Evidence map›Paper›PMID 26097793›Full record

ArticleClinical pharmacology in drug development2015

Intravenous Pharmacokinetics, Local Tolerability, and Hemolysis of an SBE7-β-Cyclodextrin Formulation of the Neurokinin-1 Receptor Antagonist Vestipitant.

Richard A Brigandi, Steven F Russ, Chantal Petit, Brendan Johnson, Scott Croy, Peter Hodsman, Fran Muller

Open access · hybridAbstract read
In one paragraph

Article in Clinical pharmacology in drug development, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 31% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. 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

7 authors at 4 institutions in 4 countries.

Richard A BrigandiVirtual Proof of Concept Discovery Performance Unit (VPoC DPU), GlaxoSmithKline King of Prussia, PA, USA.
Steven F RussVPoC DPU, GlaxoSmithKline Research Triangle Park, NC, USA.
Chantal PetitVirtual Proof of Concept Discovery Performance Unit (VPoC DPU), GlaxoSmithKline King of Prussia, PA, USA.
Brendan JohnsonClinical Pharmacology Modeling and Simulation, GlaxoSmithKline Research Triangle Park, NC, USA.
Scott CroyGlobal Formulation Development, GlaxoSmithKline Collegville, PA, USA.
Peter HodsmanFormerly of Nucleus Network Melbourne, Victoria, Australia.
Fran MullerGlobal Formulation Development, GlaxoSmithKline Collegville, PA, USA.
GlaxoSmithKline (United Kingdom) · GBGlaxoSmithKline (United States) · USResearch Triangle Park Foundation · USBreast Cancer Network Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vestipitant is a potent and selective neurokinin 1 (NK-1) receptor antagonist that was investigated as a potential treatment for post-operative nausea and vomiting (PONV). A previous mannitol-based formulation of vestipitant was associated with hemolytic activity in preclinical studies. In an effort to reduce the hemolytic potential and develop an IV formulation of vestipitant that could be administered more rapidly, an IV formulation containing sulfobutylether-7-beta-cyclodextrin (SBE7-β-CD, Captisol™) was developed and tested in a phase 1 clinical study. This was a randomized, single-blind (subjects and investigator-blinded, sponsor-unblinded), placebo controlled, dose escalation study in healthy subjects in which 7 cohorts of 8 subjects per cohort received SBE7-β-CD -based vestipitant (2 mg/mL) or placebo (saline) in a 3:1 ratio (active:placebo) at different doses and infusion rates. The results demonstrated the ability to infuse up to 48 mg vestipitant in a 2 mg/mL formulation over 30 seconds with no evidence of hemolytic effects. Cohorts of subjects at lower doses and longer infusion duration (>1 minute) reported more AEs related to the infusion site than those at the higher doses and faster infusion rates.

Indexed as

hemolysisintravenousNK-1 receptor antagonistSBE7-β-cyclodextrinvestipitant

Identifiers

PMID26097793
PMCPMC4467239
OpenAlexW1535931706

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.