Literature DB >> 25073663

Single-use autoinjector for peginterferon-β1a treatment of relapsing-remitting multiple sclerosis: safety, tolerability and patient evaluation data from the Phase IIIb ATTAIN study.

Ali Seddighzadeh1, Serena Hung, Krzysztof Selmaj, Yue Cui, Shifang Liu, Bjoern Sperling, Peter A Calabresi.   

Abstract

OBJECTIVES: A sub-study to evaluate safety, tolerability, ease-of-use and patient satisfaction with a single-use autoinjector administering subcutaneous peginterferon-β1a (a pegylated interferon-β1a in clinical development) in a subset of relapsing-remitting multiple sclerosis (MS) patients participating in ATTAIN, a long-term dose-frequency blinded extension of the Phase III randomized ADVANCE study.
METHODS: Over 8 weeks, patients self-administered peginterferon-β1a 125 µg or placebo every 2 weeks (two injections via manual pre-filled syringe [PFS]; two injections via single-use autoinjector). Primary end points were incidence of adverse events (AEs), patient assessment of injection pain score (10-point Visual Analog Scale), and clinician assessment of injection site reactions (ISRs). Secondary objectives included patient assessment of ease-of-use and satisfaction with the autoinjector and evaluation of autoinjector training materials.
RESULTS: In 39 patients, the safety profile of peginterferon-β1a was similar when delivered via autoinjector or PFS; AEs were mostly mild or moderate in severity. Clinicians and patients reported a similar tolerability profile using both PFS and autoinjector, and pain scores were low (< 1), with no reports of clinician-assessed ISRs after administration with the autoinjector. Patients perceived the single-use autoinjector to be easy to use and convenient; overall patient satisfaction with the autoinjector and accompanying training materials was high.
CONCLUSION: The safety and tolerability profile of peginterferon-β1a delivered via autoinjector was similar to delivery via PFS. Patients found the autoinjector easy to use and convenient; this device may simplify the injection process for MS patients who require long-term therapy, thereby potentially improving patient's quality of life and adherence.

Entities:  

Keywords:  IFN-β1a; dosing frequency; drug delivery system; multiple sclerosis; patient outcomes assessments; peginterferon; pegylation

Mesh:

Substances:

Year:  2014        PMID: 25073663     DOI: 10.1517/17425247.2014.944159

Source DB:  PubMed          Journal:  Expert Opin Drug Deliv        ISSN: 1742-5247            Impact factor:   6.648


  6 in total

1.  Usability of a new disposable autoinjector platform device: results of a formative study conducted with a broad user population.

Authors:  Jakob Lange; Philipp Richard; Nick Bradley
Journal:  Med Devices (Auckl)       Date:  2015-06-03

Review 2.  Practical considerations in clinical strategy to support the development of injectable drug-device combination products for biologics.

Authors:  Zhaoyang Li; Rachael Easton
Journal:  MAbs       Date:  2017-11-07       Impact factor: 5.857

3.  User-Centric Approach to Specifying Technical Attributes of Drug Delivery Devices: Empirical Study of Autoinjector-Cap Removal Forces.

Authors:  Andreas Schneider; Philipp Richard; Philippe Mueller; Christoph Jordi; Mary Yovanoff; Jakob Lange
Journal:  Patient Prefer Adherence       Date:  2021-02-02       Impact factor: 2.711

4.  Sustained in vitro interferon-beta release and in vivo toxicity of PLGA and PEG-PLGA nanoparticles.

Authors:  Andrea Fodor-Kardos; Ádám Ferenc Kiss; Katalin Monostory; Tivadar Feczkó
Journal:  RSC Adv       Date:  2020-04-22       Impact factor: 4.036

Review 5.  Profile of PEGylated interferon beta in the treatment of relapsing-remitting multiple sclerosis.

Authors:  Eleonora Cocco; Maria Giovanna Marrosu
Journal:  Ther Clin Risk Manag       Date:  2015-05-08       Impact factor: 2.423

6.  Long-Term Adherence to IFN Beta-1a Treatment when Using RebiSmart® Device in Patients with Relapsing-Remitting Multiple Sclerosis.

Authors:  O Fernández; R Arroyo; S Martínez-Yélamos; M Marco; J A García Merino; D Muñoz; E Merino; A Roque
Journal:  PLoS One       Date:  2016-08-15       Impact factor: 3.240

  6 in total

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