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NCT06562647Recruiting

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

An Exploratory Clinical Trial to Evaluate the Safety, Tolerability, Pharmacokinetics, and Initial Efficacy of SY001 Injection Targets Mesothelin in a Single-arm, Dose-increasing Setting in Subjects With Advanced Solid Tumors

Source: ClinicalTrials.gov · Last updated 13 Feb 2026

Brief summary (registry, in English)

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

Status (registry)
Recruiting
Study type
Interventional
Enrollment
2 (estimated)
First submitted
15 Aug 2024
Start date
12 Apr 2023
Primary completion date
Dec 2026
Lead sponsor
Cell Origin Biotech (Hangzhou) Co., Ltd.
NCT number
NCT06562647

What you commit to

  • Study type: Interventional
  • Planned participants: 2
  • From 12 Apr 2023 to the primary completion date, Dec 2026
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • 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;

Other

  • Pregnant or lactating women;
  • The investigator assessed that the patient was unable or unwilling to comply with the requirements of the study protocol.

Who the study is looking for

  • 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;
  • Female patients of childbearing age must undergo a serum pregnancy test at screening and prior to pretreatment and the results must be negative, and are willing to use a very effective and reliable method of contraception within 1 year after the last study treatment.

Age in the registry: 18 years to 75 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The First Affiliated Hospital Zhejiang University School of Medicine
Coordinator of this site? Confirm its status
HangzhouChinaRecruiting
LinYi Cancer Hospital
Coordinator of this site? Confirm its status
LinyiChinaNot yet recruiting

This page is information, not medical advice. Discuss any trial with your doctor.