Gastric Adenocarcinoma
Conditions
Brief summary
The main purpose of this study is to evaluate the efficacy and safety of sintilimab plus ramucirumab compared to stand of care first-line chemotherapy in participants with advanced gastric or esophagogastric adenocarcinoma.
Detailed description
This is a randomized, multicenter, phase 3 study to evaluate the efficacy and safety of sintilimab combined with ramucirumab as compared to stand of care chemotherapy for the first-line treatment of PD-L1 positive, unresectable locally advanced or metastatic gastric or gastroesophageal junction adenocarcinoma. The primary endpoint of this study is OS of the ITT population.
Interventions
DRUGSintilimab
Administered IV
DRUGRamucirumab
Administered IV
DRUGCisplatin
Administered IV
DRUG5-fluorouracil
Administered IV
DRUGOxaliplatin
Administered IV
DRUGCapecitabine
Administered orally
Sponsors
Innovent Biologics (Suzhou) Co. Ltd.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
* Have a histologically confirmed diagnosis of gastric or gastroesophageal junction adenocarcinoma * With HER2 negative and PD-L1 positive tumor tissue * Have fresh or archival tumor tissue samples within 6 months for PD-L1 expression test. * Age ≥18 and ≤75 years * Diagnosed as unresectable locally advanced or metastatic stage
Exclusion criteria
* Have received any prior palliative systemic treatment for advanced gastric or gastroesophageal junction adenocarcinoma. * Known to have central nervous system metastases, cancerous meningitis, or bone metastases with a risk of paraplegia * Known bone metastasis with a risk of paraplegia. * Have any ascites that requires intervention. * With bilateral medium pleural effusion or unilateral large pleural effusion leading to respiratory symptoms
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Safety and tolerability of sintilimab plus ramucirumab,Overall survival (OS) | Randomization to Death from Any Cause, up to 60 months | OS is time from the date of randomization to the date of death from any cause. If the participant is alive at the cutoff for analysis (or was lost to follow-up), OS data is censored for analysis on the last date the participant is known to be alive. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Progression-free Survival (PFS) | Randomization to Radiological Disease Progression or Death from Any Cause (Up to 24 Months) | PFS is time from the date of randomization to the date of radiographic documentation of progression (per RECIST v.1.1) or the date of death due to any cause, whichever is earlier. If a participant is not known to have died or have radiographic documented progression as of the data cutoff date for the analysis, the PFS time is censored at the last adequate tumor assessment date. |
| Objective Response Rate [ORR] (Percentage of Participants With Complete Response [CR] or Partial Response [PR]) | Randomization to Disease Progression (Up To 24 Months) | Response is defined using RECIST v1.1. ORR is calculated as sum of the number of participants with CR and PR divided by the number of evaluable participants multiplied by 100. |
| Disease Control Rate [DCR] (Percentage of Participants With Complete Response [CR], Partial Response [PR] or Stable Disease [SD]) | Randomization to Disease Progression (Up To 24 Months) | Response is defined using RECIST v1.1. DCR is calculated as sum of the number of participants with CR, PR, and SD divided by the number of evaluable participants multiplied by 100. |
| Duration of Response (DoR) | Date of Complete Response (CR) or Partial Response (PR) to Date of Objective Disease Progression or Death Due to Any Cause (Up To 24 Months) | DoR is time from the date of first radiographic documentation of CR or PR to the date of first radiographic documentation of PD or death due to any cause. If a participant is not known to have died or have radiographically documented PD as of the data inclusion cutoff date, DOR is censored at the date of the last adequate tumor assessment. |
| Number of participants experiencing an adverse event (AE) | Randomization to end of study (up to 24 months) | An AE was defined as any untoward medical occurrence in a participant administered a pharmaceutical product and which did not necessarily have a causal relationship with this treatment. The number of participants who experienced an AE is reported for each arm according to the treatment received. |
Countries
China
Outcome results
None listed