Table 3.
Treatment | Preclinical experimental | Administration | Phase I | Phase II | Phase III | Marketing authorization |
---|---|---|---|---|---|---|
Tafamidis* | – | Oral | 2007 | −>2009 | EMA : November 2011 ANSM: September 2011 FDA: No | |
Diflunisal$ | – | Oral | −>2010 | |||
DOXY-TUDCA‡ | + | Oral | Current | |||
ASOs§ | + | SCI | Current | 2013 | ||
SiRNA¶ | + | IVI | 2011–2012 | 2012 | 2013? | |
Anti-SAP Mab# | + | IVI | 2013? |
Coelho et al. [2012]; $ Berk et al. [2011]; ‡ Cardoso et al. [2010], Obici et al. [2012]; § Ackermann et al. [2012], Benson et al. [2006]; ¶ Coelho et al. [2011]; # Bodin et al. [2010].
ANSM, Agence nationale de sécurité du médicmanet et des produits de santé; ASO, antisense oligonucleotide; DOXY-TUDCA, doxycycline taurodesoxycholic acid; EMA, European Medicines Agency; FDA, US Food and Drug Administration; IVI, intravenous infusion; SCI, subcutaneous injection.