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Not Yet RecruitingNCT06981988

A Study of Linperlisib (YY-20394) in Combination With Rituximab in Patients With Relapsed/Refractory Indolent NHL

A Study to Explore the Dosage and Efficacy of Linperlisib in Combination With Rituximab and to Validate the Efficacy of Linperlisib in Patients With Relapsed/Refractory Indolent NHL

Status
Not Yet Recruiting
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
80 (estimated)
Sponsor
Jiangsu HengRui Medicine Co., Ltd. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The study is being conducted to evaluate the reasonable dosage, efficacy and safety of Linperlisib in combination with rituximab in subjects with relapsed/refractory (R/R) indolent non-hodgkin lymphoma(NHL) in adults.

Conditions

Interventions

TypeNameDescription
DRUGLinperlisib ; RituximabLinperlisib ; Rituximab

Timeline

Start date
2025-06-01
Primary completion
2025-08-01
Completion
2027-02-01
First posted
2025-05-21
Last updated
2025-05-21

Source: ClinicalTrials.gov record NCT06981988. Inclusion in this directory is not an endorsement.

A Study of Linperlisib (YY-20394) in Combination With Rituximab in Patients With Relapsed/Refractory Indolent NHL (NCT06981988) · Clinical Trials Directory