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Nausea

24
Pipeline Programs
12
Companies
12
Clinical Trials
1 recruiting
0
Approved Products

Pipeline by Development Stage

Preclinical
Phase 1
Phase 1/2
Phase 2
Phase 2/3
Phase 3
On Market
0
2
0
7
0
4
11
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Small Molecule
1100%
+ 36 programs with unclassified modality

Competitive Landscape

11 companies ranked by most advanced pipeline stage

MSD
MSDIreland - Ballydine
13 programs
3
1
5
AprepitantPhase 4
AprepitantPhase 4
MK0869, aprepitant / Duration of Treatment: 3 daysPhase 4
MK0869, aprepitant / Duration of Treatment: 3 daysPhase 4
Standard POPhase 4
+8 more programs
Sharp Therapeutics
Sharp TherapeuticsPA - Pittsburgh
13 programs
3
1
5
AprepitantPhase 4
AprepitantPhase 4
MK0869, aprepitant / Duration of Treatment: 3 daysPhase 4
MK0869, aprepitant / Duration of Treatment: 3 daysPhase 4
Standard POPhase 4
+8 more programs
ViiV Healthcare
ViiV HealthcareNC - Durham
1 program
1
OndansetronPhase 41 trial
Active Trials
NCT00429832Completed120Est. Nov 2005
Helsinn
HelsinnIreland - Dublin
1 program
1
Fosaprepitant dimegluminePhase 31 trial
Active Trials
NCT01074697Completed246Est. Apr 2015
AstraZeneca
AstraZenecaCAMBRIDGE, United Kingdom
1 program
1
esomeprazolePhase 3Small Molecule1 trial
Active Trials
NCT00206440Terminated43Est. Feb 2012
Prevail Therapeutics
1 program
1
LY3537021Phase 21 trial
Active Trials
NCT07169851Recruiting204Est. Feb 2027
Sandoz
SandozAustria - Kundl
2 programs
2
Ondansetron HCl 24 mg TabletsPhase 11 trial
Ondansetron HCl 24 mg TabletsPhase 11 trial
Active Trials
NCT00946387Completed26Est. Sep 2004
NCT00947128Completed26Est. Oct 2004
Merck & Co.
Merck & Co.RAHWAY, NJ
2 programs
Development of a Predictive Model for Post-Discharge Nausea and Vomiting (PDNV)N/A1 trial
MK0869, aprepitant / Duration of Treatment: 3 daysPHASE_33 trials
Active Trials
NCT00514878Completed2,000Est. Nov 2008
NCT00090207Completed477Est. Sep 2004
NCT00092196Completed820Est. Dec 2004
+1 more trials
Nielsen BioSciences
Nielsen BioSciencesCA - San Diego
1 program
Sevoflurane-remifentanil anaesthesiaN/A1 trial
Active Trials
NCT00452855Completed160Est. May 2005
Takeda
TakedaTOKYO, Japan
1 program
OndansetronPHASE_21 trial
Active Trials
NCT02006056Completed30Est. Jun 2014
GSK
GSKLONDON, United Kingdom
1 program
OndansetronPHASE_4

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
Merck & Co.MK0869, aprepitant / Duration of Treatment: 3 days
ViiV HealthcareOndansetron
Merck & Co.MK0869, aprepitant / Duration of Treatment: 3 days
HelsinnFosaprepitant dimeglumine
AstraZenecaesomeprazole
Merck & Co.MK0869, aprepitant / Duration of Treatment: 3 days
Prevail TherapeuticsLY3537021
TakedaOndansetron
SandozOndansetron HCl 24 mg Tablets
SandozOndansetron HCl 24 mg Tablets
Merck & Co.Development of a Predictive Model for Post-Discharge Nausea and Vomiting (PDNV)
Nielsen BioSciencesSevoflurane-remifentanil anaesthesia

Clinical Trials (12)

Total enrollment: 5,018 patients across 12 trials

NCT00090207Merck & Co.MK0869, aprepitant / Duration of Treatment: 3 days

Aprepitant for the Prevention of Chemotherapy Induced Nausea and Vomiting (CINV) Associated With Highly Emetogenic Chemotherapy (0869-801)(COMPLETED)

Start: Jan 2004Est. completion: Sep 2004477 patients
Phase 4Completed

A RCT of Ondansetron and Promethazine in the Treatment of Nausea and Vomiting in the Emergency Department

Start: Oct 2003Est. completion: Nov 2005120 patients
Phase 4Completed
NCT00092183Merck & Co.MK0869, aprepitant / Duration of Treatment: 3 days

An Investigational Drug for the Prevention of Chemotherapy-Induced Nausea and Vomiting (MK-0869-071)

Start: Oct 2002Est. completion: Feb 2004866 patients
Phase 4Completed
NCT01074697HelsinnFosaprepitant dimeglumine

Efficacy of Two Antiemetic Regimens in Patients Receiving Radiotherapy and Concomitant Weekly Cisplatin

Start: Apr 2010Est. completion: Apr 2015246 patients
Phase 3Completed

Nexium Study To Suppress Nausea During Chemotherapy

Start: Aug 2005Est. completion: Feb 201243 patients
Phase 3Terminated
NCT00092196Merck & Co.MK0869, aprepitant / Duration of Treatment: 3 days

Study of MK0869 for the Prevention of Chemotherapy-Induced Nausea and Vomiting (0869-071)(COMPLETED)

Start: Dec 2002Est. completion: Dec 2004820 patients
Phase 3Completed

A Study to Evaluate LY3537021 for the Treatment of Nausea and Vomiting Caused by Chemotherapy in Adults With Cancer

Start: Nov 2025Est. completion: Feb 2027204 patients
Phase 2Recruiting

Ondissolve in the Prophylaxis/Rescue of Radiation Induced Nausea and Vomiting

Start: Nov 2013Est. completion: Jun 201430 patients
Phase 2Completed
NCT00947128SandozOndansetron HCl 24 mg Tablets

To Demonstrate the Relative Bioavailability Study of Ondansetron HCl 24 mg Tablets Under Non-Fasting Conditions

Start: Sep 2004Est. completion: Oct 200426 patients
Phase 1Completed
NCT00946387SandozOndansetron HCl 24 mg Tablets

To Demonstrate the Relative Bioavailability Study of Ondansetron HCl 24 mg Tablets Under Fasting Conditions

Start: Sep 2004Est. completion: Sep 200426 patients
Phase 1Completed
NCT00514878Merck & Co.Development of a Predictive Model for Post-Discharge Nausea and Vomiting (PDNV)

Development of a Predictive Model for Post-Discharge Nausea and Vomiting (PDNV)

Start: Aug 2007Est. completion: Nov 20082,000 patients
N/ACompleted
NCT00452855Nielsen BioSciencesSevoflurane-remifentanil anaesthesia

Sevoflurane-Remifentanil Anaesthesia. The Risk of Post Operative Nausea

Start: Jan 2002Est. completion: May 2005160 patients
N/ACompleted

Phase Legend

PreclinicalLab & animal studies
Phase 1Safety & dosing
Phase 2Efficacy testing
Phase 3Large-scale trials
On MarketApproved & available

Key Insights

4 late-stage (Phase 3) programs, potential near-term approvals
1 actively recruiting trials targeting 5,018 patients
12 companies competing in this space

The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.