Evidence map›Paper›PMID 30885900›Full record

ReviewAntimicrobial agents and chemotherapy2019

Ibalizumab, a Novel Monoclonal Antibody for the Management of Multidrug-Resistant HIV-1 Infection.

Mario V Beccari, Bryan T Mogle, Eric F Sidman, Keri A Mastro, Elizabeth Asiago-Reddy, Wesley D Kufel

Open access · bronzeAbstract readReview
In one paragraph

Review in Antimicrobial agents and chemotherapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
6.4field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 95 citations in OpenAlex.

  1. Pooled it
  2. Article
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  12. Article
  13. A Narrative Review of Novel Agents for Managing Heavily Treatment-Experienced People Living With HIV.The Journal of pharmacy technology : jPT : official publication of the Association of Pharmacy Technicians · 2024
    Review
  14. Review
  15. Review
  16. Review
  17. Navigating the Nexus: HIV and Breast Cancer-A Critical Review.International journal of molecular sciences · 2024
    Review
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  19. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Mario V BeccariState University of New York Upstate University Hospital, Syracuse, New York, USA.
Bryan T MogleState University of New York Upstate University Hospital, Syracuse, New York, USA.ORCID 0000-0003-2993-6366
Eric F SidmanState University of New York Upstate University Hospital, Syracuse, New York, USA.
Keri A MastroBinghamton University School of Pharmacy and Pharmaceutical Sciences, Binghamton, New York, USA.
Elizabeth Asiago-ReddyState University of New York Upstate Medical University, Syracuse, New York, USA.
Wesley D KufelState University of New York Upstate University Hospital, Syracuse, New York, USA wkufel@binghamton.edu.ORCID 0000-0001-7703-096X
State University of New York · USBinghamton University · USSUNY Upstate Medical University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Limited antiretrovirals are currently available for the management of multidrug-resistant (MDR) HIV-1 infection. Ibalizumab, a recombinant humanized monoclonal antibody, represents the first novel agent for HIV-1 management in over a decade and is the first monoclonal antibody for the treatment of MDR HIV-1 infection in combination with other forms of antiretroviral therapy in heavily treatment-experienced adults who are failing their current antiretroviral regimen. Ibalizumab demonstrates a novel mechanism of action as a CD4-directed postattachment inhibitor and has a favorable pharmacokinetic profile that allows for a dosing interval of every 14 days after an initial loading dose. Clinical studies have demonstrated reasonably substantial antiretroviral activity with ibalizumab among a complex patient population with advanced HIV-1 infection who are receiving an optimized background regimen, where limited therapeutic options exist. Ibalizumab was well tolerated in clinical trials, and the most common adverse effects included diarrhea, nausea, dizziness, fatigue, pyrexia, and rash. Resistance to ibalizumab has also been observed via reduced expression or loss of the potential N-linked glycosylation sites in the V5 loop of the envelope glycoprotein 120. The mechanism of action, pharmacokinetic parameters, efficacy, and safety of ibalizumab present an advance in the management of MDR HIV-1 infection. Future studies and postmarketing experience will further determine longer-term clinical efficacy, safety, and resistance data for ibalizumab.

Indexed as

Antibodies, MonoclonalAnti-HIV AgentsCD4 AntigensCD4-Positive T-LymphocytesDrug Resistance, ViralHIV-1HIV InfectionsHumansAntibodies, MonoclonalAnti-HIV AgentsCD4 AntigensibalizumabantiretroviralCD4 postattachment inhibitorHIVibalizumabibalizumab-uiykmonoclonal antibodymultidrug-resistant HIV

Identifiers

PMID30885900
PMCPMC6535568
OpenAlexW2921797648

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.