Evidence map›Paper›PMID 34133466›Full record

ArticlePloS one2021

Physicochemical and functional characterization of MYL-1501D, a proposed biosimilar to insulin glargine.

Parag Goyal, Harish Venkatraman Pai, Phanichand Kodali, Bhavesh Vats, Navratna Vajpai, Shankara Annegowda, Krishnappa Mane, Shamini Mohan, Shruti Saxena, Anil Bangalore Veerabhadraia and 15 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

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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

25 authors at 2 institutions in 2 countries.

Parag GoyalViatris Inc, Canonsburg, PA, United States of America.ORCID 0000-0002-5678-8592
Harish Venkatraman PaiBiocon Research Limited, Bangalore, India.
Phanichand KodaliBiocon Research Limited, Bangalore, India.
Bhavesh VatsViatris Inc, Hyderabad, India.
Navratna VajpaiBiocon Research Limited, Bangalore, India.
Shankara AnnegowdaBiocon Research Limited, Bangalore, India.
Krishnappa ManeBiocon Research Limited, Bangalore, India.
Shamini MohanBiocon Research Limited, Bangalore, India.
Shruti SaxenaBiocon Research Limited, Bangalore, India.
Anil Bangalore VeerabhadraiaBiocon Research Limited, Bangalore, India.
Milee PalandeBiocon Research Limited, Bangalore, India.
Preethy Sasankan NairBiocon Research Limited, Bangalore, India.
Digvijay Chandrashekar MoreBiocon Research Limited, Bangalore, India.
Umamaheshwara Rao KarudumpaBiocon Research Limited, Bangalore, India.
Kunala JyothirmaiBiocon Research Limited, Bangalore, India.
Adroha BhattacharyaBiocon Research Limited, Bangalore, India.
Frida AlmeidaBiocon Research Limited, Bangalore, India.
Santosh Gulab KhyadeBiocon Research Limited, Bangalore, India.
Shankara GoudaViatris Inc, Hyderabad, India.
Daniel J RanayhossainiViatris Inc, Canonsburg, PA, United States of America.
Praveen Reddy MooleBiocon Research Limited, Bangalore, India.
Jeffrey P SmithViatris Inc, Canonsburg, PA, United States of America.
Abhijit BarveViatris Inc, Canonsburg, PA, United States of America.
Ramakrishnan MelarkodeBiocon Research Limited, Bangalore, India.
Rajesh UllanatViatris Inc, Hyderabad, India.
Biocon (India) · INCanon (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Insulin glargine is a long-acting analogue of human insulin that has been used to manage hyperglycemia in patients with diabetes mellitus (DM) for nearly 20 years. Insulin glargine has a relatively constant concentration-time profile that mimics basal levels of insulin and allows for once-daily administration. MYL-1501D is a biosimilar insulin glargine designed to offer greater access of insulin glargine to patients, with comparable efficacy and safety to the marketed reference product. We conducted a comprehensive panel of studies based on a formal analysis of critical quality attributes to characterize the structural and functional properties of MYL-1501D and reference insulin glargine products available in the United States and European Union. MYL-1501D was comprehensively shown to have high similarity to the reference products in terms of protein structure, metabolic activity (both in vitro cell-based assays and in vivo rabbit bioassays), and in vitro cell-based assays for mitogenic activity. The structural analyses demonstrated that the primary protein sequence was identical, and secondary and tertiary structures are similar between the proposed biosimilar and the reference products. Insulin receptor binding affinity and phosphorylation studies also established analytical similarity. MYL-1501D demonstrated high similarity in different metabolic assays of glucose uptake, adipogenesis activity, and inhibition of stimulated lipolysis. Rabbit bioassay studies showed MYL-1501D and EU-approved insulin glargine are highly similar to US-licensed insulin glargine. These product quality studies show high similarity between MYL-1501D and licensed or approved insulin glargine products and suggest the potential of MYL-1501D as an alternative cost-effective treatment option for patients and clinicians.

Indexed as

3T3 CellsAdipogenesisAmino Acid SequenceAnimalsBiosimilar PharmaceuticalsCHO CellsCircular DichroismCricetulusGas Chromatography-Mass SpectrometryGlucoseHumansInsulin GlargineLipolysisMagnetic Resonance SpectroscopyMiceProtein Structure, SecondaryBiosimilar PharmaceuticalsGlucoseInsulin GlargineMYL-1501D

Identifiers

PMID34133466
PMCPMC8208551
OpenAlexW3171066078

What OpenQuestion holds

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Registered trials

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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.