Phase I evaluation of the safety, tolerability, and pharmacokinetics of GSK3640254, a next‐generation HIV‐1 maturation inhibitor

Author:

Joshi Samit R.1ORCID,Fernando Disala2,Igwe Stephanie2,McKenzie Litza3,Krishnatry Anu S.4,Halliday Fiona5,Zhan Joyce4,Greene Thomas J.4,Xu Jianfeng4,Ferron‐Brady Geraldine4,Lataillade Max1,Min Sherene6

Affiliation:

1. ViiV Healthcare Branford CT USA

2. GlaxoSmithKline Clinical Unit Cambridge Cambridge UK

3. Quotient Sciences Nottingham UK

4. GlaxoSmithKline Upper Providence PA USA

5. GlaxoSmithKline Stockley Park UK

6. ViiV Healthcare Research Triangle Park NC USA

Funder

ViiV Healthcare

Publisher

Wiley

Subject

General Pharmacology, Toxicology and Pharmaceutics,Neurology

Reference7 articles.

1. Virus maturation as a new HIV-1 therapeutic target

2. DeJesusE HarwardS JewellRC et al.A phase IIa study of novel maturation inhibitor GSK2838232 in HIV patients. Slides presented at: Conference on Retroviruses and Opportunistic Infections; March 4–7 2019; Seattle WA.

3. Safety, efficacy, and dose response of the maturation inhibitor GSK3532795 (formerly known as BMS‐955176) plus tenofovir/emtricitabine once daily in treatment‐naive HIV‐1‐infected adults: week 24 primary analysis from a randomized phase IIb trial;Morales‐Ramirez J;PLoS One,2018

4. Can the further clinical development of bevirimat be justified?;Wainberg MA;AIDS,2010

5. Pharmacological intervention of HIV-1 maturation

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