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A Multicenter, Real-world Study of Adebrelimab in the Treatment of Extensive Stage Small Cell Lung Cancer

A Multicenter, Real-world Study of Adebrelimab in the Treatment of Extensive Stage

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06267170
Acronym
SCLC
Enrollment
288
Registered
2024-02-20
Start date
2024-02-25
Completion date
2026-02-25
Last updated
2024-02-20

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

Conditions

SCLC,Extensive Stage

Brief summary

This study collected data on patients with extensive stage small cell lung cancer treated with Adebrelimab to investigate its safety and efficacy

Interventions

DRUGAdebrelimab

Treatment with adbelizumab

Sponsors

Henan Cancer Hospital
Lead SponsorOTHER_GOV

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Sign informed consent and join the study voluntarily; 2. Patients diagnosed with extensive small cell lung cancer; 3. Age ≥18 years old; 4. Have at least one measurable lesion (according to RECIST 1.1); 5. The investigators judged that adebrelimab treatment was acceptable; 6. Contraception: Patients should agree that it must be used during the study period and within 6 months after the study ends Effective contraception;

Exclusion criteria

1. Allergic to adebrelimab and its excipients; 2. Patients who have also received other immune drugs or therapies; 3. Patients who are participating in other interventional studies; 4. patients with other malignant tumors; 5. Pregnant or lactating women; 6. The investigator considers that the patient is not suitable to participate in any other conditions of the study.

Design outcomes

Primary

MeasureTime frameDescription
Safety (Occurrence of ≥ Grade 3 AE)End of each cycle (each cycle is 28 days)The incidence of grade 3 or higher adverse events

Secondary

MeasureTime frameDescription
PFSEnd of every two cycles (each cycle is 28 days)Progression free survival
ORREnd of every two cycles (each cycle is 28 days)Objective response rate
OSEnd of every two cycles (each cycle is 28 days)Overall survival
DCREnd of every two cycles (each cycle is 28 days)Disease control rate

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026