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MinorTrial completedPrimary and study completion dates changed from estimate of Aug 31, 2026 to Sep 1, 2026 · Eligibility criteria expanded, about 10 words · Secondary endpoints: details revised at 3 of 12 entriesShow 3 more changesShow less
Primary and study completion dates changed from estimate of Aug 31, 2026 to Sep 1, 2026
Eligibility criteria expanded, about 10 words
Secondary endpoints: details revised at 3 of 12 entries
MinorPrimary and study completion pushed from Jun 2026 to Aug 31, 2026v14
MinorPrimary and study completion dates: Apr 2026 to Jun 2026v13
MinorRe-verified, no change to tracked fieldsv12
Show 10 earlier versionsHide 10 earlier versions
MinorStudy sites: 10 to 11v11
MinorRe-verified, no change to tracked fieldsv10
NotablePrimary and study completion dates: May 2024 to Apr 2026v9
MinorTrial status: Recruiting to Active, Not RecruitingEnrollment target: estimated 70 to confirmed 64 · Site details revised at 10 of 10 sitesv8Show 2 more changesShow less
Enrollment target: estimated 70 to confirmed 64
Site details revised at 10 of 10 sites
MinorStudy sites: 11 to 10v7
MinorRe-verified, no change to tracked fieldsv6
MinorStudy sites: 1 to 11v5
MinorRe-verified, no change to tracked fieldsv4
NotableEnrollment target: 40 to 70v3
NotableTrial status: Not Yet Recruiting to RecruitingStart date changed from estimate of Jun 2021 to Jul 5, 2021 · Site details revisedv2Show 2 more changesShow less
Start date changed from estimate of Jun 2021 to Jul 5, 2021
Site details revised
MinorStudy First Submitted
Stopped: an ongoing trial was terminated, suspended or withdrawn.
Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The purpose of this study is to evaluate the safety and tolerability of BGB-11417 monotherapy, define the maximum tolerated dose (MTD) or maximum administered dose and the recommended Phase 2 dose (RP2D) of BGB-11417 monotherapy for the selected B-cell malignancy dose finding cohorts, and evaluate the safety and tolerability of the ramp-up dosing schedule in the evaluated disease types.