Abstract | BACKGROUND: There are currently very few drugs available to directly treat diabetic complications. Those that are indicated clinically provide symptomatic relief and do not address the underlying biochemical problems. The involvement of the sorbitol pathway in complications has provided mechanistic insights into the biochemistry of complications and the key enzyme, aldose reductase, has become an attractive pharmacologic target. OBJECTIVE: METHODS: A survey of in vitro and in vivo studies was conducted, and with publicly available data from clinical trials, ranirestat efficacy was compared with other similar agents. RESULTS/CONCLUSION:
Ranirestat is safe, exhibits some efficacy and is perhaps the only agent advanced enough in clinical trials to warrant further consideration for diabetic complications.
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Authors | Nick Giannoukakis |
Journal | Expert opinion on investigational drugs
(Expert Opin Investig Drugs)
Vol. 17
Issue 4
Pg. 575-81
(Apr 2008)
ISSN: 1744-7658 [Electronic] England |
PMID | 18363521
(Publication Type: Journal Article, Review)
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Chemical References |
- Enzyme Inhibitors
- Pyrazines
- Spiro Compounds
- Sorbitol
- Aldehyde Reductase
- ranirestat
|
Topics |
- Aldehyde Reductase
(antagonists & inhibitors, metabolism)
- Animals
- Clinical Trials as Topic
- Diabetes Complications
(drug therapy, enzymology, prevention & control)
- Diabetes Mellitus
(drug therapy, enzymology)
- Enzyme Inhibitors
(adverse effects, therapeutic use)
- Humans
- Pyrazines
(adverse effects, therapeutic use)
- Sorbitol
(metabolism)
- Spiro Compounds
(adverse effects, therapeutic use)
- Treatment Outcome
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