A Study of KN026-based Combination Therapy in HER2-positive Gastric Cancer

Trial statusNot yet recruiting
Trial phasePhase 2, Phase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorShanghai JMT-Bio Inc.

About this trial

This study is designed to compare the efficacy and safety of KN026 combined chemotherapy with or without Enlonstobart versus Trastuzumab combined chemotherapy with or without Pembrolizumab as first-line treatment in HER2-positive unresectable locally advanced or metastatic gastric cancer.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Histologically or cytologically confirmed diagnosis of gastric cancer.

Participants unresectable locally advanced or metastatic gastric cancer who had not received systemic treatment (participants who had progressed 6 months after prior neoadjuvant/adjuvant therapy could be enrolled).

Confirmed to be HER2 positive (HER2-positive is defined as IHC 3+ or IHC 2+ with ISH positive) and PD-L1 status (participants of phase III should be confirmed by the pathology department of participating study center).

Phase II: Presence of at least 1 measurable lesion per RECIST 1.1. Tumor lesions situated in a previously irradiated area are considered measurable if progression has been demonstrated in such lesions. Phase III:Presence of at least 1 evaluable lesion per RECIST 1.1. Tumor lesions situated in a previously irradiated area are considered measurable if progression has been demonstrated in such lesions.

Disqualifiers

Has received anti-tumor treatment such as systemic chemotherapy or other trial interventions within 28 days, or immunotherapy (e.g. interleukin, interferon, thymospipeptide, etc.), hormone therapy or targeted therapy within 14 days or 5 half-life (whichever is shorter) before randomization.

Participants with brain metastasis or spinal cord compression at screening (except for completed local treatment and discontinued glucocorticoids for at least 4 weeks before randomization , and stable central nervous system imaging and brain metastasis symptoms for at least 4 weeks).

Participants with PD-L1 CPS ≥1, who are receiving long-term immunotherapy (e.g., cyclosporine) or require daily systemic steroid therapy (e.g., >20 mg prednisone or equivalent), except those who treated with local glucocorticoids using nasal spray, inhalation, or other pathways.

Participants with PD-L1CPS ≥1, who have an active autoimmune disease or have a history of autoimmune disease 2 years before randomization and still require systemic treatment. However, participant with the following diseases is allowed to enroll: well-controlled type I diabetes, well-controlled hypothyroidism that requires hormone replacement therapy, skin diseases that do not require systemic treatment (such as vitiligo, psoriasis, or hair loss), or participant who is expected to not recur without external triggers.

Trial design

Design model

Parallel

Treatments tested in this trial

  • KN026

    Drug

    In accordance with the protocol

  • Capecitabine

    Drug

    Capecitabine is for oral administration.

  • Enlonstobart

    Drug

    Enlonstobart is administered by intravenous infusion.

  • Oxaliplatin

    Drug

    Oxaliplatin is administered by intravenous infusion.

  • Trastuzumab

    Drug

    Trastuzumab is administered by intravenous infusion.

  • Pembolizumab

    Drug

    Pembolizumab is administered by intravenous infusion.

  • Cisplatin

    Drug

    Cisplatin is administered by intravenous infusion.

  • Fluorouracil

    Drug

    Fluorouracil is administered by intravenous infusion.

Treatment groups

490 Participants
are divided into 4 treatment groups
Group A: Group A:Combination of KN026 and CAPOX/PF with or without enlonstobartExperimental treatment 6 interventions
Group B: Group B: Combination of trastuzumab, and CAPOX/PF with or without enlonstobartExperimental treatment 6 interventions
Group C: Experimental group: Combination of KN026 and CAPOX/PF with or without enlonstobartExperimental treatment 6 interventions
Group D: Control group:Combination of trastuzumab and CAPOX/PF with or without PembrolizumabExperimental treatment 6 interventions

Trial outcomes

Primary outcomes

1

Objective Response Rate (ORR) by investigator in Phase II

Time frame
Up to approximately 5 years
2

Progression-Free Survival (PFS) by BIRC in Phase III

Time frame
Up to approximately 5 years

Secondary outcomes

1

Overall Survival (OS) in Phase III

Time frame
Up to approximately 5 years

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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