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NCT06088654 · ClinicalTrials.gov registry record · Phase 1

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

A Phase 1 study of Non-Hodgkin Lymphoma, sponsored by Innate Pharma.

Recruiting
Registry status
Phase 1
Development phase
184
Enrollment target
14
Study locations

NCT06088654 is a Phase 1 study of Non-Hodgkin Lymphoma that is actively recruiting participants, run by Innate Pharma. The registered enrollment target is 184 participants, above the 150-participant average among 104 other Non-Hodgkin Lymphoma trials with a reported enrollment target (23% higher). The trial reports 14 study locations across 6 states.

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The verdict

NCT06088654, a Phase 1 study of Non-Hodgkin Lymphoma, is actively recruiting participants, sponsored by Innate Pharma.

RECRUITING
Registry status
Phase 1
Development phase
184 participants
Enrollment target
14
Study locations

Study Summary

This 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.

Conditions Studied

Interventions

  • DRUG IPH6501

Study Locations (14)

Other

  • Austin Health - Heidelberg
  • Institute Bergonie - Bordeaux
  • Centre Hospitalier Regional Universitaire de Lille - Lille
  • Hospices Civils de Lyon - Lyon
  • Hôpital de la Coception - Marseille
  • Centre Hospitalier Universitaire de Nantes - Nantes

California

  • City of Hope - Duarte
  • Cedars Sinai - Los Angeles

New York

  • Icahn School Of Medicine At Mount Sinai - New York
  • Memorial Sloan Kettering Cancer Center - New York

Victoria

  • Monash Health - Clayton
  • Peninsula Private Hospital - Frankston

Missouri

  • Siteman Cancer Center - St Louis

New South Wales

  • Wollongong Private Hospital - Wollongong

Trial Details

FieldValue
Enrollment Target 184 participants
Start Date 2024-03-04
Est. Completion 2028-12-31
Phase Phase 1

Sponsor

Innate Pharma

12 total trials

What the Registry Record Tells You About NCT06088654

The ClinicalTrials.gov registry entry for NCT06088654 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 184 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 150-participant average among 104 other Non-Hodgkin Lymphoma trials with a reported enrollment target (23% higher). The listed sponsor is Innate Pharma, which has 12 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Non-Hodgkin Lymphoma appearing as the primary indexed condition, and to 1 intervention - of which IPH6501 is the first listed.

NCT06088654 reports 14 study locations spanning 6 distinct geographic areas - top geographies include Other, California, New York.

Frequently Asked Questions

What is clinical trial NCT06088654 about?

NCT06088654 is a clinical study titled "Phase1/2 Study of IPH6501 in Patients With Relapsed /Refractory B-Cell Non-Hodgkin Lymphoma". This 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.

What is the current status of trial NCT06088654?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 184 participants. The study started on 2024-03-04. Estimated completion is 2028-12-31.

What conditions does trial NCT06088654 study?

This clinical trial studies the following conditions: Non-Hodgkin Lymphoma.

What interventions are being tested in trial NCT06088654?

The interventions under investigation include: IPH6501 (DRUG).

Who is sponsoring clinical trial NCT06088654?

This trial is sponsored by Innate Pharma, which has 12 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06088654 being conducted?

This trial has 14 study locations across California, Missouri, New York, New South Wales, Victoria. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.