Clinical data | |
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Trade names | Amitiza |
Other names | RU-0211 SPI-0211 |
AHFS/Drugs.com | Monograph |
MedlinePlus | a607034 |
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Routes of administration | By mouth |
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Pharmacokinetic data | |
Bioavailability | Negligible |
Protein binding | 94% |
Metabolism | Extensive, CYP not involved |
Elimination half-life | Unknown (lubiprostone) 0.9–1.4 hours (main metabolite) |
Excretion | Kidney (60%) and fecal (30%) |
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CompTox Dashboard (EPA) | |
ECHA InfoCard | 100.107.168 |
Chemical and physical data | |
Formula | C20H32F2O5 |
Molar mass | 390.468 g·mol−1 |
3D model (JSmol) | |
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Lubiprostone, sold under the brand name Amitiza among others, is a medication used in the management of chronic idiopathic constipation, predominantly irritable bowel syndrome-associated constipation in women and opioid-induced constipation. The drug is owned by Mallinckrodt and is marketed by Takeda Pharmaceutical Company.
The drug was developed by Sucampo Pharmaceuticals and approved by the Food and Drug Administration (FDA) in 2006.[2][3][4] It was recommended for use in the UK by the National Institute for Health and Care Excellence (NICE) in July 2014.[5] Health Canada approved the drug in 2015.[6] Lubiprostone received approval from the Food and Drug Administration in 2008, to treat irritable bowel syndrome with constipation (IBS-C),[7] and in 2013, for the treatment of opioid-induced constipation in adults with chronic noncancer pain.[4] It is available as a generic medication.[8]