M108 Plus CAPOX Versus Placebo Plus CAPOX as First-line Treatment for Claudin (CLDN) 18.2-Positiv… (NCT06177041) | Clinical Trial Compass
RecruitingPhase 3
M108 Plus CAPOX Versus Placebo Plus CAPOX as First-line Treatment for Claudin (CLDN) 18.2-Positive, HER2-Negative, PD-L1 CPS<5, Locally Advanced Unresectable or Metastatic Gastric or Gastroesophageal Junction (GEJ) Adenocarcinoma.
China486 participantsStarted 2023-12-25
Plain-language summary
Gastric/GEJ adenocarcinoma, which is one of the major leading causes of cancer-related deaths worldwide, is a global challenge to human health. However, standard chemotherapy has limited efficacy in advanced gastric cancer, and there is an urgent need to explore and develop new therapeutic targets and combination therapy modalities. The main purpose of this study is to explore the efficacy of M108 monoclonal antibody plus capecitabine and oxaliplatin (CAPOX) versus placebo plus CAPOX as first-line treatment measured by progression free survival (PFS). This study will also evaluate safety, tolerability, pharmacokinetics and the immunogenicity profile of M108 monoclonal antibody, as well as its effects on quality of life.
Who can participate
Age range18 Years – 75 Years
SexALL
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Inclusion criteria
✓. Written informed consent
✓. Histologically confirmed diagnosis of locally advanced unresectable or metastatic gastric/GEJ adenocarcinoma with no treatment previously. For patients with neoadjuvant/adjuant chemotherapy in the past, duration of last therapy to recurrence should be more than 6 months
✓. At least 1 measurable site of the disease according to RECIST 1.1 criteria.
✓. Positive CDLN 18.2 expression
✓. Negative HER2 expression, PD-L1 CPS\<5
✓. ECOG performance status (PS) 0-1
✓. Life expectancy \> 3 months
✓. Age ≥ 18 years and ≤75 years
Exclusion criteria
✕. Previous radiotherapy within 4 weeks prior to the start of study treatment. (if palliative radiotherapy was given to bone metastases and the patient recovered from acute toxicity was allowed).
What they're measuring
1
Progression free survival (PFS)
Timeframe: From date of randomization to the date of disease progression, death or end of study, assessed up to 24 months
. Previous anti-tumor therapy within 4 weeks prior to the start of study treatment.
✕. Previous major operation within 4 weeks prior to the start of study treatment.
✕. Have a prior severe allergic reaction or intolerance to known components of M108 monoclonal antibodies or other monoclonal antibodies (including humanized or chimeric antibodies); Allergic or intolerant to any component of capecitabine, oxaliplatin, etc.
✕. Subject who has been treated with CLDN18.2 monoclonal/bispecific antibodies, CLDN18.2 CAR-T, CLDN18.2 ADC and any therapies that target CLDN18.2.
✕. Subject who is in pregnant or in lactation period.
✕. Other clinically significant disease which may have adversely affected the safe delivery of treatment within this study.