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Construction of Clinical Application Solutions for Multi-modal Tumor Treatment

Construction of Clinical Application Solutions for Multi-modal Tumor Treatment

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400085387
Enrollment
Unknown
Registered
2024-06-06
Start date
2024-06-17
Completion date
Unknown
Last updated
2024-07-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Advanced solid tumor

Interventions

multi-modal +PD1:Treatment with anti-PD-L1 monoclonal antibody system was initiated on day 7 after ablation
multi-modal +SGN1:Ablation d1, d8 and d15 were administered intratumoral with SGN1

Sponsors

Shanghai Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: ? Age 18-75 years old, gender is not limited; ? Advanced solid tumors with definite pathological or clinical diagnosis, primary tumors and metastases that cannot be resected or cannot tolerate or refuse to be resected; (3) If the primary lesion can not be resected or recurred, there are no serious complications such as bleeding and obstruction; ? First-line treatment failed; For those who have previously received chemotherapy, radiotherapy or local liver treatment, the interval between the last systemic treatment or local liver treatment is at least 1 month; ?Child-Pugh A or B; Bilirubin =3.0 mg/dL, creatinine =2.5 mg/dL, white blood cell count = 2.0 ×10^9/L, platelet = 100×10^9/L; ?ECOG PS =2.

Exclusion criteria

Exclusion criteria: ?Liver function Child-Pugh grade C; ? Expected survival < 3 months; ? Insufficiency or failure of important organs; ? There is active infection; (5) Uncorrectable coagulation abnormalities; ? Refractory ascites, pleural fluid or bad fluid; ? can not cooperate with the treatment; (8)The researchers determined that there were any other factors that were not suitable for inclusion or affected participants' participation in the study.

Design outcomes

Primary

MeasureTime frame
3 months mPFSR;

Secondary

MeasureTime frame
ORR;PFS;CBR;DOR;

Countries

China

Contacts

Public ContactHaiyan Hu

Shanghai Sixth People's Hospital

xuri1104@163.com+86 189 3017 4575

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026