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Disease

Vomiting

Late-stage therapeutic developmentEmerging research
2
Publications
24
Clinical trials
2018
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 Milestones9View all 9
+1 more in the activity timeline below
Activity timeline9

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
Palonosetronapproved

Approval — Palonosetron Accord is indicated in adults for: the prevention of acute nausea and vomit… (2016)

Granisetronapproved

Approval — Prevention of nausea and vomiting in patients receiving moderately or highly emetogenic c… (2012)

Approval — Prevention of nausea and vomiting associated with highly and moderately emetogenic cancer… (2008)

Aprepitantapproved

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

Clinical trials

18 sponsors · 2 new · 5 completed in the last 12 months (net +2)

The current development programme across all trial phases.

Clinical programme
24
All trials
6
Active
18
Late-stage
6
Completed
Late-stage studies
Recruiting
Recently completed

Regulatory timeline

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

First approvals
2016emaApprovalPalonosetron· Palonosetron Accord is indicated in adults for: the prevention of acute nausea and vomiting associated with highly emetogenic cancer chemotherapy, the prevention of nausea and vomiting associated with moderately emetogenic cancer chemotherapy. Palonosetron Accord is indicated in paediatric patients 1 month of age and older for: The prevention of acute nausea and vomiting associated with highly emetogenic cancer chemotherapy and prevention of nausea and vomiting associated with moderately emetogenic cancer chemotherapy. source ↗
2012emaApprovalGranisetron· Prevention of nausea and vomiting in patients receiving moderately or highly emetogenic chemotherapy, with or without cisplatin, for up to five consecutive days. Sancuso may be used in patients receiving their first chemotherapy regimen or in patients who have previously received chemotherapy. source ↗
2008emaApprovalFosaprepitant· Prevention of nausea and vomiting associated with highly and moderately emetogenic cancer chemotherapy in adults and paediatric patients aged 6 months and older. Ivemend 150 mg is given as part of a combination therapy. source ↗
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

2 papers

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

Publications over time
20142018
Major themes1
  • Glucagon-Like Peptide-1 Receptor Agonists1
Leading journals2
  • Blood1
  • Molecular metabolism1
Leading researchers8
  • Alsina-Fernandez J1
  • Benson CT1
  • Bokvist KB1
  • Briere DA1
  • Burke JM1
  • Cabrera O1
  • Chen L1
  • Clementi R1
Affiliations (unnormalised)3
  • Duke University Medical Center1
  • Lilly Corporate Center1
  • Sarah Cannon Research Institute/Tennessee Oncology1

Reference

Authoritative identity, definition & identifiers.

Defined in MeSH

The forcible expulsion of the contents of the STOMACH through the MOUTH.

Identifiers
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.