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. Author manuscript; available in PMC: 2020 Mar 20.
Published in final edited form as: Trends Pharmacol Sci. 2019 Sep 10;40(10):790–800. doi: 10.1016/j.tips.2019.08.006

Table 1.

FDA and PMDA approval of SLC drugs from 2015 to 2018.

aSLC bOther name cDrug dYear Indication Mechanism of action References / Resources
SLC10A2 ASBT Elobixibate
(A3309)
2018 Chronic idiopathic constipation Increases bile acid delivery to colon to accelerate and increase colonic secretion. [8]
SLC5A2 SGLT2 SteglatroTM
(ertugliflozin)
2017 Type II diabetes mellitus Increases urinary glucose excretion via SGLT2 inhibition to reduce blood glucose levels. iv
SLC18A2 VMAT2 Ingrezza™
(valbenazine)
2017 Tardive dyskinesia Reversible inhibition of VMAT2 activity. v
SLC18A2 VMAT2 Austedo™
(deutetrabenazine)
2017 Chorea associated with Huntington’s disease; Tardive dyskinesia Mechanism of action for anti-chorea effects is currently unknown. vi
SLC22A12 URAT1 Zurampic™
(lesinurad)
2015 Hyperuricemia associated with gout Inhibition of URAT1 and organic anion transporter 4 (OAT4) (to a lesser extent), to increase uric acid excretion and reduce serum uric acid levels. vii
a

SLC marks the primary SLC target of the newly approved drug

b

Other name corresponds to alternative name of the SLC gene or protein

c

Drug is the brand name of the drug with the generic name in parenthesis

d

Year marks the approval year of the drug by the FDA

e

Elobixibat is a PMDA-approved drug. All others are FDA-approved.