About this trial
Based on overall response rate (ORR) as assessed by the Independent Review Committee (IRC) against the Response Evaluation Criteria in Solid Tumors (RECIST v1.1) criteria for Solid Tumor Efficacy, To evaluate the efficacy of LM-108 in combination with Toripalimab in patients with advanced malignant solid tumours with unresectable or metastatic MSI-H/dMMR who have failed previous anti-PD-1 /PD-L1 therapy.
Eligibility criteria
Qualifiers
Subjects with advanced solid tumors diagnosed by pathology have evidence of advanced stage or metastasis that cannot be surgically removed. And the MSI-H status will be confirmed by central laboratory designated of the sponsor.
Aged 18.
Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.
At least one measurable lesion.
Disqualifiers
Subjects with symptomatic/active central nervous system (CNS) metastases.
Subject who have uncontrollable pleural effusion, pericardial effusion, and ascites despite treatment such as puncture and drainage Within 14 days prior to enrollment; Pericardial effusion accompanied by clinical symptoms or moderate or above.
Subjects' weight decreased by more than 20% within the first 2 months of enrollment.
Poorly controlled tumor-related pain.
Trial design
Treatments tested in this trial
- LM-108
- Toripalimab
Treatment groups
Sponsors and collaborators
LaNova Medicines Limited
Lead sponsor
Chia Tai Tianqing Pharmaceutical Group Co., Ltd.
Collaborator