Evidence map›Paper›PMID 32621543›Full record

Trial reportJournal of clinical pharmacology2020

Pharmacokinetics of the Monoclonal Antibody MHAA4549A Administered in Combination With Oseltamivir in Patients Hospitalized With Severe Influenza A Infection.

Rong Deng, Gaohong She, Mauricio Maia, Jeremy J Lim, Melicent C Peck, Jacqueline M McBride, Priya Kulkarni, Priscilla Horn, Aide Castro, Elizabeth Newton and 2 more

Open access · bronzeAbstract readClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in Journal of clinical pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Trial
  2. Article
  3. Monoclonal Antibodies and Hyperimmune Immunoglobulins in the Next Pandemic.Current topics in microbiology and immunology · 2025
    Review
  4. Article
  5. Drug Cocktail Formulation via Circuit Design.IEEE transactions on molecular, biological, and multi-scale communications · 2023
    Article
  6. Review
  7. Article
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

12 authors at 2 institutions in 1 country.

Rong DengGenentech, Inc, South San Francisco, California, USA.
Gaohong SheGenentech, Inc, South San Francisco, California, USA.
Mauricio MaiaGenentech, Inc, South San Francisco, California, USA.
Jeremy J LimGenentech, Inc, South San Francisco, California, USA.
Melicent C PeckGenentech, Inc, South San Francisco, California, USA.
Jacqueline M McBrideGenentech, Inc, South San Francisco, California, USA.
Priya KulkarniGenentech, Inc, South San Francisco, California, USA.
Priscilla HornGenentech, Inc, South San Francisco, California, USA.
Aide CastroGenentech, Inc, South San Francisco, California, USA.
Elizabeth NewtonGenentech, Inc, South San Francisco, California, USA.
Jorge A TavelGenentech, Inc, South San Francisco, California, USA.
William D HanleyGenentech, Inc, South San Francisco, California, USA.
Enzo Life Sciences (United States) · USSeagen (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MHAA4549A is a human anti-influenza A monoclonal antibody developed to treat influenza A. We report MHAA4549A serum, nasopharyngeal, and tracheal aspirate pharmacokinetics from a phase 2b study in hospitalized patients with severe influenza A. Patients were randomized 1:1:1 into 3 groups receiving single intravenous doses of 3600 mg (n = 55) or 8400 mg (n = 47) MHAA4549A or placebo (n = 56). Patients also received oral oseltamivir twice daily for ≥5 days. Serum, nasopharyngeal, and tracheal aspirate pharmacokinetic samples were collected on days 1-60 from MHAA4549A-treated groups. Day 5 plasma samples from all groups were collected for assessing the pharmacokinetics of oseltamivir and its active metabolite, oseltamivir carboxylate. Noncompartmental pharmacokinetic analysis was performed using Phoenix WinNonlin. Data were collected during a preplanned interim analysis that became final when the trial terminated because of a lack of efficacy. Serum MHAA4549A concentrations were dose-proportional and biphasic. Mean MHAA4549A clearance was 288-350 mL/day, and mean half-life was 17.8-19.0 days. Nasopharyngeal MHAA4549A concentrations were non-dose-proportional. We detected MHAA4549A in tracheal aspirate samples, but intersubject variability was high. MHAA4549A serum and nasopharyngeal exposures were confirmed in all MHAA4549A-treated patients. Serum MHAA4549A had faster clearance and a shorter half-life in influenza A-infected patients compared with healthy subjects. MHAA4549A detection in tracheal aspirate samples indicated exposure in the lower respiratory tract. Oseltamivir and oseltamivir carboxylate exposures were similar between MHAA4549A-treated and placebo groups, suggesting a lack of MHAA4549A interference with oseltamivir pharmacokinetics.

Indexed as

Administration, OralAgedAntibodies, Monoclonal, HumanizedAntibodies, NeutralizingAntiviral AgentsDrug Therapy, CombinationHalf-LifeHumansInfluenza A virusInfluenza, HumanInfusions, IntravenousInpatientsMiddle AgedNasopharynxOseltamivirTracheaAntibodies, Monoclonal, HumanizedAntibodies, NeutralizingAntiviral AgentsgedivumabOseltamiviroseltamivir carboxylateantiviral agentsinfluenza A virusMHAA4549Amonoclonal antibodypharmacokinetics and drug metabolism

Identifiers

PMID32621543
PMCPMC7586956
OpenAlexW3038845910

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.