OncoMatch

OncoMatch/Clinical Trials/NCT06088654

Phase1/2 Study of IPH6501 in Patients With Relapsed /Refractory B-Cell Non-Hodgkin Lymphoma

Is NCT06088654 recruiting? Yes, currently enrolling (May 2026). This Phase 1/2 trial studies IPH6501 for non hodgkin lymphoma.

Phase 1/2RecruitingInnate PharmaNCT06088654Data as of May 2026

Treatment: IPH6501This is an international, first-in-human, multicenter, open-label Phase 1/2 study to evaluate the safety profile, tolerability of IPH6501, and determine the recommended phase 2 dose (RP2D) for patients with B-Cell non-Hodgkin lymphoma.

Check if I qualify

Extracted eligibility criteria

Cancer type

Hodgkin Lymphoma

Non-Hodgkin Lymphoma

Biomarker criteria

Required: CD20 overexpression (CD20+)

CD20+ B-cell non-Hodgkin's lymphoma

Performance status

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

Prior therapy

Min 2 prior lines

Must have received: anti-CD20 antibody therapy (rituximab)

at a minimum anti-CD20 antibody therapy (e.g., rituximab) potentially in combination with chemotherapy

Cannot have received: chemotherapy

Exception: within less than 4 weeks before study drug administration

Prior chemotherapy, immunotherapy or other anti-cancer therapy within less than 4 weeks before study drug administration.

Cannot have received: immunotherapy

Exception: within less than 4 weeks before study drug administration

Prior chemotherapy, immunotherapy or other anti-cancer therapy within less than 4 weeks before study drug administration.

Cannot have received: anti-cancer therapy

Exception: within less than 4 weeks before study drug administration

Prior chemotherapy, immunotherapy or other anti-cancer therapy within less than 4 weeks before study drug administration.

Cannot have received: autologous stem cell transplant

Exception: within 100 days prior to first dose of study drug

Autologous stem cell transplant ... within 100 days prior to first dose of study drug

Cannot have received: CAR-T cell therapy

Exception: within 100 days prior to first dose of study drug

treatment with CAR-T (Chimeric Antigen Receptor T-Cell) cell therapy within 100 days prior to first dose of study drug

Lab requirements

Blood counts

Kidney function

Liver function

Adequate organ and hematological function

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

US trial sites

  • City of Hope · Duarte, California
  • Cedars Sinai · Los Angeles, California
  • Siteman Cancer Center · St Louis, Missouri
  • Icahn School Of Medicine At Mount Sinai · New York, New York
  • Memorial Sloan Kettering Cancer Center · New York, New York

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

Could you qualify for this trial?

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

Check if I qualify