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OncoMatch/Clinical Trials/NCT06300528

Pemigatinib in Patients With Relapsed or Refractory B-cell Non-Hodgkin Lymphomas

Is NCT06300528 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies Pemigatinib for relapsed or refractory b-cell non-hodgkin lymphoma.

Phase 2RecruitingUniversity of UtahNCT06300528Data as of Jun 2026

Treatment: PemigatinibThe purpose of this clinical trial is to learn if the study drug pemigatinib is effective in treating patients with relapsed or refractory B-cell non-Hodgkin lymphomas.

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Extracted eligibility criteria

Treatments studied

Targeted therapy

Pemigatinib

Cancer type

Non-Hodgkin Lymphoma

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

Min 2 prior lines

Cannot have received: fgfr inhibitor

Lab requirements

Blood counts

ANC ≥ 1000/mm3 independent of G-CSF support (no G-CSF within past 3 days), unless bone marrow involvement or splenomegaly with cytopenia (then ANC ≥ 750/mm3 allowed); Platelet count ≥ 75,000/mm3 independent of transfusion support (no transfusion within past 3 days), unless bone marrow involvement (then ≥ 50,000/mm3 allowed); Hemoglobin ≥ 8 g/dL independent of transfusion support (no transfusion within past 3 days), unless bone marrow involvement or splenomegaly with cytopenia (then ≥ 7 g/dL allowed); no evidence of myelodysplasia or hypoplastic bone marrow.

Kidney function

Estimated creatinine clearance ≥ 30 mL/min by Cockcroft-Gault formula.

Liver function

Total Bilirubin ≤ 1.5x institutional ULN or <2.5 x ULN with documented liver involvement and/or Gilbert's disease; AST(SGOT)/ALT(SGPT) ≤ 2.5 × institutional ULN; subjects with liver involvement allowed with AST and ALT ≤ 5 x ULN.

Cardiac function

No congestive heart failure NYHA Class III or IV, serious cardiac arrhythmias, unstable angina or acute coronary syndrome within 2 months, MI within 3 months, QTcF > 470 ms (unless corrected), LVEF < 40% in prior 12 months.

Adequate organ function as defined as: Hematologic: ANC ≥ 1000/mm3...; Platelet count ≥ 75,000/mm3...; Hemoglobin ≥ 8 g/dL...; Hepatic: Total Bilirubin ≤ 1.5x institutional ULN...; AST(SGOT)/ALT(SGPT) ≤ 2.5 × institutional ULN...; Renal: Estimated creatinine clearance ≥ 30 mL/min by Cockcroft-Gault formula.

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

US trial sites

  • Huntsman Cancer Institute at University of Utah · Salt Lake City, Utah

Showing up to 5 US sites.

See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT06300528 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior fgfr inhibitor 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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