Evidence map›Paper›PMID 32302352›Full record

ArticlePloS one2020

Physicochemical and biological evaluation of JR-131 as a biosimilar to a long-acting erythropoiesis-stimulating agent darbepoetin alfa.

Junya Tani, Yae Ito, Satoshi Tatemichi, Makoto Yamakami, Tsuyoshi Fukui, Yukichi Hatano, Shinji Kakimoto, Ayaka Kotani, Atsushi Sugimura, Kazutoshi Mihara and 5 more

Open access · goldAbstract readEvaluation Study
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. 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

15 authors at 2 institutions in 1 country.

Junya TaniResearch Division, JCR Pharmaceuticals Co., Ltd., Kobe, Japan.
Yae ItoResearch Division, JCR Pharmaceuticals Co., Ltd., Kobe, Japan.
Satoshi TatemichiResearch Division, Kissei Pharmaceutical Co., Ltd., Azumino, Japan.
Makoto YamakamiResearch Division, JCR Pharmaceuticals Co., Ltd., Kobe, Japan.
Tsuyoshi FukuiResearch Division, JCR Pharmaceuticals Co., Ltd., Kobe, Japan.
Yukichi HatanoResearch Division, JCR Pharmaceuticals Co., Ltd., Kobe, Japan.
Shinji KakimotoResearch Planning Division, JCR Pharmaceuticals Co., Ltd., Kobe, Japan.
Ayaka KotaniResearch Planning Division, JCR Pharmaceuticals Co., Ltd., Kobe, Japan.
Atsushi SugimuraResearch Division, JCR Pharmaceuticals Co., Ltd., Kobe, Japan.
Kazutoshi MiharaResearch Division, JCR Pharmaceuticals Co., Ltd., Kobe, Japan.
Ryuji YamamotoResearch Division, JCR Pharmaceuticals Co., Ltd., Kobe, Japan.
Noboru TanakaResearch Division, JCR Pharmaceuticals Co., Ltd., Kobe, Japan.
Kohtaro MinamiResearch Division, JCR Pharmaceuticals Co., Ltd., Kobe, Japan.ORCID 0000-0003-4698-6250
Kenichi TakahashiResearch Division, JCR Pharmaceuticals Co., Ltd., Kobe, Japan.
Tohru HiratoResearch Division, JCR Pharmaceuticals Co., Ltd., Kobe, Japan.
JCR Pharmaceuticals (Japan) · JPKissei Pharmaceutical (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Renal anemia is predominantly caused by a relative deficiency in erythropoietin (EPO). Conventional treatment for renal anemia includes the use of recombinant human EPO (rhEPO) or a long-acting erythropoiesis-activating agent named darbepoetin alfa, which is a modified rhEPO with a carbohydrate chain structure that differs from native hEPO. We have developed a biosimilar to darbepoetin alfa designated JR-131. Here, we comprehensively compare the physicochemical and biological characteristics of JR-131 to darbepoetin alfa. JR-131 demonstrated similar protein structure to the originator, darbepoetin alfa, by peptide mapping and circular dichroism spectroscopy. Additionally, mass spectroscopic analyses and capillary zone electrophoresis revealed similar glycosylation patterns between the two products. Human bone marrow-derived erythroblasts differentiated and proliferated to form colonies with JR-131 to a similar degree as darbepoetin alfa. Finally, JR-131 stimulated erythropoiesis and improved anemia in rats similarly to darbepoetin alfa. Our data show the similarity in physicochemical and biological properties of JR-131 to those of darbepoetin alfa, and JR-131 therefore represents a biosimilar for use in the treatment of renal anemia.

Indexed as

AnemiaAnimalsBiosimilar PharmaceuticalsCHO CellsCricetinaeCricetulusDarbepoetin alfaDisease Models, AnimalElectrophoresis, CapillaryErythropoiesisGlycosylationKidneyMaleMolecular WeightNephrectomyPeptide MappingBiosimilar PharmaceuticalsDarbepoetin alfaSugars

Identifiers

PMID32302352
PMCPMC7164597
OpenAlexW3017080205

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.