RecruitingPhase 2NCT04984837

Study of Lacutamab in Peripheral T-cell Lymphoma

A Randomized Non Comparative Phase II Study of Lacutamab With GemOx Versus GemOx Alone in Relapsed/Refractory Patients With Peripheral T-cell Lymphoma


Sponsor

The Lymphoma Academic Research Organisation

Enrollment

56 participants

Start Date

Oct 5, 2021

Study Type

INTERVENTIONAL

Conditions

Summary

This is an open-label multicenter randomized non comparative phase II study to evaluate the safety and efficacy of the monoclonal anti-KIR3DL2 antibody Lacutamab in patients with Refractory/Relapsing (R/R) KIR3DL2 positive Peripheral T Cell Lymphoma (PTCL) : Not Other Specified (NOS), PTCL-TFH (including Angioimmunoblastic T-cell Lymphoma (AITL), Follicular T-cell lymphoma, Nodal peripheral T-cell lymphoma with TFH phenotype), Anaplastic large cell lymphoma (ALCL), Adult T-cell leukemia/lymphoma (ATL), Hepatosplenic T-cell lymphoma (HSTL), Enteropathy-associated T-cell lymphoma (EATL), Monomorphic epitheliotropic intestinal T cell lymphoma (MEITL), NK-T cell lymphoma (NKT) and Aggressive NK-cell leukemia (ANKL). The design is non comparative meaning that non comparison between arms will be performed as the control arm will ensure that the assumptions used for sample size calculation are verified. For that reason, randomization is unbalanced in favor of the experimental arm (2:1).


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a new drug called lacutamab in people with peripheral T-cell lymphoma (PTCL) — a rare and aggressive type of blood cancer. Lacutamab targets a protein called KIR3DL2 found on the surface of certain cancer cells. **You may be eligible if...** - You are 18 or older - You have a confirmed diagnosis of PTCL (various subtypes are eligible, including PTCL-NOS, AITL, ALCL, and others) - Your tumor cells test positive for the KIR3DL2 protein - Your cancer has come back or stopped responding after at least one, but no more than two, prior treatment regimens - You are in reasonable health (ECOG performance status 0–2) **You may NOT be eligible if...** - Your tumor does not express the KIR3DL2 protein - You have had more than two prior lines of treatment - Your PTCL subtype is not covered by study criteria - You have serious active infections or uncontrolled medical problems Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGLacutamab

750 mg/IV

DRUGGemcitabine

1000 mg/m²

DRUGOxaliplatine

100 mg/m²


Locations(64)

Institut Jules Bordet

Anderlecht, Belgium

VZW ZAS

Antwerp, Belgium

A. Z. Sint-Jan

Bruges, Belgium

Cliniques Universitaires de Bruxelles - Hôpital Erasme

Brussels, Belgium

Cliniques universitaires Saint-Luc - Université catholique de Louvain

Brussels, Belgium

Grand Hôpital de Charleroi

Charleroi, Belgium

UZ Antwerpen

Edegem, Belgium

HELORA - Hôpital de La LouvièreSite Jolimont

Haine-Saint-Paul, Belgium

CHU de LIEGE - Domaine Sart Tilman

Liège, Belgium

Clinique CHC MontLégia

Liège, Belgium

CHR Verviers

Verviers, Belgium

CHU Dinant Godinne - UCL Namur - YVOIR

Yvoir, Belgium

CHU de Nancy - Brabois

Nancy, France, France

CHU d'Amiens

Amiens, France

CHU d'Angers

Angers, France

CH d Avignon - Hopital Henri Duffaut

Avignon, France

CH de la Côte Basque - Hôpital de Bayonne

Bayonne, France

Institut Bergonié

Bordeaux, France

CHU de Caen - Côte de Nacre - IHBN

Caen, France

CH Métropole Savoie

Chambéry, France

CHU de Clermont Ferrand - Estaing

Clermont-Ferrand, France

APHP - Hôpital Henri Mondor

Créteil, France

CHU de Dijon BOURGOGNE - Hôpital François Mitterand

Dijon, France

CH de Dunkerque

Dunkirk, France

CHD de Vendée

La Roche-sur-Yon, France

CHU de Grenoble - Hôpital Albert Michallon

La Tronche, France

Ch de Versailles - Hopital Andre Mignot

Le Chesnay, France

CH du Mans

Le Mans, France

CHRU de Lille - Hôpital Claude Hurriez

Lille, France

Hôpital Saint Vincent-De-Paul

Lille, France

Chu de Limoges - Hopital Dupuytren

Limoges, France

Centre Leon Berard

Lyon, France

Chu de Meaux

Meaux, France

CHU de Montpellier

Montpellier, France

CH de Mulhouse

Mulhouse, France

CHU de Nantes - Hôtel Dieu

Nantes, France

CHU de Nîmes

Nîmes, France

CHR d'Orléans

Orléans, France

APHP - Hopital Necker

Paris, France

APHP - Hôpital de la Pitié Salpétrière

Paris, France

APHP - Hôpital Saint Antoine

Paris, France

APHP - Hôpital Saint Louis

Paris, France

CH de Perpignan

Perpignan, France

CHU de Bordeaux - Hôpital Haut Lévêque - Centre François Magendie

Pessac, France

CH de Périgueux

Périgueux, France

Centre Hospitalier Lyon Sud

Pierre-Bénite, France

CHU de Poitiers - Hôpital de La Milétrie

Poitiers, France

Centre Hospitalier Annecy Genevois

Pringy, France

CHU de Reims

Reims, France

CHU de Rennes - Hôpital de Pontchaillou

Rennes, France

Centre Henri Becquerel

Rouen, France

Institut de Cancérologie et d'Hématologie Universitaire de Saint-Étienne

Saint-Etienne, France

Institut de Cancerologie Strasbourg Europe

Strasbourg, France

Institut Universitaire du Cancer de Toulouse - Oncopole

Toulouse, France

CH de Bretagne Atlantique - Hopital Chubert

Vannes, France

Charite Universitat Smedizin Berlin

Berlin, Germany

GEORG-AUGUST-UNIV, GOETTINGEN - Klinik fur Haematologie und Medizini

Goettigen, Germany

Universitatsklinikum Halle (Saale)

Halle, Germany

UNIVERSITAT LEIPZIG - Klinik fur Hamatologie, Zelltherapie und Hamostaseo

Leipzig, Germany

UNIVERSITATSKLINIKUM REGENSBURG - Klinik für Innere Medizin III

Regensburg, Germany

Hospital Universitari Vall d'Hebron

Barcelona, Spain

Hospital Universitario Fundacion Jimenez Diaz - Hematologia

Madrid, Spain

Hospital Universitario Marqués de Valdecilla

Santander, Spain

Hospital Clínico Universitario de Valencia

Valencia, Spain

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NCT04984837


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