Approval Probability
TA Base Rate
Adjusted LOA
ML Risk
Durvalumab · 1 trial · 3 indications
12-month progression free survival was determined for each subject as a binary variable indicating whether or not the subject was progression free and surviving at 12 months after study enrollment. Failure occurred if the subject progressed or died from any cause within 12 months of study enrollment. Disease progression was determined according to RECIST v1.1.
| Arm | Type | Description |
|---|---|---|
| Single Arm | EXPERIMENTAL | SBRT + Concurrent Mediastinal Chemoradiation +/- Consolidation Chemotherapy/Adjuvant Immunotherapy |
| Name | Type | Description |
|---|---|---|
| SBRT | RADIATION | Primary tumor SBRT |
| Carboplatin | DRUG | concurrent chemotherapy |
| Paclitaxel | DRUG | concurrent chemotherapy |
| cis Platinum | DRUG | concurrent chemotherapy |
| Etoposide | DRUG | concurrent chemotherapy |
| IMRT | RADIATION | mediastinal radiation |
| Durvalumab | DRUG | adjuvant immunotherapy |
Inclusion Criteria Subjects must meet all the following criteria: * Histologic or cytologic documentation of NSCLC (all histologies allowed) * Stage II or III disease (AJCC 7th Edition) based on imaging as required during screening: Stage II disease includes only subjects with medically inoperable...
Durvalumab is being studied for use in Lung Cancer Stage II, as well as Lung Cancer Stage III and Non Small Cell Lung Cancer. It is an investigational oncology therapy currently in Phase 2 clinical development, evaluated in a trial that combines high dose radiation followed by chemotherapy and radiation.
Durvalumab is a small molecule therapy developed by Atrium Therapeutics, Inc. for oncology indications. Its specific molecular target has not been disclosed in the available clinical trial information. The drug is being investigated for its potential role in treating lung cancers, including Stage II and Stage III disease.
Durvalumab is being developed by Atrium Therapeutics, Inc., a biopharmaceutical company. The company's stock ticker is RNA. Atrium Therapeutics is conducting clinical research on Durvalumab for the treatment of lung cancer, with the drug currently in Phase 2 development.
Durvalumab is currently in Phase 2 clinical development. It is an investigational drug, not yet approved by regulatory authorities. The ongoing Phase 2 trial is active but not recruiting participants, and is designed to evaluate the therapy in patients with lung cancer.
Durvalumab is being evaluated in one clinical trial, identified as NCT03141359. This Phase 2 study, titled 'Use of High Dose Radiation Followed by Chemotherapy and Radiation to Treat Locally Advanced NSCLC,' is active but not recruiting. The trial enrolls 61 participants in the United States and includes patients with Lung Cancer Stage II, Stage III, and Non Small Cell Lung Cancer.
Durvalumab is the drug name used in the clinical trial records for this investigational therapy. No alternative names have been listed in the available information. The drug is being developed by Atrium Therapeutics, Inc. and is currently in Phase 2 testing for lung cancer indications.