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Study identifier: NCT05578326 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Study of Trilaciclib and Lurbinectidin

Condition: Lung Cancer · Small-cell Lung Cancer  ·  Sponsor: UNC Lineberger Comprehensive Cancer Center

PhasePhase 2
Planned participants30
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Lung cancer is by far the leading cause of cancer death among both men and women worldwide and the second most common cancer in terms of new cases. Small cell lung cancer (SCLC) is the deadliest form of lung cancer. The standard first-line treatment is the combination of carboplatin, etoposide, and atezolizumab. While response rates for this regimen are high (roughly 60%), the duration of response is short, typically 4 months. Following progression after the 1st line treatment of SCLC, there is no consensus regarding subsequent therapy. Lurbinectedin is FDA approved and is increasingly preferred in clinical practice. Toxicity was significant, but appeared favorable compared to historic results with topotecan, leading to the adoption of this therapy for second-line SCLC. The toxicity profile was dominated by myelosuppression. This study investigates the effect of Trilaciclib on myelosuppression rate in subjects with platinum refractory extensive stage (ES)- SCLC receiving Lurbinectedin as well as the clinical synergy of Trilaciclib and Lurbinectedin combination.

This description comes directly from the study's public registry record.

Talk to the study team

Shamina Williams  ·  919-966-4432  ·  shamina_williams@med.unc.edu

Lauren Higgins  ·  919-966-4432  ·  Lauren_Higgins@med.unc.edu

Always discuss trial participation with your own doctor first.

Locations (2)

Dartmouth Hitchcock Medical CenterLebanon, New Hampshire, United StatesWithdrawn
Lineberger Comprehensive Cancer Center at University of North Carolina Chapel HillChapel Hill, North Carolina, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05578326