Study of Safety and Efficacy of Betalutin and Rituximab in Patients With FL

• Status: Active, not recruiting
• Trial end date: 2025-06-01
• Target enrollment: 0
• Participant gender: All

Summary

This study is a Phase 1b, open-label, single arm dose escalation study of Betalutin followed by rituximab in patients with previously treated follicular lymphoma. The purpose of this study is to characterise the safety, tolerability, pharmacokinetics, pharmacodynamics and preliminary anti-tumour activity of Betalutin in combination with rituximab.

• Phase: Phase 1
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Nordic Nanovector
• Collaborator: ICON Clinical Research
• Treatments: Rituximab

Criteria

Inclusion Criteria:

• Patient must be ≥18 years at the time of signing the informed consent

• ECOG performance status of 0-2

• Histologically confirmed diagnosis (by 2008 World Health Organization [WHO] classification) of follicular lymphoma (grade 1, 2 or 3a)

• At least one (but not more than 3) prior regimens with an anti-CD20 antibody (alone or in combination with chemotherapy), with documented relapsed, refractory disease (must not be anti-CD20 antibody-refractory) or PD

• Presence of at least one bi-dimensionally measurable lesion by CT or MRI: longest diameter (LDi) >1.5 cm for a nodal lesion; LDi >1.0 cm for an extranodal lesion within 28 days prior to start of treatment

• Normal organ and bone marrow function defined as:

1. Absolute neutrophil count ≥1.5 x 109/L;

2. Platelet count ≥150 x 109/L;

3. Haemoglobin ≥9 g/dL;

4. Total bilirubin ≤1.5 x upper limit of normal (ULN) (except patients with documented Gilbert's syndrome [<3.0 mg/dL]);

5. Aspartate transaminase (AST); Alanine transaminase (ALT) or Alkaline phosphatase (ALP) ≤2.5 x ULN (or ≤5.0 x ULN if liver involvement by primary disease);

6. Adequate renal function as demonstrated by a serum creatinine within the upper limit of normal range

• Bone marrow involvement by lymphoma <25%

• Life expectancy >3 months

• Negative hepatitis B, hepatitis C and human immunodeficiency virus (HIV) screening tests

• Patients must agree to use effective contraception for 12 months following last study drug administration

Exclusion criteria:

• Previous haematopoietic stem cell transplantation (autologous and allogenic)

• Evidence of histological transformation from FL to DLBCL at time of screening.

• Previous total body irradiation

• Chemotherapy, immunotherapy or investigational therapy within 28 days before the start of study drug administration (corticosteroid treatment at doses of ≤20 mg/day, topical or inhaled corticosteroids, granulocyte colony-stimulating factor [G-CSF] or granulocyte-macrophage colony-stimulating factor [GM CSF] are permitted up to 2 weeks prior to start of study treatment) or failure to recover from AEs associated with prior treatment

• Previous treatment with radioimmunotherapy

• Patients who are receiving any other investigational medicinal products

• Known or suspected central nervous system (CNS) involvement of lymphoma

• History of a previous treated cancer except for the following:

1. adequately treated local basal cell or squamous cell carcinoma of the skin

2. cervical carcinoma in situ

3. superficial bladder cancer or localised prostate cancer undergoing surveillance or surgery

4. localised breast cancer treated with surgery and radiotherapy but not including systemic chemotherapy

5. other adequately treated Stage 1 or 2 cancer currently in CR

• Pregnant or lactating women

• Exposure to another CD37 targeting drug

• A known hypersensitivity to RTX, lilotomab, Betalutin or murine proteins or any excipient used in RTX, lilotomab or Betalutin

• Receipt of live, attenuated vaccine within 30 days prior to enrolment

• Evidence of severe or uncontrolled systemic diseases (e.g. ongoing infection, respiratory, cardiac, hepatic or psychiatric conditions) which in the Investigator's opinion would compromise the protocol objectives