Evidence map›Paper›PMID 35420397›Full record

ArticleDiabetes therapy : research, treatment and education of diabetes and related disorders2022

Biosimilar Insulin Aspart Premix SAR341402 Mix 70/30 Versus Originator Insulin Aspart Mix 70/30 (NovoMix 30) in People with Diabetes: A 26-Week, Randomized, Open-Label Trial (GEMELLI M).

S R Aravind, Kiran P Singh, Grace Aquitania, Liliia Mogylnytska, Alsu G Zalevskaya, Beata Matyjaszek-Matuszek, Karin Wernicke-Panten, My-Liên Nguyên-Pascal, Suzanne Pierre, Baerbel Rotthaeuser and 2 more

Abstract read
In one paragraph

Article in Diabetes therapy : research, treatment and education of diabetes and related disorders, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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.

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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. 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.

S R AravindDiabetes Care and Research Center, Diacon Hospital, Bangalore, India.
Kiran P SinghDepartment of Endocrinology, Fortis Hospital Mohali, Chandigarh, India.
Grace AquitaniaDavao Doctors Hospital, Davao City, Philippines.
Liliia MogylnytskaKhmelnytskyi Regional Hospital, Khmelnytskyi, Ukraine.
Alsu G ZalevskayaDepartment of Endocrinology, First Pavlov State Medical University, St. Petersburg, Russia.
Beata Matyjaszek-MatuszekDepartment of Endocrinology, Medical University of Lublin, Lublin, Poland.
Karin Wernicke-PantenSanofi-Aventis Deutschland GmbH, Frankfurt, Germany.
My-Liên Nguyên-PascalSanofi-Aventis Research and Development, Chilly-Mazarin, France.
Suzanne PierreSanofi-Aventis Research and Development, Chilly-Mazarin, France.
Baerbel RotthaeuserSanofi-Aventis Deutschland GmbH, Frankfurt, Germany.
Daniel KramerSanofi-Aventis Deutschland GmbH, Frankfurt, Germany.
Bhaswati MukherjeeSanofi, 54 Rue La Boétie, 75008, Paris, France. Bhaswati.Mukherjee@sanofi.com.ORCID http://orcid.org/0000-0002-7465-9225

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThis study compared the efficacy, safety, and immunogenicity of biosimilar insulin aspart premix SAR341402 Mix 70/30 (SAR

methodsThis 26-week, open-label, phase 3 trial enrolled 402 people with T1D (n = 105) or T2D (n = 297) previously treated with premix insulin, who were randomized (1:1) to SAR

resultsAfter 26 weeks, the least squares (LS) mean [median] change in HbA1c from baseline was similar in both treatment groups (SAR

conclusionsThe totality of evidence indicates that SAR

trial registrationEudraCT number 2017-000092-84.

Indexed as

BiosimilarGEMELLI MInsulin aspart mixPremixSAR341402

Identifiers

PMID35420397
PMCPMC9008602

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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.