drugset / Trial / NCT03292484
Longer-term Study of AR101 in Subjects Who Participated in a Prior AR101 Study (ARC008)
NaSingle-groupOpen-labelTreatment
Summary
The purpose of this study is to assess AR101's safety, tolerability and efficacy over an extended dosing period.
Timeline
- Start
- 2017-11-02
- Primary completion
- 2023-04-27
- Completion
- 2023-04-27
Publications
- Nilsson C, Scurlock AM, Dellon ES, Brostoff JM, Pham T, Ryan R, Brown KR, Adelman DC, Aceves SS. Onset of eosinophilic esophagitis during a clinical trial program of oral immunotherapy for peanut allergy. J Allergy Clin Immunol Pract. 2021 Dec;9(12):4496-4501. doi: 10.1016/j.jaip.2021.07.048. Epub 2021 Aug 11. No abstract available.
- Fernandez-Rivas M, Vereda A, Vickery BP, Sharma V, Nilsson C, Muraro A, Hourihane JO, DunnGalvin A, du Toit G, Blumchen K, Beyer K, Smith A, Ryan R, Adelman DC, Jones SM. Open-label follow-on study evaluating the efficacy, safety, and quality of life with extended daily oral immunotherapy in children with peanut allergy. Allergy. 2022 Mar;77(3):991-1003. doi: 10.1111/all.15027. Epub 2021 Sep 24.
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | AR101 | Protein / enzyme biologic | 300 mg | Oral |