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Disease

Postoperative Nausea and Vomiting

Late-stage therapeutic developmentEmerging research
1
Publications
23
Clinical trials
2020
Latest publication
Latest activity
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Recent clinical, regulatory, research and industry developments relating to this disease.

What's happening now

An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.

Clinical Milestones11View all 11
+3 more in the activity timeline below
Activity timeline11

Therapeutic landscape

Therapies with a regulatory footing for this condition, alongside the wider set of agents co-studied with it in the literature.

Approved & established therapies
Aprepitantapproved

Approval — Emend 40 mg hard capsules is indicated for the prevention of postoperative nausea and vom… (2003)

Clinical trials

17 sponsors · 6 new · 5 completed in the last 12 months (net +6)

The current development programme across all trial phases.

Clinical programme
23
All trials
6
Active
17
Late-stage
5
Completed
Late-stage studies
Recruiting
Recently completed

Regulatory timeline

Drug regulatory events matched to this condition by indication — EMA.

First approvals
2003emaApprovalAprepitant· Emend 40 mg hard capsules is indicated for the prevention of postoperative nausea and vomiting (PONV) in adults. Emend is also available as 80 mg and 125 mg hard capsules for the prevention of nausea and vomiting associated with highly and moderately emetogenic cancer chemotherapy in adults and adolescents from the age of 12 (see separate Summary of Product Characteristics). Emend is also available as 165 mg hard capsules for the prevention of acute and delayed nausea and vomiting associated with highly emetogenic cisplatin based cancer chemotherapy in adults and the prevention of nausea and vomiting associated with moderately emetogenic cancer chemotherapy in adults. Emend is also available as powder for oral suspension for the prevention of nausea and vomiting associated with highly and moderately emetogenic cancer chemotherapy in children, toddlers and infants from the age of 6 months to less than 12 years. Emend 80 mg, 125 mg, 165 mg hard capsules and Emend powder for oral suspension are given as part of combination therapy. source ↗

European Medicines Agency (CC BY 4.0). Events are matched to this condition by drug indication text — approvals/updates for drugs indicated for it, not disease-specific acts.

Research activity

1 papers

Key research shaping understanding of this disease, combining the latest publications with the most influential evidence.

Major themes1
  • Enhanced Recovery After Surgery1
Leading journals1
  • Acta orthopaedica1
Leading researchers8
  • Gill M1
  • Ljungqvist O1
  • McDonald DA1
  • Middleton RG1
  • Reed M1
  • Sahota O1
  • Wainwright TW1
  • Yates P1
Affiliations (unnormalised)6
  • Glasgow Caledonian University1
  • Golden Jubilee National Hospital1
  • Northumbria Healthcare NHS Foundational Trust1
  • Nottingham University1
  • Nottingham University Hospital1
  • Örebro University1

Reference

Authoritative identity, definition & identifiers.

Defined in MeSH

Emesis and queasiness occurring after anesthesia.

References & data sources
  • Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
  • Clinical trials — ClinicalTrials.gov (U.S. National Library of Medicine)
  • Research activity — Europe PMC (EMBL-EBI) + OpenAlex-derived paper links
  • Related entities are derived from literature co-mention (studied together) — associative, not causal.