OncoMatch

OncoMatch/Clinical Trials/NCT06911502

A Study to Compare the Efficacy and Safety of Golcadomide in Combination With Rituximab (Golca + R) vs Investigator's Choice in Participants With Relapsed/Refractory Follicular Lymphoma Who Have Received at Least 1 Prior Line of Systemic Therapy (GOLSEEK-4)

Is NCT06911502 recruiting? Yes, currently enrolling (Sep 2026). This Phase 3 trial studies multiple treatments for follicular lymphoma.

Phase 3RecruitingCelgeneNCT06911502Data as of Sep 2026Location: International · 21 countries

Treatment: Golcadomide · Rituximab · Lenalidomide · Cyclophosphamide · Doxorubicin · Vincristine · Prednisone/Prednisolone · BendamustineThe study is designed as a multicenter, randomized, open label Phase 3 study to compare the efficacy and safety of golcadomide in combination with rituximab vs investigator's choice in participants with relapsed/refractory follicular lymphoma who have received at least one line of prior systemic therapy.

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Extracted eligibility criteria

Treatments studied

Immunotherapy

Rituximab

Targeted therapy

Golcadomide

Chemotherapy

CyclophosphamideDoxorubicinVincristineBendamustine

Endocrine / hormonal

Lenalidomide

Other

Prednisone/Prednisolone

Cancer type

Non-Hodgkin Lymphoma

Performance status

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

Prior therapy

Min 1 prior line

Must have received: systemic therapy

Must have received: combination including an anti-cd20 monoclonal antibody and an alkylating agent (rituximab, obinutuzumab, cyclophosphamide, bendamustine)

Lab requirements

Blood counts

absolute neutrophil count (anc) ≥ 1,000 cells/mm3; platelet count ≥ 75,000 cells/mm3; hemoglobin ≥ 7.5 g/dl

Kidney function

estimated glomerular filtration rate (egfr) ≥ 30 ml/min/1.73m²

Liver function

serum aspartate transaminase (ast/sgot) or alanine transaminase (alt/sgpt) ≤ 2.5 x uln (≤ 5.0× uln if liver involvement); serum total bilirubin ≤ 1.5 × uln (≤ 3.0 × uln if liver involvement; ≤ 5.0 × uln for gilbert's syndrome)

Cardiac function

adequate cardiac function for anthracycline-based chemotherapy: lvef ≥ 45% by echo or muga

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

US trial sites

  • Local Institution - 0225 · Birmingham, Alabama
  • Infirmary Cancer Care · Mobile, Alabama
  • Alaska Oncology and Hematology · Anchorage, Alaska
  • Local Institution - 0215 · Little Rock, Arkansas
  • City of Hope Comprehensive Cancer Center · Duarte, California

Showing up to 5 US sites.

See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT06911502 currently recruiting?

Yes, this trial is currently recruiting patients.

Is prior treatment required for enrollment?

Yes. Patients must have previously received systemic therapy and combination including an anti-cd20 monoclonal antibody and an alkylating agent.

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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