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OncoMatch/Clinical Trials/NCT06522737

A Study of Duvelisib Versus Gemcitabine or Bendamustine in Participants With Relapsed/Refractory Nodal T Cell Lymphoma With T Follicular Helper (TFH) Phenotype

Is NCT06522737 recruiting? Yes, currently enrolling (Jun 2026). This Phase 3 trial studies multiple treatments including Duvelisib and Gemcitabine for lymphoma.

Phase 3RecruitingSecuraBioNCT06522737Data as of Jun 2026Location: International · 10 countries

Treatment: Duvelisib · Gemcitabine · BendamustineThe study will evaluate the progression-free survival benefit of duvelisib monotherapy as compared to investigator's choice of gemcitabine or bendamustine in participants with relapsed/refractory nodal T cell lymphoma with TFH phenotype.

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Extracted eligibility criteria

Treatments studied

Chemotherapy

GemcitabineBendamustine

Other

Duvelisib

Cancer type

Non-Hodgkin Lymphoma

Hodgkin Lymphoma

Prior therapy

Min 1 prior line

Must have received: cytotoxic chemotherapy

Relapsed or refractory to at least 1 prior systemic, cytotoxic therapy for T cell lymphoma.

Cannot have received: phosphoinositide-3-kinase (PI3K) inhibitor

Received prior treatment with a phosphoinositide-3-kinase (PI3K) inhibitor.

Cannot have received: allogeneic transplant

Received prior allogeneic transplant any time in the past

Cannot have received: autologous transplant

Exception: within 60 days prior to the first dose of study drug

received autologous transplant within 60 days prior to the first dose of study drug

Cannot have received: gemcitabine (gemcitabine)

Exception: within 60 days prior to the first dose of study drug

Prior exposure to planned study treatment investigator's choice therapy (gemcitabine or bendamustine) within 60 days prior to the first dose of study drug.

Cannot have received: bendamustine (bendamustine)

Exception: within 60 days prior to the first dose of study drug

Prior exposure to planned study treatment investigator's choice therapy (gemcitabine or bendamustine) within 60 days prior to the first dose of study drug.

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT06522737 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior phosphoinositide-3-kinase (PI3K) inhibitor, allogeneic transplant, autologous transplant disqualifies patients from enrollment.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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