Finding studies
Finding studies
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(Asia sites)Toray Contact for Clinical Trial Information
CONTACT
(US sites) Contact for Clinical Trial Information
CONTACT
Lead
Toray Industries, Inc
This study will assess and compare the efficacy, safety, pharmacokinetics (PK), optimal dose and anti-drug antibodies (ADA) and neutralizing antibodies (NAbs) development of TRK-950 at two separate dose levels in combination with RAM + PTX as compared with RAM + PTX treatment alone in participants with gastric or gastro-esophageal junction (GEJ) adenocarcinoma. The primary objective is progression free survival (PFS). Secondary objectives are overall survival, objective response rate, best overall response, duration of response, disease control rate, safety, pharmacokinetics, and immunogenicity of TRK-950 when used in combination with RAM+PTX.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
