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Pharmacokinetics, Safety, and Immunogenicity of Bmab1800 and Keytruda® as Adjuvant Monotherapy in Patients With Melanoma

13 mai 2026 mis à jour par: Biocon Biologics UK PLC

A Randomized, Double-blind, Two-arm, Parallel Comparative Multi-center Study to Assess and Compare the Pharmacokinetics, Safety, and Immunogenicity of Bmab1800 and Keytruda® as Adjuvant Monotherapy in Patients With Melanoma

The purpose of the study is to evaluate the pharmacokinetic (PK) equivalence of Bmab1800 as compared with reference product Keytruda® in a randomized, double-blind, two-arm, parallel comparative, multi-center study in patients with resected melanoma (Stage IIB, or Stage IIC, or Stage III) as an adjuvant treatment. This study also compares the safety and immunogenicity of Bmab1800 and Keytruda.

Aperçu de l'étude

Description détaillée

This is a randomized, double-blind, two-arm, parallel-group, multicenter Phase 1 study conducted in adult patients with Stage IIB, IIC, or Stage III melanoma following complete surgical resection. Approximately 138 patients will be randomized in 1:1 ratio to receive either Bmab1800 or Keytruda.

Study treatment will be administered intravenously at a dose of 200 mg every 3 weeks till Week 21. Post which the patient will continue through Week 21, with continuation through Week 24. At Week 24, following completion of all pre dose assessments, patients who were initially randomized to the pembrolizumab arm and who are eligible to continue treatment will transition to the Bmab1800 arm and receive Bmab1800 during an open label treatment period. These patients will continue to receive Bmab1800 through Week 48 (end of treatment for the open label treatment period [EOT OL TP]), with end of study at Week 51 (EOS OL TP), ensuring that all patients receive pembrolizumab equivalent therapy in accordance with recommended treatment guidelines.

The primary objective is to demonstrate PK equivalence based on AUC0-21 and AUC over a dosage interval at steady-state (AUCτ during Cycle 7; Week 18 to Week 21) PK parameters. Safety and immunogenicity will be evaluated through Week 24. Additional safety follow-up during an open-label treatment period through Week 51.

Type d'étude

Interventionnel

Inscription (Estimé)

138

Phase

  • La phase 1

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

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Non

La description

Inclusion Criteria:

  • Male or female patients aged ≥18 years (or legal adult age per local regulations)
  • ECOG Performance Status of 0 or 1 at screening and prior to randomization.
  • Histologically confirmed melanoma that is completely surgically resected with negative margins (per local standard), classified as: Stage IIB, IIC, or Stage III melanoma per AJCC Cancer Staging Manual, 8th edition.
  • Patients must have undergone definitive melanoma resection ≥28 days prior to signing informed consent, and randomization must occur within 12 weeks after surgery.
  • All patients must have disease-free status (ie, no evidence of locoregional recurrence or distant metastasis); no clinical evidence of brain metastases.

Exclusion Criteria:

  • History of ocular/uveal and mucosal melanoma.
  • Active autoimmune disease that has necessitated chronic systemic treatment within 2 years before the first study treatment
  • Active, known, or suspected autoimmune disease that has required systemic treatment in past 2 years.
  • Prior malignancy active within the previous 3 years, except for early-stage cancers (carcinoma in situ or Stage 1) treated with curative intent, basal cell carcinoma of the skin, squamous cell carcinoma of the skin, in situ cervical cancer, in situ prostate cancer, or in situ breast cancer that has undergone potentially curative therapy.
  • Prior therapy with anti-PD-1 (including pembrolizumab), anti PD-L1, anti PD L2, anti CD137, or anti-CTLA-4 antibody (including ipilimumab or any other antibody) or agents that target interleukin-2 (IL-2) pathway any other antibody or drug specifically targeting T cell co-stimulation or checkpoint pathways.
  • Requirement for systemic treatment corticosteroids (>10 mg daily prednisone or equivalent) or other immunosuppressive medications within 14 days of randomization. Inhaled or topical steroids, and adrenal replacement steroid doses > 10 mg daily prednisone or equivalent, are permitted in the absence of active autoimmune disease.
  • History of ocular/uveal and mucosal melanoma.
  • Active autoimmune disease that has necessitated chronic systemic treatment within 2 years before the first study treatment
  • Active, known, or suspected autoimmune disease that has required systemic treatment in past 2 years.
  • Prior malignancy active within the previous 3 years, except for early-stage cancers (carcinoma in situ or Stage 1) treated with curative intent, basal cell carcinoma of the skin, squamous cell carcinoma of the skin, in situ cervical cancer, in situ prostate cancer, or in situ breast cancer that has undergone potentially curative therapy.
  • Prior therapy with anti-PD-1 (including pembrolizumab), anti PD-L1, anti PD L2, anti CD137, or anti-CTLA-4 antibody (including ipilimumab or any other antibody) or agents that target interleukin-2 (IL-2) pathway any other antibody or drug specifically targeting T cell co-stimulation or checkpoint pathways.
  • Requirement for systemic treatment corticosteroids (>10 mg daily prednisone or equivalent) or other immunosuppressive medications within 14 days of randomization. Inhaled or topical steroids, and adrenal replacement steroid doses > 10 mg daily prednisone or equivalent, are permitted in the absence of active autoimmune disease.
  • Receipt of treatment directed against the resected melanoma (eg, chemotherapy, targeted agents, biotherapy, or limb perfusion) administered after the complete resection.
  • History of allergy or hypersensitivity to pembrolizumab or its excipients.
  • History of severe hypersensitivity reaction (Grade ≥3) to any monoclonal antibody.
  • Received prior anticancer therapy including mAb, chemotherapy, or an investigational agent or device within 5 half-lives before first dose of study intervention or not recovered (ie, > Grade 1 or at baseline) from AEs due to previously administered agents at screening and before randomization.
  • Patients with ≤ Grade 2 neuropathy are an exception and may qualify for the study.
  • Received a live vaccine within 30 days prior to the first dose of study intervention.

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: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Double

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Bmab1800
  • 200 mg Q3W, intravenous infusion, over 24 weeks
  • Double-blind period through Week 24; eligible patients may continue in open-label period through Week 48
  • 200 mg Q3W, intravenous infusion, over 24 weeks
  • Double-blind period through Week 24; eligible patients may continue in open-label period through Week 48
Comparateur actif: US-Licensed Keytruda
  • 200 mg Q3W, intravenous infusion, over 24 weeks
  • Double-blind period through Week 24
  • 200 mg Q3W, intravenous infusion, over 24 weeks
  • Double-blind period through Week 24

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Time Curve from Time 0 to 21 Days (AUC₀-₂₁days)
Délai: Week 0 to Week 3
Assessed to compare pharmacokinetics of Bmab1800 and Keytruda®
Week 0 to Week 3
Time Curve Over the Dosing Interval at Steady State (AUCτ)
Délai: Assessed to demonstrate steady-state PK equivalence
Cycle 7 (Week 18 to Week 21)
Assessed to demonstrate steady-state PK equivalence

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Cmax
Délai: From first dose through Week 24 (DB-TP)
From first dose through Week 24 (DB-TP)
tmax
Délai: From first dose through Week 24 (DB-TP)
From first dose through Week 24 (DB-TP)
Cmax,ss
Délai: From first dose through Week 24 (DB-TP)
From first dose through Week 24 (DB-TP)
tmax,ss
Délai: From first dose through Week 24 (DB-TP)
From first dose through Week 24 (DB-TP)
Ctrough
Délai: From first dose through Week 24 (DB-TP)
From first dose through Week 24 (DB-TP)
Incidence and severity of adverse events and serious adverse events
Délai: From first dose through Week 24 (DB-TP)
Assessed by incidence and severity of adverse events and serious adverse events
From first dose through Week 24 (DB-TP)
Immunogenicity
Délai: From first dose through Week 24 (DB-TP)
Assessed by incidence of anti-drug antibodies
From first dose through Week 24 (DB-TP)

Collaborateurs et enquêteurs

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

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 (Estimé)

1 août 2026

Achèvement primaire (Estimé)

15 décembre 2027

Achèvement de l'étude (Estimé)

21 juin 2028

Dates d'inscription aux études

Première soumission

6 mai 2026

Première soumission répondant aux critères de contrôle qualité

6 mai 2026

Première publication (Réel)

12 mai 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

14 mai 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

13 mai 2026

Dernière vérification

1 mai 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

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

Étudie un produit pharmaceutique réglementé par la FDA américaine

Oui

Étudie un produit d'appareil réglementé par la FDA américaine

Non

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