NCT02896582CompletedPhase 2
Efficacy of Upfront and Maintenance Obinutuzumab in Mantle Cell Lymphoma Treated by DHAP and MRD Driven Maintenance
Phase II Study to Evaluate the Efficacy of Upfront Obinutuzumab in Mantle Cell Lymphoma Patients Treated by DHAP Followed by Autologous Transplantation Plus Obinutuzumab Maintenance Then MRD Driven Maintenance
Source: ClinicalTrials.gov · Last updated 14 Jan 2026
Brief summary (registry, in English)
This study is a multicentric, single arm phase II trial to evaluate the efficacy of upfront obinutuzumab in mantle cell lymphoma patients treated by Cisplatinum-Cytarabine-Dexamethasone (DHAP) followed by autologous transplantation plus obinutuzumab maintenance then Molecular Residual Disease (MRD) driven maintenance
- Status (registry)
- Completed
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 86 (actual)
- First submitted
- 6 Sept 2016
- Start date
- 29 Nov 2016
- Primary completion date
- Mar 2019
- Lead sponsor
- The Lymphoma Academic Research Organisation
- Diseases
- Mantle cell lymphoma
- NCT number
- NCT02896582
What you commit to
- Study type: Interventional · Phase 2
- Participants enrolled: 86
- From 29 Nov 2016 to the primary completion date, Mar 2019
- 30 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Patients with a malignancy that has been treated but not with curative intent, unless the malignancy has been in remission without treatment for ≥ 5 years prior to enrollment. Patients with a history of curatively treated basal or squamous cell carcinoma or melanoma of the skin or in situ carcinoma of the cervix are eligible.
- Prior history of Progressive Multifocal Leukoencephalopathy (PML)
- Vaccination with a live vaccine a minimum of 28 days prior to inclusion (Prolonged B cell depletion)
Other illness
- Severe cardiac disease: York Heart Association (NYHA) grade 3-4
- History of chronic liver disease
- Hepatic veno-occlusive disease or sinusoidal obstruction syndrome
- Known seropositivity for Human Immunodeficiency Virus (HIV), Hepatitis C Virus (HCV) or other active infection uncontrolled by treatment.
- Viral infection with hepatitis B virus (HBV) defined as hepatitis B surface antigen (HBsAg) positive and/or Hepatitis B core antibody (anti-HBc) positive Note: Patients who are immune due to hepatitis B vaccination or natural infection (HBs Ag and anti-HBc negative, anti-HBs positive) are eligible. But the patients who are immune due to hepatitis B natural infection should consult liver disease experts before start of treatment and should be monitored and managed following local medical standards to prevent hepatitis reactivation
- History of severe allergic or anaphylactic reactions to humanized or murine monoclonal antibodies. Known sensitivity or allergy to murine products
- Psychiatric illness or condition which could interfere with their ability to understand the requirements of the study.
Lab values
- Impaired liver (ALanine Amino Transferase (ALAT)/ASparagin Amino Transferase (ASAT) ≥ 2.5 Upper Limit of Normal (ULN), bilirubin ≥ 1.5 ULN), renal (calculated creatinine clearance \< 50 ml/min) or other organ function which will interfere with the treatment, if not related to lymphoma.
- Any of the following laboratory abnormalities, if not result of a BM infiltration:
- Absolute Neutrophils Count (ANC) \<1,500 /mm3 (1.5 x 109/L)
- Platelet counts \< 75,000/mm3 (75 x 109/L)
Age
- surgically sterile or ≥ 2 years after the onset of menopause
Other
- Pregnancy/Nursing mothers
- Fertile men or women of childbearing potential unless:
- willing to use a highly effective contraceptive method
- Person deprived of his/her liberty by a judicial or administrative decision
- Person hospitalized without consent
- Adult person under legal protection
Who the study is looking for
- Age ≥ 18 and age ≤ 65
- Histologically confirmed (according to the World Health Organization (WHO) classification) mantle cell lymphoma. The diagnosis has to be confirmed by phenotypic expression of CD5, CD20 and cyclin D1 or the t(11;14) translocation.
- Bone marrow aspiration performed at inclusion for MRD analyses
- Eligible for autologous stem cell transplant
- Previously untreated MCL
- Stage Ann Arbor II-IV in need of treatment
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 - 2
- Life expectancy of more than 3 months
- Written informed consent
- Patient affiliated by any social security system
Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers
Sites (30)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| CHU D'amiens Coordinator of this site? Confirm its status | Amiens | France | Unknown status |
| CHU d Angers Coordinator of this site? Confirm its status | Angers | France | Unknown status |
| CH d'Avignon Coordinator of this site? Confirm its status | Avignon | France | Unknown status |
| CHU de CAEN Coordinator of this site? Confirm its status | Caen | France | Unknown status |
| CHU de Clermont-Ferrand Coordinator of this site? Confirm its status | Clermont-Ferrand | France | Unknown status |
| Hopital Henri Mondor Coordinator of this site? Confirm its status | Créteil | France | Unknown status |
| CHU de Dijon - Hôpital le Bocage Coordinator of this site? Confirm its status | Dijon | France | Unknown status |
| CHU de Grenoble Coordinator of this site? Confirm its status | Grenoble | France | Unknown status |
| CHD Vendée Coordinator of this site? Confirm its status | La Roche-sur-Yon | France | Unknown status |
| Clinique Victor Hugo Coordinator of this site? Confirm its status | Le Mans | France | Unknown status |
| Chru Lille - Hopital Claude Huriez Coordinator of this site? Confirm its status | Lille | France | Unknown status |
| CHU Limoges Coordinator of this site? Confirm its status | Limoges | France | Unknown status |
| CHU Montpellier Coordinator of this site? Confirm its status | Montpellier | France | Unknown status |
| CHU Nantes Coordinator of this site? Confirm its status | Nantes | France | Unknown status |
| APHP - Hôpital Necker Coordinator of this site? Confirm its status | Paris | France | Unknown status |
| Hopital Saint Louis Coordinator of this site? Confirm its status | Paris | France | Unknown status |
| Ch Perpignan Coordinator of this site? Confirm its status | Perpignan | France | Unknown status |
| CHU de Haut Leveque Coordinator of this site? Confirm its status | Pessac | France | Unknown status |
| CHU Lyon Sud Coordinator of this site? Confirm its status | Pierre-Bénite | France | Unknown status |
| CHU de Poitiers Coordinator of this site? Confirm its status | Poitiers | France | Unknown status |
| Centre Hospitalier Annecy Genevois Coordinator of this site? Confirm its status | Pringy | France | Unknown status |
| CHU Robert Debré Coordinator of this site? Confirm its status | Reims | France | Unknown status |
| CHU Pontchaillou Coordinator of this site? Confirm its status | Rennes | France | Unknown status |
| Centre Henri Becquerel Coordinator of this site? Confirm its status | Rouen | France | Unknown status |
| Institut de Cancérologie de Loire Coordinator of this site? Confirm its status | Saint-Priest-en-Jarez | France | Unknown status |
| CHU de Strasbourg Coordinator of this site? Confirm its status | Strasbourg | France | Unknown status |
| I.U.C.T Oncopole Coordinator of this site? Confirm its status | Toulouse | France | Unknown status |
| CHRU Bretonneau Coordinator of this site? Confirm its status | Tours | France | Unknown status |
| CHU de Brabois Coordinator of this site? Confirm its status | Vandœuvre-lès-Nancy | France | Unknown status |
| Gustave Roussy Cancer Campus Coordinator of this site? Confirm its status | Villejuif | France | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.