2015
DOI: 10.1186/s12967-015-0517-x
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Preclinical good laboratory practice-compliant safety study to evaluate biodistribution and tumorigenicity of a cartilage advanced therapy medicinal product (ATMP)

Abstract: BackgroundThe clinical development of advanced therapy medicinal products (ATMPs), a new class of drugs, requires initial safety studies that deviate from standard non-clinical safety protocols. The study provides a strategy to address the safety aspects of biodistribution and tumorigenicity of ATMPs under good laboratory practice (GLP) conditions avoiding cell product manipulation. Moreover, the strategy was applied on a human ATMP for cartilage repair.MethodsThe testing strategy addresses biodistribution and… Show more

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Cited by 24 publications
(17 citation statements)
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“…These results argue for an advantage of cell-loaded versus cell-free collagen implants, in agreement with earlier studies on cellseeded or cell-containing implants based on collagen or other cartilage replacement materials. [41][42][43][44] Alternatively, in vivo microfracturing of the subchondral bone plate below the cartilage implant can be used to favor cell immigration into initially cell-free implants and optimize the conditions for successful cartilage repair. 39,40,45 Cell-free and cell-loaded collagen implants both showed progressive deposition of the matrix molecule aggrecan and a stable protein content of collagen 2 throughout culture, again demonstrating the cytocompatibility of the implant material and the active production of cartilage-specific matrix molecules by vital chondrocytes.…”
Section: Discussionmentioning
confidence: 99%
“…These results argue for an advantage of cell-loaded versus cell-free collagen implants, in agreement with earlier studies on cellseeded or cell-containing implants based on collagen or other cartilage replacement materials. [41][42][43][44] Alternatively, in vivo microfracturing of the subchondral bone plate below the cartilage implant can be used to favor cell immigration into initially cell-free implants and optimize the conditions for successful cartilage repair. 39,40,45 Cell-free and cell-loaded collagen implants both showed progressive deposition of the matrix molecule aggrecan and a stable protein content of collagen 2 throughout culture, again demonstrating the cytocompatibility of the implant material and the active production of cartilage-specific matrix molecules by vital chondrocytes.…”
Section: Discussionmentioning
confidence: 99%
“…In contrast, subcutaneous implantation is an easy and non-invasive technique, and allows performance of several test items in the same animal [27]. …”
Section: Discussionmentioning
confidence: 99%
“…[23][24][25][26][27][28] Although the rules and regulations remain unclear, clinicians that are interested should carry-on with the best available guidelines to ensure safety and compliance during delivery in clinical practice to avoid regulatory infraction. 29 While ill-defined regulation encourages experimentation and novel clinical application, efficacy and patient safety concerns are a real concern.…”
Section: Regulatory Implications Facing Cartilage Regenerative Medicinementioning
confidence: 99%