drugset / Trial / NCT01571895
Pilot Efficacy and Safety Study of Oral DF2156A in Patients With Active Bullous Pemphigoid
NaSingle-groupOpen-labelTreatment
Summary
The objective of this clinical trial was to evaluate whether DF2156A has a potential in improving the clinical outcome in patients with active blistering bullous pemphigoid (BP) to warrant its further development. The safety of DF2156A in the specific clinical setting was also evaluated.
Timeline
- Start
- 2012-02-20
- Primary completion
- 2012-07-05
- Completion
- 2012-07-05
Outcome
Outcome not reported
Stopped (Enrollment): “Lack of efficacy observed at 1/3 of the enrollment at investigated dosage. No results available.”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | DF2156A | Small molecule | 150 mg | Oral |