drugset / Trial / NCT02865122
Safety and Efficacy Study in Infant With SBS
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The objective of this clinical study is to evaluate the efficacy and safety of NTRA-9620 compared with placebo in pediatric subjects (aged 28 weeks postmenstrual age to 52 weeks old) with SBS following surgical resection
Timeline
- Start
- 2017-03-20
- Primary completion
- 2018-03-22
- Completion
- 2018-03-22
Outcome
Outcome not reported
Stopped (Enrollment): “Sponsor decision based on enrollment”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | NTRA-9620 | Unknown | — | Oral |