IKS03 for Advanced B Cell Non-Hodgkin Lymphomas

This study is testing a new treatment called IKS03 for people with advanced B-cell Non-Hodgkin Lymphoma (a type of cancer that starts in white blood cells). IKS03 is an antibody-drug conjugate, meaning it's designed to specifically target cancer cells. You might be able to join if you are 18 or older and have certain types of B-cell Non-Hodgkin Lymphoma, including Diffuse Large B Cell Lymphoma or Follicular Lymphoma. The study aims to find the safest and most effective dose of IKS03 and see how well it shrinks tumors. The study plans to enroll 140 participants. The current status of the study is unclear.

Study design
This is a two-part study: first, a dose-escalation phase to find the right dose, and then a dose-expansion phase to further evaluate safety and effectiveness. It is an interventional study, meaning participants will receive the study drug.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
The study will measure the recommended dose for expansion for up to 20 months and the objective response rate for up to 42 months.

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NCT05365659

IKS03 in Patients With Advanced B Cell Non-Hodgkin Lymphomas

Recruiting
PHASE1Ages 18+InterventionalTreatment
Iksuda Therapeutics Ltd.
~140 participants
Updated 2026-07-29 on ClinicalTrials.gov
What's tested:IKS03

At a glance

Recruiting sites
12 of 13 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Recommended Phase 2 Dose (Part I)
Measured over Up to 20 months
+1 more outcome measured
B-cell Non-Hodgkin Lymphoma
Diffuse Large B Cell Lymphoma
Follicular Lymphoma
Mantle Cell Lymphoma
B-cell Lymphoma
13 sites across 8 states
Italy4
Spain3
Maryland1
New South Wales1
South Australia1
Tasmania1
Western Australia1
Quebec1
  • Debra Wood, MD · STUDY_DIRECTOR · Iksuda Therapeutics

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  • Recommended Phase 2 Dose (Part I)Up to 20 months

    RP2D will be determined using dose limiting toxicities (DLTs) and all other available study data

  • Objective Response Rate (Part II)up to 42 months

    Antineoplastic effects will be assessed by Criteria for Response Assessment: The Lugano Classification (Cheson 2014)