Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05068232

Durvalumab and Ablative Radiation in Small Cell Lung Cancer (DARES)

A Phase II Trial of Durvalumab and Ablative Radiation in Extensive-Stage Small Cell Lung Cancer (DARES)

Status
Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
49 (estimated)
Sponsor
University of Chicago · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This this study is for individuals who have treatment-naïve extensive-stage small cell lung cancer (small cell lung cancer that wont respond to treatment). Doctors leading this study hope to learn if combining durvalumab, carboplatin and etoposide with hyofractionated ablative radiation therapy (radiation focused on certain parts of the body) will help treat your cancer and improve how long you can live with extensive-stage small cell cancer without it getting worse (progression-free survival). Your participation in this research will last about 48 months. Durvalumab along with chemotherapy has been approved by the Food and Drug Administration (FDA) for the treatment of small cell lung cancer along with chemotherapy. This study is testing the addition of radiation to durvalumab and chemotherapy.

Conditions

Interventions

TypeNameDescription
RADIATIONAblative RadiationAblative radiation therapy is a highly focused radiation treatment that gives an intense dose of radiation concentrated on a tumor or very specific area of the body, while limiting the radiation that affects surrounding organs.
DRUGDurvalumabDurvalumab is an immunotherapy drug -- a drug used to help boost your immune response to fight cancer.
DRUGEtoposideEtoposide is a chemotherapy drug approved for different kinds of cancer, including small cell lung cancer.
DRUGCarboplatinCarboplatin is a chemotherapy drug approved for different kinds of cancer, including small cell lung cancer.

Timeline

Start date
2022-08-19
Primary completion
2027-10-01
Completion
2027-10-01
First posted
2021-10-05
Last updated
2026-03-04

Locations

2 sites across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT05068232. Inclusion in this directory is not an endorsement.