Skip to content

Multi-center clinical study of efficacy and safety of Cadonilimab (AK104) combined with albumin-paclitaxel and platinum in first-line treatment of extensive small cell lung cancer (ES-SCLC)

Multi-center clinical study of efficacy and safety of Cadonilimab (AK104) combined with albumin-paclitaxel and platinum in first-line treatment of extensive small cell lung cancer (ES-SCLC)

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300077241
Enrollment
Unknown
Registered
2023-11-02
Start date
2023-11-02
Completion date
Unknown
Last updated
2023-11-06

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

Conditions

Lung cancer

Interventions

Single arm:Cadonilimab (AK104) combined with albumin-paclitaxel and platinum

Sponsors

Zhujiang Hospital of Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Aged 18 to 75 years; (2) Patients with extensive small-cell lung cancer; (3) ECOG PS: 0-1; (4) Good organ function: a) Hematology: WBC =3.0×10^9/L; ANC =1.5×10^9/L; HGB =80 g/L; PLT =100×10^9/L; b) Liver function: TBIL = 1.5 ×ULN; AST, ALT = 2.5 × ULN; c) INR =1.5 ×ULN or PT =1.5 ×ULN or aPTT =1.5 ×ULN; d) Renal function: CREAT < 1.5 ×ULN (5) No prior systemic therapy for SCLC; (6) The estimated survival time is greater than 2 months; (7) Patients volunteer to participate in the study and sign informed consent.

Exclusion criteria

Exclusion criteria: (1) Symptomatic brain metastases; (2) Autoimmune disease; (3) Previous exposure to T cell co-stimulation therapy or immune checkpoint inhibitors; (4) Having active infection; (5) Known allergy to the investigational drug: known severe allergic reaction to monoclonal antibodies of any kind; A history of allergy to paclitaxel-albumin or platinum; (6) Pregnant or lactating women; (7) Other conditions that are not suitable for inclusion according to the researcher.

Design outcomes

Primary

MeasureTime frame
half-year progression-free survival rate;

Secondary

MeasureTime frame
Progression-Free Survival;overall survival ;half-year overall survival rate;one-year overall survival rate;Objective Response Rate;quality of life;adverse effect;

Countries

China

Contacts

Public ContactJian Zhang

Zhujiang Hospital of Southern Medical University

blacktiger@139.com+86 139 2509 1863

Outcome results

None listed

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