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Completed Phase 2 Interventional

IPH4102/Lacutamab Alone or in Combination With Chemotherapy in Patients With Advanced T Cell Lymphoma

ClinicalTrials.gov ID: NCT03902184

Public ClinicalTrials.gov record NCT03902184. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 19, 2026, 11:12 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

TELLOMAK: T-cell Lymphoma Anti-KIR3DL2 Therapy. An Open Label, Multicohort, Multi-center Phase II Study Evaluating the Efficacy and Safety of IPH4102 Alone or in Combination With Chemotherapy in Patients With Advanced T-cell Lymphoma

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is an open label, multi-cohort, and multi-center phase II study, which evaluates the clinical activity and safety of IPH4102 in Sezary Syndrome and Mycosis fungoides as single agent.

Study identification

NCT ID
NCT03902184
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Innate Pharma
Industry
Enrollment
170 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 22, 2019 (Actual)
Primary completion
Jan 8, 2026 (Actual)
Completion
Jan 8, 2026 (Actual)
Last update posted
Apr 29, 2026

2019 – 2026

United States locations

U.S. sites
17
U.S. states
11
U.S. cities
15
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35294 —
University of California, Los Angeles (UCLA) - Medical Center Los Angeles California 90095 —
Irvine Medical Center Orange California 92868 —
Stanford University Stanford California 94305 —
Moffitt Cancer Center Tampa Florida 33612 —
University of South Florida Tampa Florida 33612 —
Northwestern University The Feinberg School of Medicine Chicago Illinois 60611 —
Dana-Farber Cancer Institute Boston Massachusetts 02215 —
Washington University School of Medicine St Louis Missouri 63110 —
Dartmouth Hitchcock Medical Center Lebanon New Hampshire 03756 —
Universal Dermatology, PLLC68 Fairport New York 14450 —
Columbia University Department of Dermatology New York New York 10032 —
University of Pennsylvania Philadelphia Pennsylvania 19104 —
Thomas Jefferson University Philadelphia Pennsylvania 19107 —
University of Pittsburgh School of Medicine Pittsburgh Pennsylvania 15208 —
MD Anderson Cancer Center Houston Texas 77030-4009 —
Inova Health Care Services Fairfax Virginia 22031 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 36 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03902184, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 29, 2026 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03902184 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →