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Fixed-duration therapy with ibrutinib and obinutuzumab (GA-101) in treatment-naïve patients with CLL

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-514824-18-00
Enrollment
53
Registered
2024-08-05
Start date
2021-09-16
Completion date
Unknown
Last updated
2024-08-05

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

Conditions

chronic lymphocytic leukemia/small lymphocytic lymphoma

Brief summary

Percentage of patients with MRD <10-4 in BM at +30 follow-up days after completion of therapy

Interventions

DRUGOBINUTUZUMAB
DRUGIBRUTINIB

Sponsors

Ospedale San Raffaele S.r.l.
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Percentage of patients with MRD <10-4 in BM at +30 follow-up days after completion of therapy

Countries

Italy

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026