A Phase II study of Concurrent Chemoradiation plus Durvalumab (MEDI4736) followed by Surgery followed by Adjuvant Durvalumab (MEDI4736) in medically operable patients with surgically resectable Stage III (N2) Non-Small Cell Lung Cancer
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- STATUS
- Recruiting
Summary
The purpose of this study is to estimate the pathological complete response rate at the time of surgery in patients with stage IIIA (N2) NSCLC treated with concurrent Carboplatin/Paclitaxel/Durvalumab plus radiation therapy followed by surgical resection followed by adjuvant Durvalumab.
Description
We are doing this study to find out if the combination of chemotherapy, radiation and FDA approved Durvalumab, followed by surgical resection of your cancer is safe and if it will keep your disease away for a longer period of time. We are also looking at whether adding Durvalumab maintenance after surgical reseaction will provide a longer period of time that your cancer is inactive.
Details
| Condition | Non-Small Cell Lung Cancer |
|---|---|
| Age | 18years - 100years |
| Clinical Study Identifier | TX10373 |
| Last Modified on | 19 February 2024 |
Eligibility
How to participate?
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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