Approval Probability
TA Base Rate
Adjusted LOA
ML Risk
Durvalumab · 1 trial · 2 indications
Adverse events (AEs) were coded using the Medical Dictionary for Regulatory Activities (MedDRA) Version 20.0 and classified by MedDRA system organ class (SOC) and preferred term. The severity was assessed according to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version 4.03. AEs were reported based on clinical laboratory tests, vital signs, physical examinations, and any other medically indicated assessments, including subject interviews, from the time informed consent was signed through 90 days after the last dose of study treatment. TEAEs are AEs that occurred or worsened in severity after administration of the first dose of study treatment. For each arm, the first 6 subjects were evaluated for dose limiting toxicities (DLTs). Deaths within the AE Reporting Period included all deaths that occurred during the study treatment period, or up to 90 days after the administration of the last dose of study drug or initiation of a new treatment.
| Arm | Type | Description |
|---|---|---|
| Arm A: BI 1361849 mRNA Vaccine + durvalumab | EXPERIMENTAL | The BI 1361849 mRNA vaccine comprises 6 drug product components (F2408 coding for MUC1, F2409 coding for survivin, F2410 coding for NY-ESO-1, F2624 coding for 5T4, F2625 coding for MAGE-C2, and F2626 coding for MAGE-C1), which were provided and administered separately; each component was administered twice, thus there were 12 intradermal administrations of 100 µL (80 µg) each for each dose. The PharmaJet Tropis® device was used for the administration of the BI 1361849 components. Durvalumab 1500 mg was to be administered as an intravenous (IV) infusion every 4 weeks for 12 cycles; BI 1361849 was to be administered as 14 doses over the 12 cycles. |
| Arm B: BI 1361849 mRNA Vaccine + durvalumab + tremelimumab | EXPERIMENTAL | The BI 1361849 mRNA vaccine comprises 6 drug product components (F2408 coding for MUC1, F2409 coding for survivin, F2410 coding for NY-ESO-1, F2624 coding for 5T4, F2625 coding for MAGE-C2, and F2626 coding for MAGE-C1), which were provided and administered separately; each component was administered twice, thus there were 12 intradermal administrations of 100 µL (80 µg) each for each dose. The PharmaJet Tropis® device was used for the administration of the BI 1361849 components. Durvalumab 1500 mg was to be administered as an intravenous (IV) infusion every 4 weeks for 12 cycles; tremelimumab 75 mg was to be administered as an intravenous (IV) infusion every 4 weeks for the first 4 cycles (Arm B only); BI 1361849 was to be administered as 14 doses over the 12 cycles. |
| Name | Type | Description |
|---|---|---|
| Durvalumab | DRUG | anti-PD-L1 |
| Tremelimumab | DRUG | anti-CTLA-4 |
| BI 1361849 | BIOLOGICAL | mRNA Vaccine |
| PharmaJet Tropis® device | DEVICE | The PharmaJet Tropis® device was used for the intradermal administration of the BI 1361849 vaccine components. |
Inclusion Criteria 1. Histologic confirmation of metastatic NSCLC. For subjects with known EGFR or ALK/ROS-1 mutations, prior therapy must have included an EGFR tyrosine kinase inhibitor or ALK/ROS-1 inhibitor, respectively. Subjects may have had 1 prior line of anti-PD-1/PD-L1 therapy. Subjects wh...
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Durvalumab is being studied for use in Metastatic Non-small Cell Lung Cancer (NSCLC). It is an investigational therapy in clinical development, and it has not been approved for this indication. The drug is being evaluated in a completed Phase 1 clinical trial to assess its safety and efficacy in patients with this condition.
Durvalumab is being developed by CureVac N.V., a biopharmaceutical company traded on the NASDAQ under the ticker symbol CVAC. The company is conducting clinical research on this drug for the treatment of Metastatic Non-small Cell Lung Cancer.
Durvalumab is in Phase 1 of clinical development. It is an investigational drug being studied for Metastatic Non-small Cell Lung Cancer. The Phase 1 trial has been completed, and the drug remains in clinical development as it has not yet received regulatory approval.
Durvalumab was studied in a completed Phase 1 clinical trial with the identifier NCT03164772. This trial was titled 'Phase 1/2 Study of Combination Immunotherapy and Messenger Ribonucleic Acid (mRNA) Vaccine in Subjects With NSCLC' and enrolled 61 participants in the United States.
Durvalumab is not FDA approved. It is an investigational drug currently in clinical development for Metastatic Non-small Cell Lung Cancer. The drug has completed a Phase 1 trial, but it has not received approval from the FDA or any other regulatory authority.