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Current Approaches to Design Space Development and Regulatory Applications for Drug Products: Findings from the IQ Utilization of Design Space for Filings Working Group Survey.
Miesle, James E; Osei-Yeboah, Frederick; Pauli-Bruns, Anette; Chen, Bei; Manceva, Slobodanka; Wade, Jonathan B; Yin, Shawn; Desai, Divyakant; Dirat, Olivier; Bhugra, Chandan; Stauffer, Fanny.
Afiliación
  • Miesle JE; Synthetic Molecule Design and Development, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN, 46285, USA. miesleje@lilly.com.
  • Osei-Yeboah F; Pharmaceutical Development, Biogen, Cambridge, MA, USA.
  • Pauli-Bruns A; Biologics Drug Product Development, Sanofi, Frankfurt, Germany.
  • Chen B; Product Development Science & Technology, Abbvie, North Chicago, IL, USA.
  • Manceva S; Biologics Drug Product Development, Teva Branded Pharmaceuticals, West Chester, PA, USA.
  • Wade JB; Technical Services/Manufacturing Science, Eli Lilly and Company, Indianapolis, IN, USA.
  • Yin S; Drug Product Development, BMS, New Brunswick, NJ, USA.
  • Desai D; Drug Product Development, BMS, New Brunswick, NJ, USA.
  • Dirat O; Global Regulatory Sciences - CMC Advisory Office, Pfizer, Sandwich, UK.
  • Bhugra C; Drug Product Development, GSK, Collegeville, PA, USA.
  • Stauffer F; UCB Pharma, Brussels, Belgium.
Pharm Res ; 41(9): 1775-1786, 2024 Sep.
Article en En | MEDLINE | ID: mdl-39231907
ABSTRACT

PURPOSE:

The concept of a Design Space (DSp) was introduced in ICH Q8 as a tool within the quality-by-design (QbD) approach to pharmaceutical development with the intent of being globally applicable. However, there appears to be variance in the regulatory agency expectations in pharmaceutical product filing and implementation of DSp. This paper presents some of the current industry perspective on design space.

METHODS:

The Utilization of Design Space for Filings (UDSpF) Working Group in the Innovation and Quality (IQ) Consortium conducted a survey to establish a baseline for the current understanding of DSp among IQ member companies and assess the similarities and/or differences in strategies when filing a DSp. The survey focused on how IQ member companies approach DSp development, the primary drivers for the DSp, the presentation of the DSp in the filing, DSp verification and the benefits and flexibility anticipated and/or realized.

RESULTS:

A total of 14 responses were received and analyzed representing a small sample size but a large proportion of the innovator industry/large pharmaceutical companies. The survey results revealed that DSp is not yet a commonplace for small molecule drug products and may not even be utilized as much in large molecule drug products. The benefits of DSp, with respect to enhanced process understanding, are well understood by the sponsors; however, the benefits of filed DSp with respect to manufacturing flexibility are not fully realized in the commercial lifecycle of the product. There are also challenges in gaining consistent buy-in/value proposition for DSp among cross-functional teams within organizations.

CONCLUSIONS:

There are still gaps in design space implementation for its full benefit in the pharmaceutical industry. The WG has presented a unified view from member companies on the approach to DSp considering when/where the DSp experiments are conducted and on the extent of the DSp development proposed in a dossier.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Industria Farmacéutica / Desarrollo de Medicamentos Límite: Humans Idioma: En Revista: Pharm Res Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Industria Farmacéutica / Desarrollo de Medicamentos Límite: Humans Idioma: En Revista: Pharm Res Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos