{"id":36208,"date":"2019-06-19T08:36:49","date_gmt":"2019-06-19T08:36:49","guid":{"rendered":"http:\/\/i-base.info\/htb\/?p=36208"},"modified":"2019-06-19T09:56:45","modified_gmt":"2019-06-19T09:56:45","slug":"efavirenz-600-mg-exposure-appears-sufficient-with-high-dose-daily-rifapentine","status":"publish","type":"post","link":"https:\/\/i-base.info\/htb\/36208","title":{"rendered":"Efavirenz 600 mg exposure appears sufficient with high-dose daily rifapentine"},"content":{"rendered":"<p><strong>Polly Clayden, HIV i-Base<\/strong><\/p>\n<p><strong>Preliminary pharmacokinetic (PK) data support starting efavirenz (EFV)-based ART during TB treatment with high-dose daily rifapentine (RPT). These findings were presented at the 20th International Workshop on Clinical Pharmacology of HIV, Hepatitis, and Other Antiviral Drugs.<\/strong><\/p>\n<p>The Tuberculosis Trials Consortium Study 31 (S31)\/AIDS Clinical Trials Group Study A5349 is a phase 3 trial comparing two short-course TB treatment regimens including high dose daily RPT to standard TB treatment.<\/p>\n<p>RPT is a CYP inducer and EFV is a CYP substrate, so there is a potential risk of decreased EFV exposure with co-administration. A secondary objective and sub study of S31\/A5349 was to look at the effect of RPT on EFV PK in treatment-naive participants starting EFV-based ART while receiving RPT-based TB treatment.<\/p>\n<p>This sub study included participants starting EFV-based (600mg) ART within the first 9 weeks of TB treatment, randomised to one of two regimens containing daily RPT (1200mg), isoniazid (H), pyrazinamide and either ethambutol or moxifloxacin.<\/p>\n<p>Data were presented for 28 evaluable participants: 25% women, 96% black\/African, median age 36 years and mean baseline CD4 count 252 cells\/mm3.<\/p>\n<p>Median EFV concentrations approximately 4 and 8 weeks after starting EFV were: 2.76 (IQR 2.12 to 4.67) mg\/L and 2.86 (IQR 2.19 to 4.88) mg\/L respectively. EFV concentrations at week 22 (after TB treatment completed) were: 2.86 (IQR 1.93-4.21) mg\/L.<\/p>\n<p>The protocol specified that at least 80% of participants must have EFV concentrations &gt;1 mg\/L at both time points during TB treatment in order to continue enrolment.<\/p>\n<p>The percentage of participants with EFV concentrations &gt;1 mg\/L at 4 and 8 weeks after starting EFV were: 25\/28 (89%) and 26\/28 (93%). At week 22 19\/21 (90%) of participants had EFV concentrations &gt;1mg\/L.<\/p>\n<p>Median EFV CL\/F were: 7.28 (IQR 5.47 to 10.08) and 8.3 (IQR 6.17 to 10.66) L\/hr during and post RPT\/H respectively.<\/p>\n<p>The GMR of during to post RPT\/H EFV CL\/F was 0.89 (90% CI 0.64 to 1.23). Median baseline viral load (n=25) was 81,003 copies\/mL; 20\/23 (87%) participants had undetectable viral load at week 22.<\/p>\n<p>These data provide preliminary support for initiating EFV-containing ART during co-administration of daily high-dose RPT for TB treatment.<\/p>\n<p>This presentation included a summary of ongoing investigations and knowledge gaps in the use of RPT DDI with ART. See Table 1.<\/p>\n<p><strong>Table 1. Gaps in RPT DDI pharmacology<\/strong><\/p>\n<table>\n<tbody>\n<tr>\n<td width=\"61\"><strong>LTBI <\/strong><\/td>\n<td width=\"58\"><strong>Compatible ART<\/strong><\/td>\n<td width=\"78\"><strong>DDI trial status<\/strong><\/td>\n<td width=\"85\"><strong>Results expected<\/strong><\/td>\n<td width=\"85\"><strong>Knowledge gaps<\/strong><\/td>\n<\/tr>\n<tr>\n<td width=\"61\">3HP<\/td>\n<td width=\"58\">EFV<br \/>\nRAL 400 mg BID DTG<\/td>\n<td width=\"78\">3HP w\/ TAF in HV (Yoda) enrolling<\/td>\n<td width=\"85\">Final 2020<\/td>\n<td width=\"85\">3HP + TAF in HIV+<\/td>\n<\/tr>\n<tr>\n<td width=\"61\">1HP<\/td>\n<td width=\"58\">EFV<\/td>\n<td width=\"78\">ACTG A5372<\/td>\n<td width=\"85\">Initial PK 2020<\/td>\n<td width=\"85\">DTG (what dose?) TAF<\/td>\n<\/tr>\n<tr>\n<td width=\"61\">TB treatment<\/td>\n<td width=\"58\">Compatible ART<\/td>\n<td width=\"78\">DDI trial status<\/td>\n<td width=\"85\">Results expected<\/td>\n<td width=\"85\">Knowledge gaps<\/td>\n<\/tr>\n<tr>\n<td width=\"61\">RPT x 17 weeks (S31)<\/td>\n<td width=\"58\">EFV<\/td>\n<td width=\"78\">S31\/A5349<\/td>\n<td width=\"85\">Final PK results late 2019<\/td>\n<td width=\"85\">DTG TAF<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>Key: DDI drug drug interaction; DTG, dolutegravir; EFV, efavirenz; LTBI, latent TB infection; PK, pharmacokinetics; RAL, raltegravir; RPT, rifapentine; TAF, tenofovir alafenamide; 1HP, one month isoniazid\/rifapentine; 3HP, three month isoniazid\/rifapentine.<\/p>\n<p><em>Adapted from Swindells and Dooley <\/em><\/p>\n<p>Reference<\/p>\n<p>Podany A et al. Efavirenz pharmacokinetics in HIV\/TB coinfected persons initiating ART while receiving high dose rifapentine. 20th International Workshop on Clinical Pharmacology of HIV, Hepatitis, and Other Antiviral Drugs. \u00a014\u201316 May 2019, Noordwijk, the Netherlands.\u00a0Oral abstract 1.<br \/>\n<a href=\"http:\/\/regist2.virology-education.com\/presentations\/2019\/20AntiviralPK\/07_Podany.pdf\" rel=\"noopener\">http:\/\/regist2.virology-education.com\/presentations\/2019\/20AntiviralPK\/07_Podany.pdf<\/a> (PDF slides)<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Polly Clayden, HIV i-Base Preliminary pharmacokinetic (PK) data support starting efavirenz (EFV)-based ART during TB treatment with high-dose daily rifapentine (RPT). These findings were presented at the 20th International Workshop on Clinical Pharmacology of HIV, Hepatitis, and Other Antiviral Drugs. &hellip;<\/p>\n","protected":false},"author":3,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[4,34,37],"tags":[268],"class_list":["post-36208","post","type-post","status-publish","format-standard","hentry","category-conference-reports","category-pk-and-drug-interactions","category-tb-coinfection","tag-pk-workshop-2019"],"_links":{"self":[{"href":"https:\/\/i-base.info\/htb\/wp-json\/wp\/v2\/posts\/36208","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/i-base.info\/htb\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/i-base.info\/htb\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/i-base.info\/htb\/wp-json\/wp\/v2\/users\/3"}],"replies":[{"embeddable":true,"href":"https:\/\/i-base.info\/htb\/wp-json\/wp\/v2\/comments?post=36208"}],"version-history":[{"count":0,"href":"https:\/\/i-base.info\/htb\/wp-json\/wp\/v2\/posts\/36208\/revisions"}],"wp:attachment":[{"href":"https:\/\/i-base.info\/htb\/wp-json\/wp\/v2\/media?parent=36208"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/i-base.info\/htb\/wp-json\/wp\/v2\/categories?post=36208"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/i-base.info\/htb\/wp-json\/wp\/v2\/tags?post=36208"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}