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A Phase II Study of YHI-1702

A Phase II Study of YHI-1702 (duvelisib) in Patients with Relapsed or Refractory Follicular Lymphoma

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2031210529
Enrollment
36
Registered
2021-12-28
Start date
2022-05-26
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Follicular lymphoma

Interventions

Sponsors

Suzuki Kenta
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Histologically diagnosed as Grade 1, 2 or 3a FL according to WHO classification 2) Relapsed or refractory disease after receiving at least two prior systemic therapies 3) At least one measurable lesion according to the Lugano classification 4) ECOG PS of 0 to 1 5) Written informed consent

Exclusion criteria

Exclusion criteria: 1) Clinically or histologically suspected to be transformation from FL to an aggressive lymphoma or diagnosed as Grade 3b FL according to WHO classification 2) History of interstitial pneumonia or severe lung dysfunction 3) Received prior treatment with duvelisib (Patients who were refractory to PI3K inhibitors other than duvelisib or who experienced severe adverse events during treatment with the PI3K inhibitor were also excluded.) 4) Ongoing treatment for systemic bacterial, fungal, or viral infection 5) Administration of medications or foods that are strong inhibitors or inducers of CYP3A within 14 days of enrollment

Design outcomes

Primary

MeasureTime frame
Overall response rate

Contacts

Public ContactDevelopment Clinical

Yakult Honsha Co., Ltd.

clinical_development@yakult.co.jp+81-3-6625-8913

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026