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SGLT2 Inhibitors and Survival in Lung Cancer Patients With Diabetes

The Impact of SGLT2i on the Outcome of Advanced Lung Cancer in Patients With Diabetes

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07272057
Enrollment
200
Registered
2025-12-09
Start date
2025-12-07
Completion date
2026-11-07
Last updated
2025-12-09

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

Conditions

Lung Cancer

Brief summary

The goal of this clinical trial The goal of this clinical trial is to evaluate whether SGLT2 inhibitor drugs can extend overall survival or delay the progression of the tumor in patients with both advanced lung cancer and diabetes. It will also check if these drugs are safe for these patients. The main questions it aims to answer are: * Does adding an SGLT2 inhibitor to standard cancer treatment improve survival? * Does it cause more or fewer cardiovascular toxicity? * What side effects do participants experience? Researchers will compare a group taking an SGLT2 inhibitor to a group not taking SGLT2 inhibitor to see if the drug works. Participants will: * Be adults diagnosed with advanced lung cancer and type 2 diabetes. * Take either the SGLT2 inhibitor pill or other hypoglycemic drugs once a day alongside their cancer treatment. * Undergo regular clinical visits for monitoring, laboratory tests, and imaging studies

Interventions

SGLT2 inhibitors used for patients with lung cancer and diabetes

OTHERSham (No Treatment)

SGLT2 inhibitors are not used for patients with lung cancer and diabetes

Sponsors

Shanghai Chest Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Lung cancer patients receiving standard anti-tumor treatment; type 2 diabetes; patients with a score of 0-2 assessed by Eastern Cooperative Oncology Group's performance status; the patients agreed to participate in this study.

Exclusion criteria

* Severe abnormalities in liver, kidney or heart functions; expected lifespan less than 3 months.

Design outcomes

Primary

MeasureTime frame
Number of Participants with deathFrom enrollment to the end of treatment at 12 months

Secondary

MeasureTime frame
Number of Participants with new-onset atrial fibrillation/flutter, acute coronary syndrome, myocarditis, massive pericardial effusion, heart failure and third-degree atrioventricular block.From enrollment to the end of treatment at 12 months

Contacts

Primary ContactJindong Chen
cjdxk2016@163.com+862122200000

Outcome results

None listed

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