Evidence map›Paper›PMID 30460996›Full record

Trial reportClinical pharmacology and therapeutics2019

Bioequivalence and Therapeutic Equivalence of Generic and Brand Bupropion in Adults With Major Depression: A Randomized Clinical Trial.

Evan D Kharasch, Alicia Neiner, Kristin Kraus, Jane Blood, Angela Stevens, Julia Schweiger, J Philip Miller, Eric J Lenze

Registry-linked trialOpen access · greenAbstract readComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in Clinical pharmacology and therapeutics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05216614 (Fluvoxamine to Augment Olfactory Recovery For Long COVID-19 Parosmia), which is not on this map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 23% 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.

NCT05216614 phase2withdrawnnot on this mapstarted 2021, after this paper: background citation

Fluvoxamine to Augment Olfactory Recovery For Long COVID-19 Parosmia (FluCOP Trial)

TypeinterventionalSponsorWashington University School of MedicineRan2021 to 2022Enrolled0ConditionsCOVID-19, Olfactory Disorder, ParosmiaArmsFluvoxamine, Placebo
3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Pharmacogenetic Influence on Stereoselective Steady-State Disposition of Bupropion.Drug metabolism and disposition: the biological fate of chemicals · 2024
    Trial
  2. Trial
  3. Article
  4. Review
  5. Article
  6. Impact and implications of national centralized drug procurement in China.International journal of clinical pharmacy · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. 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

8 authors at 2 institutions in 1 country.

Evan D KharaschDepartment of Anesthesiology, Duke University School of Medicine, Durham, North Carolina, USA.
Alicia NeinerDepartment of Anesthesiology, Washington University in St. Louis, St. Louis, Missouri, USA.
Kristin KrausDepartment of Anesthesiology, Washington University in St. Louis, St. Louis, Missouri, USA.
Jane BloodDepartment of Anesthesiology, Washington University in St. Louis, St. Louis, Missouri, USA.
Angela StevensDepartment of Psychiatry, Washington University in St. Louis, St. Louis, Missouri, USA.
Julia SchweigerDepartment of Psychiatry, Washington University in St. Louis, St. Louis, Missouri, USA.
J Philip MillerDivision of Biostatistics, Washington University in St. Louis, St. Louis, Missouri, USA.
Eric J LenzeDepartment of Psychiatry, Washington University in St. Louis, St. Louis, Missouri, USA.
Washington University in St. Louis · USDuke University · US

Funding

BIOEQUIVALENCE AND CLINICAL IMPLICATIONS OF GENERIC BUPROPIONU01FD004899 · FDA · WASHINGTON UNIVERSITY · PI KHARASCH, EVAN D. · 2013 to 2015
$2.8M
FDA HHS U01 FD004899
6 · The paper itself

Abstract

Controversy persists about bupropion XL 300 mg generic equivalence to brand product. A prospective, randomized, double-blinded crossover in 70 adults with major depression in stable remission taking any bupropion XL 300 mg tested bioequivalence and therapeutic equivalence of available XL 300 mg products. After a 4-week lead-in on patients' existing bupropion, four 6-week phases evaluated brand and three generics. Patients were uninformed of switching. Drug overencapsulation ensured blinding. There were no differences between any generic and brand, or between generics, in peak plasma concentration (C

Indexed as

AdultAntidepressive Agents, Second-GenerationBupropionCross-Over StudiesDouble-Blind MethodDrugs, GenericFemaleHumansMajor Depressive DisorderMaleMiddle AgedProspective StudiesTherapeutic EquivalencyTreatment OutcomeAntidepressive Agents, Second-GenerationBupropionDrugs, Generic

Identifiers

PMID30460996
PMCPMC6465131
OpenAlexW2901045961

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.