Evidence map›Paper›PMID 28559255›Full record

Trial reportAntimicrobial agents and chemotherapy2017

A Phase 1, Randomized, Double-Blind, Placebo-Controlled, Single-Ascending-Dose Study To Investigate the Safety, Tolerability, and Pharmacokinetics of an Anti-Influenza B Virus Monoclonal Antibody, MHAB5553A, in Healthy Volunteers.

Jeremy J Lim, Michael A Derby, Yaping Zhang, Rong Deng, Richard Larouche, Malia Anderson, Mauricio Maia, Stéphanie Carrier, Isabelle Pelletier, Johanne Girard and 3 more

Registry-linked trialAbstract readClinical Trial, Phase IRandomized Controlled Trial
In one paragraph

Trial report in Antimicrobial agents and chemotherapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02528903 (A Phase 1, Randomized, Double-blind, Placebo-controlled, Single-ascending Dose Study to Investigate the Safety, Tolerability, and Pharmacokinetics of MHAB5553A in Healthy Volunteers), which is not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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.

NCT02528903 phase1completednot on this map

A Phase 1, Randomized, Double-blind, Placebo-controlled, Single-ascending Dose Study to Investigate the Safety, Tolerability, and Pharmacokinetics of MHAB5553A in Healthy Volunteers

TypeinterventionalSponsorGenentech, Inc.Ran2015 to 2016Enrolled26ConditionsHealthy VolunteerArmsMHAB5553A, Matching placebo
3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
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

13 authors.

Jeremy J LimGenentech, Inc., South San Francisco, California, USA lim.jeremy@gene.com.
Michael A DerbyGenentech, Inc., South San Francisco, California, USA.
Yaping ZhangGenentech, Inc., South San Francisco, California, USA.
Rong DengGenentech, Inc., South San Francisco, California, USA.
Richard LaroucheinVentiv Health Clinical, Québec, Canada.
Malia AndersonGenentech, Inc., South San Francisco, California, USA.
Mauricio MaiaGenentech, Inc., South San Francisco, California, USA.
Stéphanie CarrierinVentiv Health Clinical, Québec, Canada.
Isabelle PelletierinVentiv Health Clinical, Québec, Canada.
Johanne GirardinVentiv Health Clinical, Québec, Canada.
Priya KulkarniGenentech, Inc., South San Francisco, California, USA.
Elizabeth NewtonGenentech, Inc., South San Francisco, California, USA.
Jorge A TavelGenentech, Inc., South San Francisco, California, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Influenza B can cause significant morbidity and mortality. MHAB5553A, a human monoclonal immunoglobulin G1 (IgG1) antibody that binds to a highly conserved region of the hemagglutinin protein of influenza B virus, is being examined as a novel therapeutic for the treatment of influenza B patients with severe disease. This phase 1, randomized, double-blind, placebo-controlled, single-ascending-dose study was conducted to assess the safety, tolerability, and pharmacokinetics (PK) of MHAB5553A. Twenty-six healthy male and female volunteers of >18 years of age were randomized into five cohorts receiving a single intravenous (i.v.) dose of 120, 1,200, 3,600, 8,400, or 10,800 mg MHAB5553A or placebo (four active:one placebo, except for the 120-mg cohort [4:2]). Subjects were followed for 120 days after dosing. No subject discontinued the study, no dose-limiting adverse events or serious adverse events were reported, and a maximum tolerated dose (MTD) was not defined. The most commonly reported adverse events were cold symptoms and headache; most were mild and occurred at a similar rate across all cohorts. MHAB5553A showed no relevant time- or dose-related changes in laboratory values or vital signs compared to the placebo. The observed serum PK was linear and generally dose proportional, and the observed nasal PK was nonlinear and generally non-dose proportional. MHAB5553A is generally well tolerated in healthy volunteers up to at least a single i.v. dose of 10,800 mg and demonstrated linear serum PK consistent with those of a human IgG1 antibody lacking known endogenous targets in humans. (This study has been registered at ClinicalTrials.gov under registration no. NCT02528903.).

Indexed as

AdultAntibodies, Monoclonal, HumanizedAntibodies, ViralAntiviral AgentsDose-Response Relationship, DrugDouble-Blind MethodFemaleHemagglutinins, ViralHumansImmunoglobulin GInfluenza B virusInfluenza, HumanMaleMiddle AgedPlacebosAntibodies, Monoclonal, HumanizedAntibodies, ViralAntiviral AgentsHemagglutinins, ViralImmunoglobulin GlesofavumabPlacebosantiviral agentsinfluenza BMHAB5553Amonoclonal antibodies

Identifiers

PMID28559255
PMCPMC5527589

What OpenQuestion holds

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Registered trials

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.