- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07736950
A Study Comparing a New Drug (Surovatamig) With Standard Radiotherapy With or Without Rituximab in Adults With Limited Stage Nodal Follicular Lymphoma (RAZOR)
An ALLG International Randomised Phase III Trial of Surovatamig Versus Involved Site Radiotherapy With or Without Rituximab in Limited Stage Nodal Follicular Lymphoma
The goal of this clinical trial is to learn if surovatamig works better than standard of care involved-site radiotherapy (ISRT) with or without rituximab to treat patients with limited-stage follicular lymphoma. It will also learn about the safety of the drug.
The main questions it aims to answer is whether surovatamig can produce deeper and more durable responses, reduce the risk of disease relapse, and improve event-free survival.
Participants will:
1) Take surovatamig for 4 cycles. The first cycle will have a dose ramp up in 3 steps over a period of 14 days. Cycle 2-4 are for 28 days with drug administered every fortnight.
OR 2a) Undergo radiotherapy only for 3 weeks OR 2b) Radiotherapy + rituximab weekly for 6 doses (6 weeks)
Visit the clinic once every cycle, at the end of treatment, and be monitored every 3 months in year 1, every 6 months in year 2, and once a year from year 3-5 for checkups and tests.
Aperçu de l'étude
Statut
Les conditions
Description détaillée
What the study is about:
This study will evaluate whether surovatamig, a novel CD19 × CD3 bispecific T-cell engager, can improve outcomes for people with previously untreated, limited-stage nodal follicular lymphoma (FL). The trial will compare surovatamig with the current standard of care: involved-site radiotherapy (ISRT) with or without rituximab. The aim is to determine whether surovatamig can produce deeper and more durable responses, reduce the risk of disease relapse, and improve event-free survival.
Who is it for:
This study is for adults aged 18 years or older who have:
- Histologically confirmed classical follicular lymphoma (Grade 1-3a), Ann Arbor stage I or II nodal, non-bulky disease ( less or equal to 7 cm)
- PET-positive, measurable disease
- No prior lymphoma-directed therapy
Study details:
This is an international, Phase III randomised clinical trial. Participants will be randomised 1:1 on either Surovatamig (6 doses over 12 weeks with an additional triple step-up dosing schedule over 14 days for cycle 1) or to the standard of care treatment (Involved-Site Radiotherapy (24 Gy) with or without 6 doses of rituximab, according to each site's predefined standard). Participants will be followed up for 5 years after treatment to assess long-term outcomes.
A total of 138 participants will be enrolled across Australia, New Zealand, the United Kingdom, Ireland and Nordic countries.
What is hoped from it:
If successful, surovatamig could represent a new standard of care for patients with early-stage nodal follicular lymphoma that is highly effective, well-tolerated, non-radiation frontline option for patients with limited-stage FL.
Type d'étude
Inscription (Estimé)
Phase
- Phase 3
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
La description
Inclusion Criteria:
- Patients or their legally authorised representative must voluntarily sign and date an informed consent form (ICF), approved by a Human Research Ethics Committee (HREC), prior to the initiation of any screening or trial-specific procedures.
- Provide samples for optional genetic research that supports the Genomic Initiative.
- Are willing and able to comply with procedures required in this protocol.
- Age 18 years and older at the time of signing the informed consent form (ICF).
- Must have histologically confirmed classical follicular lymphoma (FL) (previously Grade 1 to 3a FL) at the most recent representative tumour biopsy based on the local pathology report, according to the 5th edition of the World Health Organization (WHO) Classification of Haematolymphoid Tumours.
- Must have Ann Arbor Stage I or II, nodal, non-bulky disease (maximum tumour diameter less than or equal to 7 cm).
- Previously untreated disease (no prior systemic lymphoma-directed therapies).
Has one or more target lesions:
- A positron emission tomography/computed tomography (PET/CT) scan demonstrating PET-positive lesion(s), and
- At least one measurable nodal lesion (long axis over 1.5 cm) or at least one measurable extra-nodal lesion (long axis over 1.0 cm) on computed tomography (CT) scan or magnetic resonance imaging (MRI).
- Eastern Cooperative Oncology Group (ECOG) performance status 0-2.
Patient must have adequate renal and liver function, unless values meeting the following criteria are related to lymphoma:
- Serum aspartate aminotransferase (AST) or alanine aminotransferase (ALT) less or equal to 3.0 × upper limit of normal (ULN)
- Total bilirubin less or equal to 1.5 × ULN; subjects with Gilbert's syndrome may have total bilirubin greater than 1.5 × ULN, but conjugated (direct) bilirubin must be less or equal to 2 × ULN
- Estimated creatinine clearance (CrCl) greater or equal to 45 mL/min (as calculated by the Cockcroft-Gault formula)
Patient must have adequate haematologic function:
- Absolute neutrophil count (ANC) greater or equal to 1.0 × 10^?/L
- Haemoglobin greater or equal to 8 g/dL
- Platelet count greater or equal to 75 × 10^?/L
- Patients of child-bearing potential must have a negative serum pregnancy test 10 to 14 days prior to randomisation and again within 24 hours prior to Cycle 1 Day 1 (C1D1). The pregnancy test must be sensitive to at least 25 mIU/mL.
- Women of child-bearing potential must agree to practise at least two protocol-specified methods of birth control, effective from 28 days prior to randomisation through at least 12 months after the last dose of trial drug. Female patients of non-child-bearing potential do not need to use birth control.
- Male patients who are sexually active with female partners of child-bearing potential must agree, from 28 days prior to randomisation through 12 months after the last dose of trial drug, to practise the protocol-specified contraception, particularly using a latex or synthetic condom every time they have sexual intercourse with a partner of reproductive potential, even if they have undergone a successful vasectomy.
Exclusion Criteria:
- Has a history of prior systemic or radiotherapy therapy for follicular lymphoma (FL).
- Has prior or current follicular large B-cell lymphoma (World Health Organization [WHO] 2022 classification), formerly follicular lymphoma Grade 3B (WHO 2016 classification), histologic transformation to diffuse large B-cell lymphoma (DLBCL) or other aggressive lymphomas.
- Known or suspected central nervous system (CNS) involvement at screening based on clinical presentation or imaging findings.
- A history of severe allergic or anaphylactic reactions to any component or excipient of AZD486.
- Has had major surgery within 14 days prior to the first dose of trial intervention (excluding biopsies) or anticipation of the need for major surgery during trial intervention.
Clinically significant cardiovascular disease, such as:
- Myocardial infarction within less or equal to 12 weeks or stroke within 6 months prior to randomisation
- Screening 12-lead electrocardiogram (ECG) showing a baseline QT interval as corrected by Frederica's formula (QTcF) over 480 msec
- The following conditions within 3 months prior to randomisation:
i. Uncontrolled unstable angina ii. New York Heart Association (NYHA) Class III-IV congestive heart failure iii. Uncontrolled life-threatening cardiac arrhythmia iv. Other clinically significant ECG abnormalities in the opinion of the investigator
- History or presence of clinically relevant CNS pathology (based on investigator assessment) such as epilepsy, seizure, paresis, aphasia, severe brain injuries, dementia, Parkinson's disease, cerebellar disease, organic brain syndrome, or psychosis.
- Active bacterial, viral, fungal, mycobacterial, parasitic, or other infection (excluding fungal infections of nail beds) requiring systemic therapy or antibiotics within 2 weeks prior to randomisation.
Human immunodeficiency virus (HIV) infection unless:
- Patients on effective antiretroviral therapy with undetectable viral load within 6 months prior to trial entry are eligible
- HIV ribonucleic acid (RNA) will be monitored during the trial as clinically indicated
Active hepatitis B infection (detectable hepatitis B virus [HBV] deoxyribonucleic acid (DNA) or hepatitis B surface antigen [HBsAg]).
- Patients who are hepatitis B core antibody [HBcAb] positive but HBV DNA and HBsAg negative are eligible and will undergo monthly monitoring
- Patients who received intravenous immunoglobulin [IVIG] may have false-positive HBcAb; if HBV DNA and HBsAg are negative, prophylaxis may be omitted but monitoring is required
- Active hepatitis C, defined by detectable hepatitis C RNA in plasma by polymerase chain reaction (PCR). Patients with resolved infection may participate if hepatitis C RNA is undetectable.
Received a live, attenuated vaccine within 28 days prior to initiation of trial treatment.
a. Patients must not receive live vaccines while receiving trial intervention and for at least 6 months after the last dose of surovatamig or rituximab, and until B-cell recovery is confirmed.
Active tuberculosis (TB) or history of completed treatment for active TB within the past 12 months.
a. Interferon-gamma release assay (IGRA) testing must be performed if TB is suspected.
- History of other prior malignancies, except defined low-risk cases.
- Current autoimmune disease requiring immunosuppressive therapy other than prednisolone less than 20 mg daily (or equivalent).
- Current seizure disorder requiring therapy (patients with history must have complete CNS workup).
- History of clinically significant medical or psychiatric conditions interfering with trial participation or safety.
- Participation in another clinical trial with an investigational product within the last 28 days or 5 half-lives.
- Female patient who is pregnant, breastfeeding, or planning pregnancy or egg donation during or 12 months after treatment.
- Male patients planning to father a child or donate sperm during or 12 months after treatment.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Comparateur actif: Arm A (Investigational arm): Surovatamig
This arm involves treatment with Surovatamig only with no radiotherapy. Treatment is in 3 phases. 1. Cycle 1 is a 14 day cycle including a triple step-up dosing: Day 1 of cycle 1: 0.09 mg, Day 4 of cycle 1: 0.27 mg, Day 8 of cycle 1: 1.0 mg. 2. Cycle 2-4 are 28 day cycles with a dose administered every 2 weeks: Cycles 2-4 (28-day cycle): Surovatamig treatment doses administered on days 1 and 15 of each cycle at 7.2mg. 3. At the end of cycle 4, patients will enter the post-treatment period. |
Surovatamig is supplied as a concentrate for solution for intravenous administration (2mg/mL).
|
|
Comparateur actif: Arm B1: Involved-Site Radiotherapy (ISRT) 24Gy
This arm is the standard of care (SOC): Involved-Site Radiotherapy (ISRT) at 24Gy and involves radiotherapy for 3 weeks.
|
24 Gray of ISRT
|
|
Comparateur actif: Arm B2: Involved-Site Radiotherapy (ISRT) 24Gy + rituximab x 6 cycles
This arm is another standard of care (SOC): Involved-Site Radiotherapy (ISRT) at 24Gy with 6 doses of rituximab administered weekly by intravenous (IV) at 375 mg/m^2. 1 week = 1 cycle.
|
Involved-Site Radiotherapy (ISRT) at 24Gy with 6 doses of rituximab administered weekly by intravenous (IV) at 375 mg/m^2. 1 week = 1 cycle.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Event Free Survival
Délai: Time from date of randomisation until disease progression until end of 5 year follow up.
|
Determined by Lugano 2014 Response Criteria and audit of medical records
|
Time from date of randomisation until disease progression until end of 5 year follow up.
|
|
Event Free Survival
Délai: Time from date of randomisation to death from any cause, initiation of new anti-lymphoma treatment or disease progression until end of 10 year follow up. Assessment will be performed at end of treatment, every 3 months in year 1, every 6 months in year 2
|
As determined by the Lugano 2014 Response Criteria and audit of medical records
|
Time from date of randomisation to death from any cause, initiation of new anti-lymphoma treatment or disease progression until end of 10 year follow up. Assessment will be performed at end of treatment, every 3 months in year 1, every 6 months in year 2
|
Collaborateurs et enquêteurs
Les enquêteurs
- Chercheur principal: Chan Cheah, Sir Charles Gairdner Hospital
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
- Tumeurs
- Maladies du système immunitaire
- Tumeurs par type histologique
- Maladies lymphatiques
- Troubles lymphoprolifératifs
- Troubles immunoprolifératifs
- Lymphome non hodgkinien
- Lymphome
- Maladies hémiques et lymphatiques
- Lymphome folliculaire
- Acides aminés, peptides et protéines
- Protéines
- Anticorps, monoclonal
- Anticorps
- Immunoglobulines
- Immunoprotéines
- Protéines sanguines
- Globulines sériques
- Globulines
- Anticorps, monoclonal et murin
- Rituximab
Autres numéros d'identification d'étude
- ALLG NHL45
- ACTRN12626000311358 (Identificateur de registre: Australian New Zealand Clinical Trials Registry (ANZCTR))
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Données/documents d'étude
-
Ensemble de données de participant individuel
Commentaires d'informations: Email: info@allg.org.au
Informations sur les médicaments et les dispositifs, documents d'étude
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produit fabriqué et exporté des États-Unis.
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