A Trial to Evaluate the Efficacy, Safety and Tolerability of Subcutaneous TRV250
Stopped Because there have been significant enrollment struggles which has been exacerbated by the COVID impact. This has caused an undue delay to the study timelines and its enrollment goals beyond the business needs.
Conditions
Interventions
- DRUG: Part A: TRV250-20mg/ml
- DRUG: Placebo
- DRUG: Part B: TRV250 Dose 1
- DRUG: Part B: TRV250 Dose 2
- DRUG: Part B: TRV250 Dose 3
- DRUG: Placebo
Sponsor
Trevena Inc.