions

None listed

Sponsors

Chugai Pharmaceutical Co. Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with CD20-positive follicular lymphoma planning to use obinutuzumab during the enrollment period.

Exclusion criteria

Exclusion criteria: not applicable

Design outcomes

Primary

MeasureTime frame
The incidence proportion of Grade >=3 infection

Countries

Japan

Contacts

Public ContactAyako Murayama

Chugai Pharmaceutical Co. Ltd. Safety Science Dept.

murayamaayk@chugai-pharm.co.jp03-3281-6611

Outcome results

None listed

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