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NCT07235280 · ClinicalTrials.gov registry record · Early Phase 1

Testing the Safety of Dapagliflozin Prior to Surgery for the Treatment of Patients With Stage IA Lung Adenocarcinoma

A Early Phase 1 study of Lung Cancer and Lung Adenocarcinoma, sponsored by Jonsson Comprehensive Cancer Center.

Recruiting
Registry status
Early Phase 1
Development phase
48
Enrollment target
1
Study location

NCT07235280: Recruiting Early Phase 1 study of Lung Cancer and Lung Adenocarcinoma, sponsored by Jonsson Comprehensive Cancer Center.

NCT07235280 is a Early Phase 1 study of Lung Cancer and Lung Adenocarcinoma that is actively recruiting participants, run by Jonsson Comprehensive Cancer Center. The registered enrollment target is 48 participants, below the 936-participant average among 409 other Lung Cancer trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07235280, a Early Phase 1 study of Lung Cancer and Lung Adenocarcinoma, is actively recruiting participants, sponsored by Jonsson Comprehensive Cancer Center.

RECRUITING
Registry status
Early Phase 1
Development phase
48 participants
Enrollment target
1
Study location

Study Summary

This early phase I trial tests the safety and side effects of dapagliflozin given prior to surgery in patients with stage IA lung adenocarcinoma. Dapagliflozin is approved by the Food and Drug Administration (FDA) for the treatment of diabetes and heart failure. It is an SGLT2 inhibitor. Stage I lung adenocarcinomas express significantly higher levels of the SGLT2 protein than other stages, and research suggests that SGLT2 inhibition improves lung cancer outcomes in patients with diabetes. In this study, dapagliflozin is being used off-label, which means it is being used for a condition that it was not originally approved for by the FDA. The investigational study drug is a neoadjuvant treatment, meaning the drug is given before surgery to try and help make the surgery more effective.

Primary Outcome

Will be measured by frequency and severity of toxicities related to dapagliflozin per Common Terminology Criteria for Adverse Events version 6.0. Data will be summarized. Adverse events, severe adverse events, and adverse drug reactions will be coded by body system and Medical Dictionary for Regulatory Activities classification term. Adverse events will be tabulated and will include the number of patients for whom the event occurred, the rate of occurrence, and the severity and relationship to s

Interventions

  • PROCEDURE Biospecimen Collection
  • OTHER Questionnaire Administration
  • PROCEDURE Computed Tomography Assisted Biopsy
  • DRUG Dapagliflozin Propanediol

Study Locations (1)

California

  • UCLA / Jonsson Comprehensive Cancer Center - Los Angeles

Trial Details

FieldValue
Enrollment Target 48 participants
Start Date 2025-12-02
Est. Completion 2029-06-29
Phase Early Phase 1
Jonsson Comprehensive Cancer Center

321 total trials

What NCT07235280 shows while recruiting

NCT07235280 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 48 participants, a relatively small participant target, below the 936-participant average among 409 other Lung Cancer trials with a reported enrollment target (95% lower).

The record links to 5 conditions, with Lung Cancer appearing as the primary indexed condition, and to 4 interventions - of which Biospecimen Collection is the first listed.

NCT07235280 reports a single indexed study location in California.

Frequently Asked Questions

What is clinical trial NCT07235280 about?

NCT07235280 is a clinical study titled "Testing the Safety of Dapagliflozin Prior to Surgery for the Treatment of Patients With Stage IA Lung Adenocarcinoma". This early phase I trial tests the safety and side effects of dapagliflozin given prior to surgery in patients with stage IA lung adenocarcinoma. Dapagliflozin is approved by the Food and Drug Administration (FDA) for the treatment of diabetes and heart failure. It is an SGLT2 inhibitor. Stage I lun...

What is the current status of trial NCT07235280?

This trial is currently recruiting. It is a Early Phase 1 study. The enrollment target is 48 participants. The study started on 2025-12-02. Estimated completion is 2029-06-29.

What conditions does trial NCT07235280 study?

This clinical trial studies the following conditions: Lung Cancer, Lung Adenocarcinoma, Stage IA2 Lung Cancer AJCC v8, Stage IA3 Lung Cancer AJCC v8, Stage IA1 Lung Cancer American Joint Committee on Cancer (AJCC) v8.

What interventions are being tested in trial NCT07235280?

The interventions under investigation include: Biospecimen Collection (PROCEDURE), Questionnaire Administration (OTHER), Computed Tomography Assisted Biopsy (PROCEDURE), Dapagliflozin Propanediol (DRUG).

Who is sponsoring clinical trial NCT07235280?

This trial is sponsored by Jonsson Comprehensive Cancer Center, which has 321 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07235280 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Lung Cancer

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT07235280's enrollment target sits among peer trials

48 272nd of 409 higher than 136 of 409 other Lung Cancer trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Lung Cancer trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT07235280, the US trial registry maintained by the National Library of Medicine. NCT07235280 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.