SwePub
Sök i LIBRIS databas

  Utökad sökning

WFRF:(Kijima Shinichi)
 

Sökning: WFRF:(Kijima Shinichi) > (2015-2019) > Applications of Cli...

Applications of Clinically Relevant Dissolution Testing : Workshop Summary Report

Suarez-Sharp, Sandra (författare)
US FDA, Div Biopharmaceut, Off New Drug Prod, Off Pharmaceut Qual,Ctr Drug Evaluat & Res, Silver Spring, MD 20993 USA
Cohen, Michael (författare)
Pfizer Inc, Eastern Point Rd, Groton, CT 06340 USA
Kesisoglou, Filippos (författare)
Merck & Co Inc, Pharmaceut Sci, 770 Sumneytown Pike, West Point, PA 19486 USA
visa fler...
Abend, Andreas (författare)
Merck & Co Inc, Pharmaceut Sci, 770 Sumneytown Pike, West Point, PA 19486 USA
Marroum, Patrick (författare)
Abbvie Inc, 1 North Waukegan Rd North, Chicago, IL 60064 USA
Delvadia, Poonam (författare)
US FDA, Div Biopharmaceut, Off New Drug Prod, Off Pharmaceut Qual,Ctr Drug Evaluat & Res, Silver Spring, MD 20993 USA
Kotzagiorgis, Evangelos (författare)
EMA, Specialized Disciplines Dept, Human Med Res & Dev Support Div, 30 Churchill Pl, London E14 5EU, England
Li, Min (författare)
US FDA, Div Biopharmaceut, Off New Drug Prod, Off Pharmaceut Qual,Ctr Drug Evaluat & Res, Silver Spring, MD 20993 USA
Nordmark, Anna (författare)
MPA, Dept Efficacy & Safety 2, Uppsala, Sweden
Bandi, Nagesh (författare)
Merck & Co Inc, Pharmaceut Sci, 770 Sumneytown Pike, West Point, PA 19486 USA
Sjögren, Erik, 1977- (författare)
Uppsala universitet,Institutionen för farmaci,Pharmetheus, S-75237 Uppsala, Sweden
Babiskin, Andrew (författare)
US FDA, Div Quantitat Methods & Modeling, Off Res & Stand, Off Gener Drugs, Silver Spring, MD USA
Heimbach, Tycho (författare)
Novartis Pharmaceut, One Hlth Plaza, E Hanover, NJ 07936 USA
Kijima, Shinichi (författare)
PMDA, Adv Review Elect Data Promot Grp, Tokyo, Japan
Mandula, Haritha (författare)
US FDA, Div Biopharmaceut, Off New Drug Prod, Off Pharmaceut Qual,Ctr Drug Evaluat & Res, Silver Spring, MD 20993 USA
Raines, Kimberly (författare)
US FDA, Div Biopharmaceut, Off New Drug Prod, Off Pharmaceut Qual,Ctr Drug Evaluat & Res, Silver Spring, MD 20993 USA
Seo, Paul (författare)
US FDA, Div Biopharmaceut, Off New Drug Prod, Off Pharmaceut Qual,Ctr Drug Evaluat & Res, Silver Spring, MD 20993 USA
Zhang, Xinyuan (författare)
US FDA, Off Clin Pharmacol, Off Translat Sci, Ctr Drug Evaluat & Res, Silver Spring, MD USA
visa färre...
 (creator_code:org_t)
2018-08-27
2018
Engelska.
Ingår i: AAPS Journal. - : SPRINGER. - 1550-7416. ; 20:6
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • This publication summarizes the proceedings of day 3 of a 3-day workshop on "Dissolution and Translational Modeling Strategies Enabling Patient-Centric Product Development." Specifically, this publication discusses the current approaches in building clinical relevance into drug product development for solid oral dosage forms, along with challenges that both industry and regulatory agencies are facing in setting clinically relevant drug product specifications (CRDPS) as presented at the workshop. The concept of clinical relevance is a multidisciplinary effort which implies an understanding of the relationship between the critical quality attributes (CQAs) and their impact on predetermined clinical outcomes. Developing this level of understanding, in many cases, requires introducing deliberate but meaningful variations into the critical material attributes (CMAs) and critical process parameters (CPPs) to establish a relationship between the resulting in vitro dissolution/release profiles and in vivo PK performance, a surrogate for clinical outcomes. Alternatively, with the intention of improving the efficiency of the drug product development process by limiting the burden of conducting in vivo studies, this understanding can be either built, or at least enhanced, through in silico efforts, such as IVIVC and physiologically based pharmacokinetic (PBPK) absorption modeling and simulation (M&S). These approaches enable dissolution testing to establish safe boundaries and reject drug product batches falling outside of the established safe range (e.g., due to inadequate in vivo performance) enabling the method to become clinically relevant. Ultimately, these efforts contribute towards patient-centric drug product development and allow regulatory flexibility throughout the lifecycle of the drug product.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmakologi och toxikologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmacology and Toxicology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmaceutiska vetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmaceutical Sciences (hsv//eng)

Nyckelord

clinically relevant specifications
dissolution
IVIVC/IVIVR
PBPK absorption modeling and simulation
safe space

Publikations- och innehållstyp

ref (ämneskategori)
art (ämneskategori)

Hitta via bibliotek

Till lärosätets databas

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy