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COMPLETED
NCT05105841
PHASE2

Study to Assess Change in Disease Activity and Adverse Events of Oral Venetoclax in Combination With Intravenous (IV) Obinutuzumab or Oral Ibrutinib in Adult Participants With Untreated Chronic Lymphocytic Leukemia (CLL)/Small Lymphocytic Lymphoma (SLL)

Sponsor: AbbVie

View on ClinicalTrials.gov

Summary

Chronic lymphocytic leukemia (CLL) is the most common leukemia in Western countries, representing approximately 30% of all adult leukemias. There is a large difference in proportion of malignant lymphoma between the United States (US) and Japan was seen in CLL/small lymphocytic lymphoma (SLL) (Japan, 3.2%; US, 24.1%). The purpose of this study is to assess how well venetoclax works in combination with obinutuzumab (V+G, Cohort 1) or with ibrutinib (V+I, Cohort 2) in Japanese participants with previously untreated CLL/Small Lymphocytic Lymphoma (SLL). Adverse events and change in disease activity will be assessed. Venetoclax is an approved drug for the treatment of CLL and SLL. Study doctors put the participants in 1 of 2 groups, called treatment arms, based on variable alternating assignment. Approximately 20 adult participants with previously untreated CLL/SLL will be enrolled in the study in approximately 20 sites in Japan. Participants in group 1 will receive oral venetoclax + intravenous (IV) obinutuzumab (V+G) in 28-day cycles for a total of 12 cycles, and participants in group 2 will receive oral venetoclax + oral ibrutinib (V+I) in 28-day cycles for a total of 15 cycles. 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.

Official title: A Phase 2 Study of the Safety and Efficacy of Venetoclax in Combination With Obinutuzumab or Ibrutinib in Japanese Subjects With Previously Untreated Chronic Lymphocytic Leukemia (CLL)/Small Lymphocytic Lymphoma (SLL)

Key Details

Gender

All

Age Range

20 Years - Any

Study Type

INTERVENTIONAL

Enrollment

20

Start Date

2021-11-08

Completion Date

2025-10-09

Last Updated

2026-10-21

Healthy Volunteers

No

Interventions

DRUG

Venetoclax

Oral Tablet

DRUG

Ibrutinib

Oral Capsule

DRUG

Obinutuzumab

Intravenous (IV) Infusion

Locations (20)

NHO Nagoya Medical Center /ID# 233523

Nagoya, Aichi-ken, Japan

Aichi Cancer Center Hospital /ID# 238797

Nagoya, Aichi-ken, Japan

Japanese Red Cross Aichi Medical Center Nagoya Daini Hospital /ID# 233524

Nagoya, Aichi-ken, Japan

Chiba Cancer Center /ID# 238839

Chiba, Chiba, Japan

National Hospital Organization Shikoku Cancer Center /ID# 234059

Matsuyama, Ehime, Japan

Kyushu University Hospital /ID# 238437

Fukuoka, Fukuoka, Japan

Hokkaido University Hospital /ID# 238377

Sapporo, Hokkaido, Japan

Hyogo Prefectural Amagasaki General Medical Center /ID# 234082

Amagasaki-shi, Hyōgo, Japan

Tokai University Hospital /ID# 238970

Isehara, Kanagawa, Japan

University Hospital Kyoto Prefectural University of Medicine /ID# 239883

Kyoto, Kyoto, Japan

Tohoku University Hospital /ID# 238433

Sendai, Miyagi, Japan

Niigata University Medical & Dental Hospital /ID# 238324

Niigata, Niigata, Japan

Okayama University Hospital /ID# 238467

Okayama, Okayama-ken, Japan

Kindai University Hospital /ID# 234001

Sakai-shi, Osaka, Japan

Osaka University Hospital /ID# 234037

Suita-shi, Osaka, Japan

Shimane University Hospital /ID# 234076

Izumo-shi, Shimane, Japan

Jichi Medical University Hospital /ID# 238434

Shimotsuke-shi, Tochigi, Japan

National Cancer Center Hospital /ID# 232449

Chuo-ku, Tokyo, Japan

The Cancer Institute Hospital Of JFCR /ID# 232450

Koto-ku, Tokyo, Japan

Yamagata University Hospital /ID# 234032

Yamagata, Yamagata, Japan