Evidence map›Paper›PMID 28781129›Full record

Trial reportEBioMedicine2017

Safety, Tolerability and Pharmacokinetics of Single Doses of Oxytocin Administered via an Inhaled Route in Healthy Females: Randomized, Single-blind, Phase 1 Study.

Disala Fernando, Sarah Siederer, Sunita Singh, Ian Schneider, Ashutosh Gupta, Marcy Powell, Duncan Richards, Michelle P McIntosh, Peter Lambert, Susan Fowles

Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase IComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in EBioMedicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02542813 (A Single Centre, Single Blind Study to Investigate the Safety, Tolerability and Pharmacokinetics of Single Doses of Oxytocin), which is not on this map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.5field-weighted citation impact, top 11% 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.

NCT02542813 phase1completednot on this map

A Single Centre, Single Blind Study to Investigate the Safety, Tolerability and Pharmacokinetics of Single Doses of Oxytocin (GR121619) Administered Via an Inhaled Route in Healthy Female Volunteers

TypeinterventionalSponsorGlaxoSmithKlineRan2015 to 2015Enrolled16ConditionsPostpartum HemorrhageArmsIM oxytocin 10 IU, IH oxytocin 50 mcg, IH oxytocin 200 mcg, IH oxytocin 400 mcg, IH oxytocin 600 mcg
3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 28 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Review
  5. Review
  6. Innovations in the prevention and treatment of postpartum hemorrhage: Analysis of a novel medicines development pipeline database.International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics · 2022
    Article
  7. Article
  8. Article
  9. Article
  10. 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

10 authors at 6 institutions in 3 countries.

Disala FernandoGSK Clinical Unit Cambridge, Addenbrooke's Hospital NHS Trust, Cambridge, UK. Electronic address: disala.x.fernando@gsk.com.
Sarah SiedererClinical Pharmacology Modelling and Simulation Department, GSK, Stevenage, Herts, UK. Electronic address: Sarah.K.Siederer@gsk.com.
Sunita SinghClinical Operations, GSK, Stevenage, Herts, UK. Electronic address: sunita.p.singh@gsk.com.
Ian SchneiderGSK Clinical Unit Cambridge, Addenbrooke's Hospital NHS Trust, Cambridge, UK. Electronic address: ian.j.schneider@gsk.com.
Ashutosh GuptaQuantitative Sciences India, GSK, Bangalore, India. Electronic address: drashutoshgupta@outlook.com.
Marcy PowellClinical Safety, GSK, Research Triangle Park, NC, USA. Electronic address: marcy.x.powell@gsk.com.
Duncan RichardsAlternative Discovery and Development, GSK, Stevenage, Herts, UK. Electronic address: Duncan.B.Richards@gsk.com.
Michelle P McIntoshDrug Delivery, Disposition and Dynamics, Monash Institute of Pharmaceutical Sciences, Monash University, Melbourne, Australia. Electronic address: michelle.mcintosh@monash.edu.
Peter LambertDrug Delivery, Disposition and Dynamics, Monash Institute of Pharmaceutical Sciences, Monash University, Melbourne, Australia. Electronic address: pete.lambert@monash.edu.
Susan FowlesAlternative Discovery and Development, GSK, Stevenage, Herts, UK.
Age UK · GBMonash University · AUAddenbrooke's Hospital · GBCambridge University Hospitals NHS Foundation Trust · GBResearch Triangle Park Foundation · USThe Dialogue · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe utility of intramuscular (IM) oxytocin for the prevention of postpartum hemorrhage in resource-poor settings is limited by the requirement for temperature-controlled storage and skilled staff to administer the injection. We evaluated the safety, tolerability and pharmacokinetics (PK) of a heat-stable, inhaled (IH) oxytocin formulation.

methodsThis phase 1, randomized, single-center, single-blind, dose-escalation, fixed-sequence study (NCT02542813) was conducted in healthy, premenopausal, non-pregnant, non-lactating women aged 18-45years. Subjects initially received IM oxytocin 10 international units (IU) on day 1, IH placebo on day 2, and IH oxytocin 50μg on day 3. Subjects were then randomized 4:1 using validated GSK internal software to IH placebo or ascending doses of IH oxytocin (200, 400, 600μg). PK was assessed by comparing systemic exposure (maximum observed plasma concentration, area under the concentration-time curve, and plasma concentrations at 10 and 30min post dose) for IH versus IM oxytocin. Adverse events (AEs), spirometry, laboratory tests, vital signs, electrocardiograms, physical examinations, and cardiac telemetry were assessed.

findingsSubjects were recruited between September 14, 2015 and October 12, 2015. Of the 16 subjects randomized following initial dosing, 15 (IH placebo n=3; IH oxytocin n=12) completed the study. IH (all doses) and IM oxytocin PK profiles were comparable in shape. However, systemic exposure with IH oxytocin 400μg most closely matched IM oxytocin 10IU. Systemic exposure was approximately dose proportional for IH oxytocin. No serious AEs were reported. No clinically significant findings were observed for any safety parameters.

interpretationThese data suggest that similar oxytocin systemic exposure can be achieved with IM and IH administration routes, and no safety concerns were identified with either route. The inhalation route may offer the opportunity to increase access to oxytocin for women giving birth in resource-poor settings.

Indexed as

Administration, InhalationAdultArea Under CurveDrug Administration ScheduleFemaleHealthy VolunteersHumansInjections, IntramuscularOxytocinPremenopauseYoung AdultOxytocinInhaled oxytocinPhase 1PlaceboPostpartum hemorrhage

Identifiers

PMID28781129
PMCPMC5552226
OpenAlexW2738901440

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.