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Study to evaluate the addition of an experimental drug, CC-90010, to the usual treatment of brain cancer after surgery

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-511171-15-00
Acronym
CC-90010-GBM-002
Enrollment
216
Registered
2024-04-03
Start date
2020-07-06
Completion date
2024-04-18
Last updated
2024-07-04

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

Conditions

Subjects with newly diagnosed WHO Grade IV glioblastoma (ndGBM) who have undergone complete or partial tumor resection

Interventions

None listed

Sponsors

Celgene Corp., Celgene Corp.
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Countries

Denmark, Italy, Netherlands, Norway, Spain, Sweden

Outcome results

None listed

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