• Je něco špatně v tomto záznamu ?

Beyond Reimbursement Status: Availability of Advanced Therapy Medicinal Products Across the European Union

Z. Čechová, J. Kubátová, A. Bártová, J. Jamárik, J. Samek

. 2025 ; 59 (4) : 728-736. [pub] 20250410

Jazyk angličtina Země Švýcarsko

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc25015204

Grantová podpora
101059788 Horizon Europe Coordination and Support Action

BACKGROUND: Advanced Therapy Medicinal Products (ATMPs) represent an innovative therapeutic approach with the potential to impact the treatment of rare diseases significantly. Although authorised centrally in the European Union, their market launch differs across Member States (MS). This study aimed to describe the ATMP market availability in MS and explore potential influencing factors, providing insights into specific barriers beyond pricing and reimbursement policies. METHODS: ATMP availability was defined as the product launch in each MS. Data was collected through open governmental sources, databases, and communication with national competent authorities. Spearman's correlation coefficients were calculated to examine the relationship between ATMP availability and their characteristics (time since granting marketing authorisation, target patient population size, and cost). RESULTS: We collected the availability data on 18 ATMPs from 23 EU MS. Market uptake varied significantly, with Germany (89%), France and Italy (61%) leading. Estonia and Latvia confirmed that no ATMP has been launched on their markets yet. Six ATMPs were available in more than one-third of the analysed MS. No significant correlation was observed between ATMP availability and analysed product characteristics except for time dependency for CAR T-cell therapies. CONCLUSION: Beyond pricing and reimbursement processes, the ATMP commercialisation in particular MS is influenced by the marketing authorisation holder's decision and capacity. ATMPs face product-specific challenges in achieving EU-wide availability, including complex manufacturing, distribution, and administration processes. To increase the accessibility of innovative ATMP-based treatments, implementing the cross-border access framework or individual ATMP production under the hospital exemption is essential, especially in underserved MS.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc25015204
003      
CZ-PrNML
005      
20250731090830.0
007      
ta
008      
250708s2025 sz f 000 0|eng||
009      
AR
024    7_
$a 10.1007/s43441-025-00769-z $2 doi
035    __
$a (PubMed)40208421
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a sz
100    1_
$a Čechová, Zora $u Centre of Excellence CREATIC, Faculty of Medicine, Masaryk University, Kamenice 5, Brno, 62500, Czech Republic. zora.cechova@med.muni.cz
245    10
$a Beyond Reimbursement Status: Availability of Advanced Therapy Medicinal Products Across the European Union / $c Z. Čechová, J. Kubátová, A. Bártová, J. Jamárik, J. Samek
520    9_
$a BACKGROUND: Advanced Therapy Medicinal Products (ATMPs) represent an innovative therapeutic approach with the potential to impact the treatment of rare diseases significantly. Although authorised centrally in the European Union, their market launch differs across Member States (MS). This study aimed to describe the ATMP market availability in MS and explore potential influencing factors, providing insights into specific barriers beyond pricing and reimbursement policies. METHODS: ATMP availability was defined as the product launch in each MS. Data was collected through open governmental sources, databases, and communication with national competent authorities. Spearman's correlation coefficients were calculated to examine the relationship between ATMP availability and their characteristics (time since granting marketing authorisation, target patient population size, and cost). RESULTS: We collected the availability data on 18 ATMPs from 23 EU MS. Market uptake varied significantly, with Germany (89%), France and Italy (61%) leading. Estonia and Latvia confirmed that no ATMP has been launched on their markets yet. Six ATMPs were available in more than one-third of the analysed MS. No significant correlation was observed between ATMP availability and analysed product characteristics except for time dependency for CAR T-cell therapies. CONCLUSION: Beyond pricing and reimbursement processes, the ATMP commercialisation in particular MS is influenced by the marketing authorisation holder's decision and capacity. ATMPs face product-specific challenges in achieving EU-wide availability, including complex manufacturing, distribution, and administration processes. To increase the accessibility of innovative ATMP-based treatments, implementing the cross-border access framework or individual ATMP production under the hospital exemption is essential, especially in underserved MS.
650    _2
$a Evropská unie $7 D005062
650    _2
$a vzácné nemoci $x terapie $7 D035583
650    12
$a dávkové mechanismy $7 D012051
655    _2
$a časopisecké články $7 D016428
700    1_
$a Kubátová, Jana $u Centre of Excellence CREATIC, Faculty of Medicine, Masaryk University, Kamenice 5, Brno, 62500, Czech Republic
700    1_
$a Bártová, Adéla $u Centre of Excellence CREATIC, Faculty of Medicine, Masaryk University, Kamenice 5, Brno, 62500, Czech Republic $u Department of Pharmacology, Faculty of Medicine, Masaryk University, Brno, Czech Republic
700    1_
$a Jamárik, Jakub $u Centre of Excellence CREATIC, Faculty of Medicine, Masaryk University, Kamenice 5, Brno, 62500, Czech Republic
700    1_
$a Samek, Jiří $u Centre of Excellence CREATIC, Faculty of Medicine, Masaryk University, Kamenice 5, Brno, 62500, Czech Republic
773    0_
$w MED00198808 $t Therapeutic innovation & regulatory science $x 2168-4804 $g Roč. 59, č. 4 (2025), s. 728-736
856    41
$u https://pubmed.ncbi.nlm.nih.gov/40208421 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y - $z 0
990    __
$a 20250708 $b ABA008
991    __
$a 20250731090824 $b ABA008
999    __
$a ok $b bmc $g 2366201 $s 1252329
BAS    __
$a 3
BAS    __
$a PreBMC-MEDLINE
BMC    __
$a 2025 $b 59 $c 4 $d 728-736 $e 20250410 $i 2168-4804 $m Therapeutic innovation & regulatory science $n Ther Innov Regul Sci $x MED00198808
GRA    __
$a 101059788 $p Horizon Europe Coordination and Support Action
LZP    __
$a Pubmed-20250708

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...