drugset / Trial / NCT00960115
Study of Tecemotide (L-BLP25) in Participants With Stage III Unresectable Non-small Cell Lung Cancer (NSCLC) Following Primary Chemoradiotherapy
Phase 1/2
Completed
178 enrolled
Merck KGaA, Darmstadt, Germany
Merck Serono Co., Ltd., Japan · collab
RandomizedParallel-groupDouble-blindTreatment
Summary
This is a phase I/II study in Japan to evaluate the safety of EMD531444 and its effects on survival time in patients with stage III unresectable non-small cell lung cancer.
Timeline
- Start
- 2008-12
- Primary completion
- 2014-05
- Completion
- 2015-06
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Tecemotide | Vaccine | 930 ug | Subcutaneous |
| Background | Cyclophosphamide | Other / unclassified | 300 mg/m2 | Intravenous |