drugset / Trial / NCT03202927
Comparative Immunogenicity Study Comparing TPI-120 to Neulasta® in Healthy Adult Subjects
RandomizedParallel-groupSingle-blindTreatment
Summary
This study will compare treatment emergent incidence rate of ADA between TPI-120 and US licensed Neulasta in normal healthy adult subjects
Timeline
- Start
- 2017-03-25
- Primary completion
- 2018-03-01
- Completion
- 2018-04-12
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Pegfilgrastim | Protein / enzyme biologic | 6 mg | Subcutaneous |
Indications
No indication recorded.