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A Study of CN1 in Combination With CN401 in Adult Patients With Relapsed/Refractory Lymphoid Malignancies

20 octobre 2022 mis à jour par: Curon Biopharmaceutical (Australia) Co Pty Ltd

An Open-label, Multi-centre, Phase I/II Study to Investigate the Safety, Tolerability, and Preliminary Efficacy of CN1 in Combination With CN401 in Adult Patients With Relapsed/Refractory Lymphoid Malignancies

The study is designed to investigate the safety, tolerability and preliminary efficacy in combination with CN1 and CN401 in adult patients with relapsed/refractory lymphoid malignancies.

Aperçu de l'étude

Description détaillée

This is an open-label, multi-center, phase I/II study. The study includes two study drugs CN1 and CN401 and will be conducted in two parts: phase 1 and phase 2.

Phase I: Dose-finding study for the assessment of dose limiting toxicities (DLTs) at 3 or more dose levels in patients with advanced lymphoid malignancies.

Phase II: Expansion study to evaluate the preliminary efficacy of CN1 in combination with CN401 at the RP2D in parallel patient cohorts grouped by non-Hodgkin's Lymphoma (NHL) subtype.

There will 9-18 patients enrolled in the Phase 1 portion of the study and 15- 60 patients will be enrolled in Phase 2 - dosing determined by Phase 1.

Type d'étude

Interventionnel

Inscription (Réel)

7

Phase

  • Phase 2
  • La phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

    • Victoria
      • Bentleigh, Victoria, Australie, 3168
        • Monash Health - Monash Medical Centre

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans et plus (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  1. Age ≥ 18 years on the day of signing informed consent.
  2. Based on pathology review at the local institution, using the most recent edition of the World Health Organization (WHO) Classification of Tumors of Hematopoietic and Lymphoid Tissues as guidance, leading to the diagnosis of one of the following diseases and their histological subtypes: PTCL, CTCL, and B-cell NHL.
  3. Patients must have relapsed or refractory disease after at least one prior systemic anti-tumor treatment.
  4. The patients enrolled in Phase II of the study should have received NOT more than five lines of prior systemic therapies.
  5. Patients must have at least one evaluable lesion per Lugano 2014 Criteria. Measurable lesions are defined as those that can be accurately measured in at least two dimensions with conventional techniques (positron emission tomography/Computed tomography [PET/CT], magnetic resonance imaging [MRI]) or as > 1.5 cm with spiral CT scan. Patients with non-measurable lesions but assessable diseases (e.g., marrow disease without other radiographically measurable diseases) may be enrolled on a case-by-case basis in discussion with the Sponsor.
  6. ECOG performance status 0 to 2.
  7. At least 3 months of expected survival.
  8. Adequate organ functions, further defined as:

    • Hemoglobin ≥ 9 g/dL.
    • Absolute neutrophil count (ANC) ≥ 1 × 10E+09/L.
    • Platelets ≥ 50 × 10E+09/L (patient without bone marrow [BM] involvement) and ≥ 30 × 10E+09/L (patient with BM involvement).
    • Total bilirubin ≤ 1.5 times the upper limit of normal (ULN).
    • Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 2.5 × ULN if known liver involvement. The ALT and AST should be ≤ 1.5 × ULN in absence of liver involvement/metastasis.
    • Serum creatinine ≤ 2.0 mg/dL or calculated creatinine clearance ≥ 50 mL/min (as calculated by the Cockcroft-Gault method).
    • Activated partial thromboplastin time (APTT) or international normalized ratio (INR) ≤ 1.5 × ULN (unless patient is receiving anticoagulants).

Exclusion Criteria:

  1. Received any anti-tumour treatment (i.e., chemotherapy, radiotherapy, immunotherapy, biologic therapy, endocrine therapy, etc.,) within four weeks (or five half-lives of the agent, whichever is shorter) prior to the first dose of study drugs, with the following exceptions:

    1. Palliative radiation therapy within 2 weeks.
    2. Oral small molecule targeted therapies within 2 weeks prior to the first dose of study drugs or within 5 half-lives of the drug, whichever is shorter.
    3. Herbal medications within 7 days prior to the first dose.
  2. Received other investigational agents (not yet approved by any regulatory agency) within four weeks prior to the first dose of any study drugs.
  3. Immunosuppressive medication > 10 mg prednisolone per day or equivalent within 14 days prior to the first dose of the study drug. Note: Use of immunosuppressive medications as prophylaxis in subjects with contrast allergies are acceptable. In addition, temporary uses of corticosteroids considered non-clinically significant may be approved on a case-by-case basis in discussion with the Sponsor.
  4. Known clinically active central nervous system (CNS) or meningeal involvement. In the absence of symptoms, investigation into CNS involvement is not required. Patients are eligible if metastases have been treated, patients are neurologically returned to baseline or neurologically stable for at least four weeks and not requiring steroid therapy for at least one week prior to Cycle 1 Day 1.
  5. Active infection and in current need of, or likely to need, intravenous (IV) anti-infective therapy.
  6. History of immunodeficiency, including history of any positive test result for human immunodeficiency virus (HIV) antibody.
  7. Patients who are known to be hepatitis B or C positive (positive HBsAg and/or detectable level of HBV DNA or positive HCV antibody).
  8. Active Epstein Barr virus (EBV) unrelated to underlying lymphoma (positive serology for anti-EBV VCA IgM antibody and negative for anti-EBV EBNA IgG antibody, or clinical manifestations and positive EBV polymerase chain reaction [PCR] consistent with active EBV infection).
  9. Active CMV (positive serology for anti-CMV IgM antibody, negative for anti-CMV IgG antibody, and positive CMV PCR with clinical manifestations consistent with active CMV infection) and requiring therapy.
  10. Current history of a serious uncontrolled medical disorder, metabolic dysfunction, physical examination findings, or clinical laboratory findings giving reasonable suspicion of a disease or condition that contraindicates use of an investigational drug or render the patient at high risk from treatment complications.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Non randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: A (CN1 0.5mg/kg and CN401 400mg)

Patients were administered with CN1, 0.5mg/kg, once every three week in combination with 400mg CN401 twice a day, fasted.

Dosage/Route of admin: CN1- Intravenous Infusion(IV); CN401- Tablet, Oral

Three to six patients are expected to be enrolled in each arm.

CN1(0.5mg/kg) will be administered on Day 1 of each cycle (once every three weeks) for up to 12 months and CN401(400mg) will be administered orally twice daily.
Expérimental: B (CN1 1mg/kg and CN401 600mg)

Patients were administered with CN1, 1mg/kg, once every three week in combination with 600mg CN401 twice a day, fasted.

Dosage/Route of admin: CN1- Intravenous Infusion(IV); CN401- Tablet, Oral

Three to six patients are expected to be enrolled in each arm

CN1(1mg/kg) will be administered on Day 1 of each cycle (once every three weeks) for up to 12 months and CN401(600mg) will be administered orally twice daily.
Expérimental: C (CN1 1mg/kg and CN401 800mg)

Patients were administered with CN1, 1mg/kg, once every three week in combination with 800mg CN401 twice a day, fasted.

Dosage/Route of admin: CN1- Intravenous Infusion(IV); CN401- Tablet, Oral

Three to six patients are expected to be enrolled in each arm

CN1(1mg/kg) will be administered on Day 1 of each cycle (once every three weeks) for up to 12 months and CN401(800mg) will be administered orally twice daily.
Expérimental: D (CN1 3mg/kg and CN401 800mg)

Patients were administered with CN1, 3mg/kg, once every three week in combination with 800mg CN401 twice a day, fasted.

Dosage/Route of admin: CN1- Intravenous Infusion(IV); CN401- Tablet, Oral

Three to six patients are expected to be enrolled in each arm

CN1(3mg/kg) will be administered on Day 1 of each cycle (once every three weeks) for up to 12 months and CN401(800mg) will be administered orally twice daily.
Expérimental: E (CN1 10mg/kg and CN401 800mg)

Patients were administered with CN1, 10mg/kg, once every three week in combination with 800mg CN401 twice a day, fasted.

Dosage/Route of admin: CN1- Intravenous Infusion(IV); CN401- Tablet, Oral

Three to six patients are expected to be enrolled in each arm

CN1(10mg/kg) will be administered on Day 1 of each cycle (once every three weeks) for up to 12 months and CN401(800mg) will be administered orally twice daily.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
To evaluate the safety and tolerability of CN1 in combination with CN401 in patients with relapsed/refractory lymphoid malignancies through Incidence of Treatment-Emergent Adverse Events as assessed by CTCAE v5.0
Délai: Measurements at Baseline till completion of last safety visit (270 days)
Number of participants with treatment-related adverse events as assessed by CTCAE v5.0
Measurements at Baseline till completion of last safety visit (270 days)
To determine maximum tolerated dose and/or Recommended Phase II Dose (RP2D) of CN1 in combination with CN401
Délai: DLT assessed within 21 days after the first dose
Measured by Incidence of dose limiting toxicities (DLT) during the first cycle of treatment with CN1 in combination with CN401.
DLT assessed within 21 days after the first dose
To assess the change in anti-tumor activity of CN1 in combination with CN401 through Objective Response Rate analysis
Délai: Baseline to End of the Treatment assessed up to an average of 1 year
Measured/determined by Objective Response Rate
Baseline to End of the Treatment assessed up to an average of 1 year

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
To further evaluate the safety and tolerability of CN1 in combination with CN401 in patients with relapsed/refractory lymphoid malignancies through Incidence of Treatment-Emergent Adverse Events as assessed by CTCAE v5.0
Délai: Measurements at Baseline till completion of last safety visit (270 days)
Number of participants with treatment-related adverse events as assessed by CTCAE v5.0
Measurements at Baseline till completion of last safety visit (270 days)
To evaluate safety and tolerability of CN1 and CN401 in patients with relapsed/refractory lymphoid malignancies through vital signs as assessed by heart rate
Délai: Baseline to End of the Treatment assessed up to an average of 1 year
Measured by vital sign as assessed by heart rate
Baseline to End of the Treatment assessed up to an average of 1 year
To evaluate safety and tolerability of CN1 and CN401 in patients with relapsed/refractory lymphoid malignancies through vital signs as assessed by respiratory rate
Délai: Baseline to End of the Treatment assessed up to an average of 1 year
Measured by vital sign as assessed by respiratory rate
Baseline to End of the Treatment assessed up to an average of 1 year
To evaluate safety and tolerability of CN1 and CN401 in patients with relapsed/refractory lymphoid malignancies through vital signs as assessed by body temperature
Délai: Baseline to End of the Treatment assessed up to an average of 1 year
Measured by vital sign as assessed by body temperature
Baseline to End of the Treatment assessed up to an average of 1 year
To evaluate safety and tolerability of CN1 and CN401 in patients with relapsed/refractory lymphoid malignancies through vital signs as assessed by pulse, systolic blood pressure, and diastolic blood pressure
Délai: Baseline to End of the Treatment assessed up to an average of 1 year
Measured by vital sign as assessed by pulse, systolic blood pressure, and diastolic blood pressure
Baseline to End of the Treatment assessed up to an average of 1 year
To characterize the pharmacokinetics of CN1 and CN401 when administered in combination through Area under the under the drug concentration-time curve.
Délai: Baseline to End of the Treatment assessed up to an average of 1 year
The following parameter is used for evaluation during PK assessments: Area under the drug concentration-time curve (AUC(0-last), AUC0-inf, AUCtau)
Baseline to End of the Treatment assessed up to an average of 1 year
To characterize the pharmacokinetics of CN1 and CN401 when administered in combination through Cmax and Tmax.
Délai: Baseline to End of the Treatment assessed up to an average of 1 year
The following parameter is used for evaluation during PK assessments: Maximum concentration (Cmax) and Time to maximum concentration (Tmax)
Baseline to End of the Treatment assessed up to an average of 1 year
To characterize the pharmacokinetics of CN1 and CN401 when administered in combination through Apparent terminal half-life (t½).
Délai: Baseline to End of the Treatment assessed up to an average of 1 year
The following parameter is used for evaluation during PK assessments: Apparent terminal half-life (t½)
Baseline to End of the Treatment assessed up to an average of 1 year
To characterize the pharmacokinetics of CN1 and CN401 when administered in combination through Apparent terminal elimination rate constant (Kel).
Délai: Baseline to End of the Treatment assessed up to an average of 1 year
The following parameter is used for evaluation during PK assessments: Apparent terminal elimination rate constant (Kel)
Baseline to End of the Treatment assessed up to an average of 1 year
To characterize the pharmacokinetics of CN1 and CN401 when administered in combination through Apparent clearance.
Délai: Baseline to End of the Treatment assessed up to an average of 1 year
The following parameter is used for evaluation during PK assessments: Apparent clearance (CL/F and CL/Fss)
Baseline to End of the Treatment assessed up to an average of 1 year
To characterize the pharmacokinetics of CN1 and CN401 when administered in combination through Accumulation ration.
Délai: Baseline to End of the Treatment assessed up to an average of 1 year
The following parameter is used for evaluation during PK assessments: Accumulation ration (RA)
Baseline to End of the Treatment assessed up to an average of 1 year
To characterize the pharmacokinetics of CN1 and CN401 when administered in combination through Apparent terminal volume of distribution.
Délai: Baseline to End of the Treatment assessed up to an average of 1 year
The following parameter is used for evaluation during PK assessments: Apparent clearance (Vz/F and Vz/Fss)
Baseline to End of the Treatment assessed up to an average of 1 year
To further assess change in anti-tumor activity of CN1 in combination with CN401 through ORR
Délai: Baseline to End of the treatment visit assessed up to an average of 1 year
Measured/determined by Objective Response Rate
Baseline to End of the treatment visit assessed up to an average of 1 year

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

  • Chercheur principal: Jake Shortt, Monash Health

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

28 juillet 2021

Achèvement primaire (Réel)

29 août 2022

Achèvement de l'étude (Réel)

30 septembre 2022

Dates d'inscription aux études

Première soumission

14 avril 2021

Première soumission répondant aux critères de contrôle qualité

6 mai 2021

Première publication (Réel)

10 mai 2021

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

24 octobre 2022

Dernière mise à jour soumise répondant aux critères de contrôle qualité

20 octobre 2022

Dernière vérification

1 octobre 2022

Plus d'information

Termes liés à cette étude

Termes MeSH pertinents supplémentaires

Autres numéros d'identification d'étude

  • CN1-201

Plan pour les données individuelles des participants (IPD)

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Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

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