A Phase 2 interventional study of IBI376 in Indolent Non-hodgkin Lymphoma, sponsored by Innovent Biologics (Suzhou) Co. Ltd.. Completed at 1 site in China. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-06-05.
Sponsored by Innovent Biologics (Suzhou) Co. Ltd. · Phase 2, Interventional, and Treatment
A Phase 2, Multicenter, Open-Label Study of IBI376, a PI3Kδ Inhibitor, in Patients with Relapsed or Refractory Follicular Lymphoma/Marginal Zone Lymphoma
Patients will be recruited for 2 cohorts. Cohort A will recruit 58 RRFL subjects, and Cohort B will recruit 62 RRMZL subjects.
5,578 studies on the registry are indexed under Lymphoma; 825 are open to participants now.
This study's enrollment of 81 is above the median of 40 across 4,508 interventional studies indexed under Lymphoma.
Browse Lymphoma studies →Innovent Biologics (Suzhou) Co. Ltd. is the lead sponsor of 192 studies on the registry; 44 are open to participants now.
Of its 5 completed or terminated interventional studies of FDA-regulated products, 1 (20%) have results posted.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
1 . Known histological transformation from indolent NHL to diffuse large B-cell lymphoma.
IBI376 will be administered orally at a dose of 20 mg once daily for 8 weeks followed by 2.5 mg once daily.
Drug: IBI376
IBI376 20 mg po. once daily for 8 weeks ,followed by 2.5mg once daily
Also known as: Parsaclisib
Objective Response Rate (ORR)
To assess the efficacy of IBI376 in terms of objective response rate (ORR) in subjects with relapsed or refractory follicular lymphoma (FL)/Marginal lymphoma(MZL). Subjects will be evaluated for ORR by an IRC (Lugano criteria)
Time frame: 2 years
Complete Response Rate (CRR)
To assess complete response rate (CRR)
Time frame: 2 years
Duration of Response (DOR)
To assess the duration of response (DOR)
Time frame: 2 years
Progression-free Survival (PFS)
To assess progression-free survival (PFS)
Time frame: 2 years
Overall Survival (OS)
To assess overall survival (OS)
Time frame: 2 years
Best percentage change in target lesion size
To assess best percentage change in target lesion size
Time frame: 2 years
Safety and tolerability of IBI376 measured by adverse events (AEs)
Defined as any AE either reported for the first time or worsening of a pre-existing event after first dose of study treatment.
Time frame: Baseline through 30-35 days after end of treatment, up to approximately 12 months per subject
This study is completed, as verified in Jun 2024. You cannot join it, but the record below documents what was studied.
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Innovent Biologics (Suzhou) Co. Ltd.