RecruitingPhase 2NCT07387471
Study to Assess Change in Disease Activity of Oral Venetoclax in Adult Participants With Recurring Relapsed or Refractory (R/R) Waldenström Macroglobulinemia (WM)/Lymphoplasmacytic Lymphoma (LPL)
Studying Waldenström macroglobulinemia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- AbbVie
- Principal Investigator
- ABBVIE INC.AbbVie
- Intervention
- Venetoclax(drug)
- Enrollment
- 14 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2026 – 2028
Study locations (3)
- NHO Mito Medical Center /ID# 279175, Higashiibaraki-gun, Ibaraki, Japan
- National Cancer Center Hospital /ID# 279076, Chuo-Ku, Tokyo, Japan
- National Hospital Organization Disaster Medical Center /ID# 277741, Tachikawa, Tokyo, Japan
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT07387471 on ClinicalTrials.govOther trials for Waldenström macroglobulinemia
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