GCT3013-02

Domaine de l’étude

Thérapeutique, Sécurité, Pharmacologie

Type d’étude

recherche interventionnelle

Critères d’inclusion: Vous pouvez participer si

1. Subject must sign an ICF
2. At least 18 years of age
3. Measurable disease defined as ≥1 measurable nodal lesion (long axis >1.5 cm and short axis >1.0 cm) or ≥1 measurable extra-nodal lesion (long axis >1.0 cm) on CT or MRI
4. ECOG PS score of 0 or 1
5. Acceptable organ function at screening
6. CD20-positive NHL at most recent representative tumor biopsy
7. If of childbearing potential subject must practicing a highly effective method of birth control
8. A man who is sexually active with a woman of childbearing potential must agree to use a barrier method of birth control
9. Arm 1: Newly diagnosed, previously untreated DLBCL (IPI>3)
Arm 2: R/R FL
Arm 3: Newly diagnosed, previously untreated FL grade 1-3A
Arm 4: R/R DLBCL and eligible for HDT-ASCT
Arm 5: R/R DLBCL ineligible for HDT-ASCT

Critères d’exclusion: Vous ne pouvez pas participer si

1. Chemotherapy, radiation therapy, or major surgery within 4 weeks prior to the first dose of epcoritamab
2. Treatment with CAR-T therapy within 30 days prior to first dose of epcoritamab
3. Clinically significant cardiac disease
4. Evidence of significant, uncontrolled concomitant diseases that could affect compliance with the protocol or interpretation of results
5. CNS lymphoma or known CNS involvement by lymphoma at screening as confirmed by MRI/CT scan of the brain and, if clinically indicated, by lumbar puncture
6. Active positive tests for hepatitis B virus or hepatitis C virus indicating acute or chronic infection
7. History of HIV antibody positivity, or tests positive for HIV at screening
8. Positive test results for HTLV-1
9. Suspected active or latent tuberculosis

• UZ Gent
• AZ Sint-Jan Campus Sint-Jan
• CHU UCL Namur - Site de Godinne