SY001 Targets Mesothelin in a Single-arm, Dose-increasing Setting in Subjects With Advanced Solid Tumors

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-75
SponsorCell Origin Biotech (Hangzhou) Co., Ltd.

About this trial

Single-arm, dose-increasing setting study of CAR macrophages in Mesothelin overexpressing solid tumors.

Eligibility criteria

Qualifiers

Patients with pathologically diagnosed advanced ovarian cancer/pancreatic cancer who have failed at least 1 prior lines treatment, and tumor tissue samples were positive for mesothlin IHC staining;

According to the RECIST 1.1, there is measurable tumor lesions (non-lymph node lesion 10mm in length or lymph node lesion 15mm in diameter measured by CT or MRI, with scan layer thickness 5mm);

Eastern Cooperative Oncology Group (ECOG) score of 2 and satisfactory major organ functions;

Estimated life expectancy >3 months;

Disqualifiers

Pregnant or lactating women;

Any uncontrollable active infection, including but not limited to active tuberculosis, HBV infection;

Patients who have a history of other mesothelin-targeting therapy;

Patients who have a history of autoimmune disease;

Trial design

Treatments tested in this trial

  • SY001

Treatment groups

2 Participants
are divided into 1 treatment group