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# HIV/AIDS Update - Changes to the Trivicay (dolutegravir) product labeling
- URL: https://www.foodconsumer.org/trivicay_0516140444/
- Published: 2014-05-16T17:44:00.000Z
- Updated: 2026-09-15T14:09:33.000Z
- Description: FDA approved labeling updates for Tivicay (dolutegravir) covering its effects on renal transporters and interactions with calcium carbonate and ferrous fumarate. The new text notes dolutegravir inhibits OCT2 and MATE1 and may raise levels of drugs cleared by those transporters.
- Author: Food Consumer
- Tags: Miscellaneous, Health News, #vivvo-import

On May 12, 2014, FDA approved updates to the TIVICAY (dolutegravir) product labeling with information regarding the effect of dolutegravir on renal transporters and drug-drug interaction data between dolutegravir and calcium carbonate or ferrous fumarate.

Section 7.1 *Effect of Dolutegravir on the Pharmacokinetics of Other Agents*, subsection was updated as follows:In vitro, dolutegravir inhibited the renal organic cation transporters, OCT2 (IC50\=1.93 µM) and multidrug and toxin extrusion transporter (MATE) 1 (IC50 \= 6.34 mM). In vivo, dolutegravir inhibits tubular secretion of creatinine by inhibiting OCT2and potentially MATE1\. Dolutegravir may increase plasma concentrations of drugs eliminated via OCT2 or MATE1 (dofetilide and metformin, Table 5) *\[see Contraindications (4), Drug Interactions (7.3)\].* In vitro, dolutegravir inhibited the basolateral renal transporters, organic anion transporter (OAT) 1 (IC50 \= 2.12 mM) and OAT3 (IC50 \= 1.97 mM). However, in vivo, dolutegravir did not alter the plasma concentrations of tenofovir or paraaminohippurate, substrates of OAT1 and OAT3\. In vitro, dolutegravir did not inhibit (IC50 \>50 μM) the following: cytochrome P450 (CYP)1A2, CYP2A6, CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP2D6, CYP3A, UGT1A1, UGT2B7, P-glycoprotein (P-gp), breast cancer resistance protein (BCRP), bile salt export pump (BSEP), organic anion transporter polypeptide (OATP)1B1, OATP1B3, OCT1, multidrug resistance protein (MRP)2 or MRP4\. In vitro, dolutegravir did not induce CYP1A2, CYP2B6, or CYP3A4\. Based on these data and the results of drug interaction trials, dolutegravir is not expected to affect the pharmacokinetics of drugs that are substrates of these enzymes or transporters. Additionally, in section 7: *Drug Interactions*, Table 5 – the following was added regarding co administration with oral calcium or iron supplements, including multivitamins containing calcium or iron:TIVICAY should be administered 2 hours before or 6 hours after taking supplements containing calcium or iron. Alternatively, TIVICAY and supplements containing calcium or iron can be taken together with food. The complete revised label can be viewed at this [Drugs@FDA](http://links.govdelivery.com/track?type=click&enid=ZWFzPTEmbWFpbGluZ2lkPTIwMTQwNTE2LjMyMjY3NjcxJm1lc3NhZ2VpZD1NREItUFJELUJVTC0yMDE0MDUxNi4zMjI2NzY3MSZkYXRhYmFzZWlkPTEwMDEmc2VyaWFsPTE2ODMyODczJmVtYWlsaWQ9Zm9vZGNvbnN1bWVyLm9yZ0BnbWFpbC5jb20mdXNlcmlkPWZvb2Rjb25zdW1lci5vcmdAZ21haWwuY29tJmZsPSZleHRyYT1NdWx0aXZhcmlhdGVJZD0mJiY=&&&100&&&http://www.accessdata.fda.gov/drugsatfda%5Fdocs/label/2014/204790s001lbl.pdf?source=govdelivery&utm%5Fmedium=email&utm%5Fsource=govdelivery) link. Tivicay is a human immunodeficiency virus type 1 (HIV-1) integrase strand transfer inhibitor (INSTI) indicated in combination with other antiretroviral agents for the treatment of HIV-1 infection in adults and children aged 12 years and older and weighing at least 40 kg,marketed by GlaxoSmithKline. 

Richard Klein  
Office of Health and Constituent Affairs  
Food and Drug Administration  
  
Kimberly Struble  
Division of Antiviral Products  
Food and Drug Administration  
  
Steve Morin  
Office of Health and Constituent Affairs  
Food and Drug Administration