Efficacy and Safety of Obinutuzumab in Combination With Lenalidomide in Patients With Relapsed and Refractory Follicular Lymphoma (R/R FL): A Prospective Observational Study

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

This study is planned to prospectively observe and verify the efficacy and safety of induction therapy with obinutuzumab in combination with lenalidomide followed by maintenance therapy with obinutuzumab and lenalidomide in patients with R/R FL in a real-world setting in a Chinese population.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
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⁃ Patients must meet the following criteria for study entry::

• Signed Informed Consent Form

• Age ≥ 18 years at enrollment

• At least one prior line of systemic (Stage III-IV) follicular lymphoma therapy

• Relapsed or refractory to front-line anti-lymphoma therapy; refractory is defined as: tumor shrinkage of less than 50% or disease progression after 4 cycles of standard regimen chemotherapy; response to standard regimen chemotherapy, relapse within 24 months; 2 or more relapses, meeting one of the above criteria as refractory lymphoma.

• Conditional treatment with obinutuzumab in combination with lenalidomide

Locations
Other Locations
China
Institute of Hematology and Blood Diseases Hospital ,Chinese Academy of Medical Sciences
RECRUITING
Tianjin
Contact Information
Primary
shuhua Yi, Dr
yishuhua@ihcams.ac.cn
86-22-23909106
Backup
Lugui Qiu, Dr
qiulg@ihcams.ac.cn
86-22-23909172
Time Frame
Start Date: 2022-11-01
Estimated Completion Date: 2028-05-31
Participants
Target number of participants: 50
Sponsors
Leads: Institute of Hematology & Blood Diseases Hospital, China

This content was sourced from clinicaltrials.gov

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