Investigational Antiretroviral Drugs: What is Coming Down the Pipeline.

Q1 Medicine Topics in antiviral medicine Pub Date : 2018-04-01
Roy M Gulick
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Abstract

Over the past 30 years, antiretroviral drug regimens for treating HIV infection have become more effective, safer, and more convenient. Despite 31 currently approved drugs, the pipeline of investigational HIV drugs remains full. Investigational antiretroviral drugs include the nucleoside analogue reverse transcriptase translocation inhibitor (NRTTI) MK-8591, a long-acting compound that could be dosed once weekly. Investigational nonnucleoside analogue reverse transcriptase inhibitors (NNRTIs) include doravirine, which is active in vitro against NNRTI-resistant HIV and was potent and well-tolerated when used in combination with a dual-nucleoside analogue RTI (nRTI) backbone in treatment-naive individuals.New integrase strand transfer inhibitors (InSTIs) include recently approved bictegravir, which is active against InSTI-resistant viral strains in vitro and was potent and well-tolerated in combination regimens in treatment-naive individuals, and investigational cabotegravir, which is being studied with monthly parenteral dosing for HIV maintenance treatment and with bimonthly dosing for HIV preexposure prophylaxis (PrEP). Investigational HIV entry inhibitors include the new CD4 attachment inhibitor fostemsavir, which targets HIV envelope glycoprotein 120, and recently approved ibalizumab, which binds the CD4 receptor. This article summarizes presentations by Roy M. Gulick, MD, MPH, at the IAS-USA continuing education program, Improving the Management of HIV Disease, held in Los Angeles, California, in April 2017, and at the 2017 Ryan White HIV/AIDS Program Clinical Conference, held in San Antonio, Texas, in August 2017.

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正在研究的抗逆转录病毒药物:即将问世的药物。
在过去的30年里,用于治疗艾滋病毒感染的抗逆转录病毒药物方案变得更有效、更安全、更方便。尽管目前有31种药物获得批准,但用于艾滋病研究的药物仍然很充足。正在研究的抗逆转录病毒药物包括核苷类似物逆转录酶易位抑制剂(NRTTI) MK-8591,这是一种长效化合物,可以每周给药一次。正在研究的非核苷类似物逆转录酶抑制剂(NNRTIs)包括多拉韦林,它在体外对nnrti耐药的HIV有活性,当与双核苷类似物RTI (nRTI)主干联合使用时,在未接受治疗的个体中具有强效和良好的耐受性。新的整合酶链转移抑制剂(insi)包括最近批准的比替格雷韦(bictegravir)和卡替格雷韦(cabotegravir),前者在体外对insi耐药的病毒株有效,并且在首次治疗的个体中具有有效和良好的耐受性,后者正在研究每月给药用于HIV维持治疗和每月给药用于HIV暴露前预防(PrEP)。正在研究的HIV进入抑制剂包括针对HIV包膜糖蛋白120的新型CD4附着抑制剂fostemsavir,以及最近批准的结合CD4受体的ibalizumab。本文总结了Roy M. Gulick医学博士、公共卫生硕士在2017年4月于加利福尼亚州洛杉矶举行的美国国际教育协会继续教育项目“改善艾滋病毒疾病管理”和2017年8月在德克萨斯州圣安东尼奥举行的2017年Ryan White艾滋病毒/艾滋病项目临床会议上的演讲。
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来源期刊
Topics in antiviral medicine
Topics in antiviral medicine Medicine-Pharmacology (medical)
CiteScore
1.80
自引率
0.00%
发文量
10
期刊最新文献
CROI 2024: Global Epidemiology and Prevention of HIV and Other Sexually Transmitted Diseases. CROI 2024: Metabolic and Other Complications of HIV Infection. CROI 2024: Summary of Basic Science Research in HIV. CROI 2024: Tuberculosis, Mpox, and Other Infectious Complications in People With HIV. Long-Term Effects of COVID-19: The Stories of 2 Physicians Who Became Patients.
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