Evidence map›Paper›PMID 32172488›Full record

Trial reportEuropean journal of drug metabolism and pharmacokinetics2020

An Open-Label, Randomized, Single-Dose, Crossover, Comparative Pharmacokinetics Study of YLB113 and the Etanercept Reference Product in Healthy Adult Male Subjects.

Mustafa Shennak, Rana Al-Jaouni, Santhosh Kshirasagar, Ravi Sekhar Kasibhatta, Neelima Godse, Ahmad Al-Ghazawi, Praveen Vittala, Dhananjay Bakhle

Open access · hybridAbstract readComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in European journal of drug metabolism and pharmacokinetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 36% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. 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

8 authors at 2 institutions in 2 countries.

Mustafa ShennakTriumpharma, 07 Yaroot St, Opposite Jubaiya Circle, Amman, 00962, Jordan. PI@triumpharma.com.ORCID http://orcid.org/0000-0002-3508-9522
Rana Al-JaouniTriumpharma, 07 Yaroot St, Opposite Jubaiya Circle, Amman, 00962, Jordan.
Santhosh KshirasagarLupin Limited, Mumbai, India.
Ravi Sekhar KasibhattaLupin Limited, Mumbai, India.
Neelima GodseLupin Limited, Mumbai, India.
Ahmad Al-GhazawiTriumpharma, 07 Yaroot St, Opposite Jubaiya Circle, Amman, 00962, Jordan.
Praveen VittalaLupin Limited, Mumbai, India.
Dhananjay BakhleLupin Limited, Mumbai, India.
Lupin Pharmaceuticals (India) · INTrillium Therapeutics (Canada) · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesYLB113 is being developed as a biosimilar of the antitumor necrosis factor-alpha antagonist etanercept, which is approved for the treatment of moderate-to-severe rheumatoid arthritis (RA) and other chronic immune-mediated inflammatory diseases. An open-label, crossover, pharmacokinetic study was conducted to compare the relative bioavailability and safety of YLB113 and the etanercept reference product (RP) Enbrel

methodsHealthy male subjects aged 18-50 years were randomized to receive a single subcutaneous dose of YLB113 in one period and the etanercept RP in another period. A washout period of 28 days separated the two treatment periods. Blood samples were collected for pharmacokinetic analysis predose and until 480 h postdose during both periods.

resultsOverall, 52 subjects were enrolled, including 51 subjects who completed the first period and 43 subjects who completed the second period. The 90% confidence intervals for the least squares means derived from an analysis of the log-transformed pharmacokinetic parameters maximum serum concentration (C

conclusionsA single dose of YLB113 exhibited pharmacokinetic and safety profiles comparable with those of the etanercept RP in healthy adult male subjects. Therefore, YLB113 and the etanercept RP can be considered bioequivalent. These findings support the continued development of YLB113 for use in patients with RA. JORDAN FOOD & DRUG ADMINISTRATION UNIQUE TRIAL NUMBER: 31/Clinical/2018.

Indexed as

AdultBiological AvailabilityBiosimilar PharmaceuticalsCross-Over StudiesDrug MonitoringEtanerceptHealthy VolunteersHumansInjections, SubcutaneousJordanMaleMiddle AgedTherapeutic EquivalencyTumor Necrosis Factor InhibitorsYoung AdultBiosimilar PharmaceuticalsEtanerceptTumor Necrosis Factor Inhibitors

Identifiers

PMID32172488
PMCPMC7359121
OpenAlexW3010713619

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.