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A Phase 2 Study of Venetoclax Monotherapy in Japanese Subjects With Relapsed or Refractory Waldenström Macroglobulinemia/Lymphoplasmacytic Lymphoma

Status: Recruiting
Location: See all (7) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Lymphoplasmacytic Lymphoma (LPL) is a rare type of low-grade B-cell lymphoma. The purpose of this study is to assess the change in disease activity of adult participants with relapsed or refractory Waldenström macroglobulinemia(WM)/LPL receiving venetoclax. Venetoclax is being investigated in the treatment of WM/LPL. Participants will receive oral venetoclax at doses ramping up to the target dose, as part of treatment. Approximately 14 adult participants with WM/LPL will be enrolled in the study at approximately 20 sites in Japan. Participants will receive oral venetoclax at doses ramping up to the target dose. The total study duration is approximately 28 months. There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at a hospital or clinic. The effect of the treatment will be checked by medical assessments, blood tests, and checking for side effects.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Documented diagnosis of Waldenström macroglobulinemia(WM) /lymphoplasmacytic lymphoma (LPL) according to the 5th edition of the World Health Organization (WHO) classification and/or documented clinicopathological diagnosis of WM in accordance with the consensus panel of the second International Workshop on WM (IWWM).

• At least one prior standard therapy for WM/LPL.

• Measurable disease, defined as follows:

‣ WM type LPL population: Immunoglobulin M (IgM) \>= 500 mg/dL per central laboratory (approximately 14 participants)

⁃ Non-IgM type LPL population or IgM \< 500 mg/dL: A measurable node having a longest diameter (LDi) greater than 1.5 cm, or a measurable extranodal disease having a LDi greater than 1.0 cm, according to contrast-enhanced computed tomography (CT) scan. (up to 2 participants)

• Requires systemic anti-cancer treatment for WM/LPL, according to the investigator.

• Eastern Cooperative Oncology Group Performance Status \< = 2

• Adequate organ and bone marrow function

Locations
Other Locations
Japan
The University of Tokyo Hospital /ID# 279174
RECRUITING
Bunkyo-ku
National Cancer Center Hospital /ID# 279076
RECRUITING
Chuo-ku
NHO Mito Medical Center /ID# 279175
RECRUITING
Higashiibaraki-gun
Gunma University Hospital /ID# 277576
RECRUITING
Maebashi
Nagoya City University Hospital /ID# 277580
RECRUITING
Nagoya
National Hospital Organization Disaster Medical Center /ID# 277741
RECRUITING
Tachikawa
University of Fukui Hospital /ID# 279173
RECRUITING
Yoshida-gun
Contact Information
Primary
ABBVIE CALL CENTER
abbvieclinicaltrials@abbvie.com
844-663-3742
Time Frame
Start Date: 2026-03-17
Estimated Completion Date: 2028-07
Participants
Target number of participants: 14
Treatments
Experimental: Venetoclax Monotherapy
Participants will receive venetoclax at doses ramping up to the target dose, as part of the approximately 28 month study duration.
Sponsors
Leads: AbbVie

This content was sourced from clinicaltrials.gov