Evidence map›Paper›PMID 28550352›Full record

Trial reportInternational journal of hematology2017

Efficacy and safety of full-length pegylated recombinant factor VIII with extended half-life in previously treated patients with hemophilia A: comparison of data between the general and Japanese study populations.

Keiji Nogami, Midori Shima, Katsuyuki Fukutake, Teruhisa Fujii, Masashi Taki, Tadashi Matsushita, Satoshi Higasa, Tetsuji Sato, Michio Sakai, Morio Arai and 4 more

Erratum issuedAbstract readClinical Trial, Phase IIClinical Trial, Phase IIIComparative Study
PubMed Publisher
In one paragraph

Trial report in International journal of hematology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 9 institutions in 2 countries.

Keiji NogamiDepartment of Pediatrics, Nara Medical University, Kashihara, Japan. roc-noga@naramed-u.ac.jp.
Midori ShimaDepartment of Pediatrics, Nara Medical University, Kashihara, Japan.
Katsuyuki FukutakeDepartment of Laboratory Medicine, Tokyo Medical University Hospital, Tokyo, Japan.
Teruhisa FujiiDepartment of Hematology and Oncology, Hiroshima University Hospital, Hiroshima, Japan.
Masashi TakiDepartment of Pediatrics, St. Marianna University School of Medicine, Kawasaki, Japan.
Tadashi MatsushitaDepartment of Transfusion Medicine, Nagoya University Hospital, Nagoya, Japan.
Satoshi HigasaDivision of Hematology, Hyogo College of Medicine Hospital, Nishinomiya, Japan.
Tetsuji SatoDepartment of Pediatrics, University of Occupational and Environmental Health, Kitakyushu, Japan.
Michio SakaiDepartment of Pediatrics, Munakata Suikokai General Hospital, Fukutsu, Japan.
Morio AraiDepartment of Medical Affairs, Baxalta Japan Ltd., Tokyo, Japan.
Haruhiko UchikawaDepartment of Clinical Development Operations, Baxalta Japan Ltd., Tokyo, Japan.
Werner EnglShire, Vienna, Austria.
Brigitt AbbuehlShire, Vienna, Austria.
Barbara A KonklePuget Sound Blood Center, University of Washington School of Medicine, Seattle, USA.
Nara Medical University · JPBloodworks Northwest · USHiroshima University Hospital · JPHyogo Medical University · JPNagoya University Hospital · JPSt. Marianna University School of Medicine · JPTokyo Medical University Hospital · JPUniversity of Occupational and Environmental Health Japan · JPYao Tokushukai General Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rurioctocog alfa pegol (BAX 855) is a novel third-generation recombinant factor VIII whose active ingredient is chemically modified with polyethylene glycol. A global multicenter phase 2/3 study of the product in 137 patients (including 11 patients from Japan) with severe hemophilia A aged 12-65 years, reported an extended half-life and a good tolerability profile, as well as a significantly lower annualized bleeding rate in the prophylactic treatment arm than in the on-demand treatment arm. Using descriptive statistics, a post hoc analysis was performed to compare the pharmacokinetics, safety, and efficacy profiles of the product in the Japanese subpopulation and the overall population. Extended half-life was demonstrated in the Japanese subpopulation. The mean [standard deviation (SD)] annualized bleeding rates in the prophylactic treatment arm were 3.7 (4.7) for the overall population (n = 120) and 4.0 (3.4) for the Japanese subpopulation (n = 11). The proportion of bleeds reported as excellent or good was 94.9% (149/157) in the overall population, whereas that in the Japanese subpopulation was 92.3% (12/13). No FVIII inhibition or anaphylactic reaction was reported in the Japanese subpopulation. The post hoc comparisons demonstrated similar pharmacokinetic, safety, and efficacy profiles between the overall population and the Japanese subpopulation.

Indexed as

AdolescentAdultAgedChildFactor VIIIFemaleHemophilia AHemorrhageHumansJapanMaleMiddle AgedBAX 855Factor VIIIAnnualized bleeding rateHemophilia APegylated full-length recombinant factor VIIIPhase 2/3 clinical studyPreviously treated patients

Identifiers

PMID28550352
OpenAlexW2617381198

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.