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Clinical Trials in France / NCT06186648
Recruiting Phase 2

Evaluation of Treatment by Glofitamab in Combination With Rituximab or Obinutuzumab Plus CHOP in Patients With RIchter Syndrome

NCT06186648 · tracked via the Priya Life Science France tracker
Phase
Phase 2
Started
2024-03-21
Last updated
2026-06-30

Condition(s) studied

Richter Syndrome

Investigational drug(s) / intervention(s)

Glofitamab + ObinutuzumabAll Glofitamab trials (47) →All Obinutuzumab trials (91) →

Glofitamab + Obinutuzumab: Duration of each cycle is 21 days. Cycle 1: R-CHOP Cycle 2: G-CHOP + glofitamab (at this cycle onnly, Obinutuzumab will be injected instead of Rituximab in order to decreased the risk of cytokine released syndrome) Cycle 3-6: R-CHOP + glofitamab Cycle 7-8: glofitamab alone

Study summary

This is a national clinical trial, multicentric (28 centers), non-randomized phase 2 study.

Population: Patients with previously untreated Richter's syndrome (RS), defined as the occurrence of an aggressive lymphoma (of diffuse large B-cell lymphoma histology) in a patient with chronic lymphocytic leukemia (CLL).

Study treatment:

The duration of each cycle is 21 days.

Cycle 1:

Participants will receive standard of care doses of R-CHOP in cycle 1 as follows:

* Rituximab 375 mg/m² IV Day 1
* Cyclophosphamide 750 mg/m² IV Day 1
* Doxorubicin 50 mg/m² IV Day 1
* Vincristine 1.4 mg/m² \[capped at 2.0 mg\] IV Day 1
* Prednisone 60 mg/m2 per day PO Day 1-5

Cycle 2:

In order to minimize cytokine release syndrome (CRS), participants will then receive G-CHOP as cycle 2 (with obinutuzumab) and glofitamab:

* Obinutuzumab 1000 mg single dose IV Day 1
* Cyclophosphamide 750 mg/m² IV Day 1
* Doxorubicin 50 mg/m² IV Day 1
* Vincristine 1.4 mg/m² \[capped at 2.0 mg\] IV Day 1
* Prednisone 60 mg/m2 per day PO Day 1-5
* Glofitamab : administered intravenously (IV) as a step-up dose on Days 8 (2.5 mg) and 15 (10 mg)

Cycle 3-6:

Participants will receive standard of care doses of R-CHOP and Glofitamab as follows:

* Rituximab 375 mg/m² IV Day 1
* Cyclophosphamide 750 mg/m² IV Day 1
* Doxorubicin 50 mg/m² IV Day 1
* Vincristine 1.4 mg/m² \[capped at 2.0 mg\] IV Day 1
* Prednisone 60 mg/m2 per day PO Day 1-5
* Glofitamab : 30 mg IV Day 8

Cycle 7 and 8 (only for patient in Complete Response or Partial response after Cycle 6):

Cycle 7 and 8 consist of 2 infusions of glofitamab only at D8C7 and D8C8:

● Glofitamab : 30 mg IV Day 8

Primary endpoint Percentage of participants with a complete response as assessed by the investigator using the Cheson IWG 2014 Lugano Classification (i.e. Deauville scale 1-3) after 6 cycles of R/G-CHOP + glofitamab or at permanent treatment discontinuation.

End of treatment is defined as after 6 cycles of R/G-CHOP + glofitamab. Permanent treatment discontinuation is defined as the discontinuation of all treatments (R/G-CHOP, glofitamab).

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Confirmed diagnosis of chronic lymphocytic leukemia or small lymphocytic lymphoma according to the revised iwCLL criteria with biopsy proven transformation to CD20 positive diffuse large B-cell lymphoma, consistent with RS according to the 2016 WHO classification 2. A fresh or archival tissue biopsy is mandatory 3. Previous therapy for CLL is allowed (but no prior therapy for RS) 4. Age greater than or equal to 18 years and less or equal to 80 years 5. ECOG performance status 0-2 6. Participants must have at least one measurable target lesion (≥ 1.5 cm) in its largest dimension by computed tomography (CT) scan. Measurable disease, defined as at least one bi-dimensionally measurable nodal or tumor lesion, defined as \> 1.5 cm in its longest dimension or PET-CT with at least one hypermetabolic lesion. Patients without measurable disease but with proven bone marrow infiltration by the RS are eligible. 7. Patients must meet the following hematologic criteria at screening, unless they have significant bone marrow involvement of either CLL or RS cells confirmed on biopsy: absolute neutrophil count ≥ 1.5 G/L, hemoglobin \>10 g/dL, and platelet count ≥75 G/L independent of transfusion within 7 days of screening 8. Subject must have adequate coagulation tests: Prothrombin Time \> 50%, Fibrinogen \> 1 g/L 9. Adequate liver function: Total bilirubin ≤ 1.5 x ULN; Aspartate aminotransferase (AST)/alanine aminotransferase (ALT) ≤ 3 x ULN 10. Adequate left ventricular ejection function (\> 50 %) 11. Adequate renal function: creatinine clearance calculated by MDRD/Cockcroft-Gault formula of ≥ 40 mL/min 12. Negative serologic or PCR test results for acute or chronic HBV infection 13. Negative test results for HCV and HIV (Patients who are positive for HCV antibody must be negative for HCV by PCR to be eligible for study participation) 14. Prior vaccination to the SARS-Cov-2 virus and and SARS-CoV-2 PCR testing and negative result before study treatment administration at each treatment cycle 15. Negative serum or urinary pregnancy test within 7 days prior to study treatment in women of childbearing potential. Patients must agree to either remain completely abstinent or to use two effective contraceptive methods\* until: * If the patient is a male: at least 3 months after pre-treatment with obinutuzumab or RCHOP or 2 months after the last dose of glofitamab, whichever is longer. Men must refrain from donating sperm during this same period * If patient is a female of childbearing potential: until at least 18 months after pre-treatment with obinutuzumab or RCHOP or 2 months after the last dose of glofitamab, whichever is longer 16. Ability to understand and the willingness to sign a written informed consent document. Patient must be willing and able to comply with protocol-mandated hospitalization upon administration of the first dose of glofitamab. Patient must also be willing to comply with all study-related procedures 17. Signed written informed consent 18. Patient covered by any social security system Exclusion Criteria: 1. Patients with the Hodgkin variant of RS 2. Patients with previously treated for RS 3. Current or past history or presence of clinically relevant disorder affecting the central nervous system (CNS) 4. Ineligible to CHOP full dose for any reason 5. Previous treatment with a bispecific antibody 6. Current or past history of DLBCL in the CNS (confirmed by CSF analysis) 7. Steroids treatment (\> 1 mg/kg/d for one week) before inclusion 8. History of anaphylactic reactions to human, chimeric, or mouse monoclonal antibodies or to any components of the product. 9. Prior allogeneic HSCT 10. Patients with known acute infection or reactivation of a latent infection, whether bacterial, viral (including, but not limited to, EBV, cytomegalovirus (CMV), hepatitis B, hepatitis C, HIV and SARS-CoV-2), fungal, mycobacterial, or other pathogens (excluding fungal infections of nail beds) or any major episode of infection requiring hospitalization or treatment with IV antibiotics (for IV antibiotics this pertains to completion of last course of antibiotic treatment) within 4 weeks prior to the first study treatment. 11. History of other malignancies, except: i) malignancy treated with curative intent and with no recurrence over the last 3 years ii) adequately treated non-melanoma skin cancer without evidence of disease iii) adequately treated carcinoma in situ without evidence of disease 12. Prior solid organ transplantation 13. History of treatment-emergent immune-related adverse events associated with prior immunotherapeutic agents, as follows: * Grade ≥ 3 adverse events with the exception of Grade 3 endocrinopathy managed with replacement therapy * Grade 1-2 adverse events that did not resolve to baseline after treatment discontinuation 14. Current uncontrolled autoimmune disease\* 15. History of human immunodeficiency virus 16. Hepatitis B or C seropositivity (unless clearly due to vaccination) 17. Pregnant or breastfeeding women 18. Unwilling or unable to participate in all required study evaluations and procedures. 19. Unable to understand the purpose and risks of the study and to provide a signed and dated informed consent form and authorization to use protected health information (in accordance with national and local subject privacy regulations) 20. Persons deprived of their liberty by judicial or administrative decision, persons subject to a legal protection measure (guardianship, curatorship, legal protection), persons under psychiatric care 21. Fertile male patients who cannot or do not wish to use an effective method of contraception, during and for 12 months after the final treatment used for the purposes of the study. 22. Patients with history of macrophage activation syndrome (MAS) / hemophagocytic lymphohistiocytosis (HLH) 23. LVEF \< 50% as determined by echocardiography or multiple uptake gated acquisition (MUGA) scan, significant or extensive cardiovascular disease such as New York HeartAssociation Class III or IV cardiac disease or Objective Assessment Class C or D,myocardial infarction within the last 3 months, unstable arrhythmias, or unstable angina. 24. Abnormal screening laboratory values as defined as following: a) ALT (SGOT) and/or ALT (SGPT) and/or ALP ≥ 3 x upper limit of normal (ULN); b) Total bilirubin ≥ 1.5 x ULN, unless due to Gilbert's disease; c) Creatinine ≥ 2.0 x ULN or creatinine clearance \< 40 mL/min (calculated). 25. Patient with history of confirmed progressive multifocal leukoencephalopathy (PML) 26. History of severe allergic or anaphylactic reactions to monoclonal antibody therapy (or recombinant antibody-related fusion proteins) 27. Any other diseases, metabolic dysfunction, physical examination finding, or clinical laboratory finding giving reasonable suspicion of a disease or condition that would contraindicate the use of an investigational drug 28. Major surgery or significant traumatic injury \< 28 days prior to the obinutuzumab infusion (excluding biopsies) or anticipation of the need for major surgery during study treatment 29. Administration of a live, attenuated vaccine within 4 weeks before obinutuzumab infusion 30. Treatment with another investigational agent or participating in another trial within 30 days prior to entering the study 31. Clinically significant history of liver disease or cirrhosis 32. Pregnant or breast-feeding or intending to become pregnant during the study 33. No affiliation to social security 34. Inability to comply with protocol mandated hospitalization and restrictions.

Primary outcome measure(s)

Trial sites (23)

FacilityCityRegionStatus
Amiens-Picardie Chu Amiens France Not Yet Recruiting
Angers Chu Angers France Not Yet Recruiting
BAYONNE - CH de la Côte Basque - Hématologie Bayonne France Not Yet Recruiting
Clermont-Ferrand - Chu Estaing Clermont-Ferrand France Recruiting
Grenoble - CHUGA - Hématologie Clinique Grenoble France Not Yet Recruiting
LILLE GHICL - Hôpital Saint Vincent de Paul Lille France Not Yet Recruiting
LILLE CHU - Hôpital Claude Huriez Lille France Not Yet Recruiting
LIMOGES - CHU Dupuytren 1 Limoges France Not Yet Recruiting
LYON-Centre Léon Bérard Lyon France Not Yet Recruiting
MONTPELLIER - Hôpital Saint-Eloi - Hématologie Clinique Montpellier France Not Yet Recruiting
APHP - Hôpital Saint-Louis - Hématologie adultes Paris France Not Yet Recruiting
APHP - Hôpital Saint-Antoine - Hématologie et thérapie cellulaire Paris France Not Yet Recruiting
APHP - Hôpital Pitié Salpêtrière - Hématologie Paris France Recruiting
Bordeaux Pessac Pessac France Not Yet Recruiting
LYON HCL - CH Lyon Sud Pierre-Bénite France Recruiting
Reims Chu Reims France Not Yet Recruiting
RENNES - CHU Pontchaillou - Hématologie Clinique Rennes France Not Yet Recruiting
ROUEN - Centre Henri Becquerel - Service Hématologie Clinique Rouen France Recruiting
Strasbourg - Icans Strasbourg France Not Yet Recruiting
Toulouse - IUCT Oncopole - Service d'Hématologie Toulouse France Recruiting
TOURS - Hôpital Bretonneau Tours France Not Yet Recruiting
NANCY - CHU Brabois Vandœuvre-lès-Nancy France Not Yet Recruiting
VERSAILLES - Hôpital André Mignot Versailles France Recruiting

More French Innovative Leukemia Organisation trials in France

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06186648 on ClinicalTrials.gov ↗ ← All trials in France