MedPath

Ondansetron

Generic Name
Ondansetron
Brand Names
Zofran, Zuplenz
Drug Type
Small Molecule
Chemical Formula
C18H19N3O
CAS Number
99614-02-5
Unique Ingredient Identifier
4AF302ESOS
Background

A competitive serotonin type 3 receptor antagonist. It is effective in the treatment of nausea and vomiting caused by cytotoxic chemotherapy drugs, including cisplatin, and has reported anxiolytic and neuroleptic properties.

Having been developed in the 1980s by GlaxoSmithKline and approved by the US FDA since January 1991, ondansetron has demonstrated a long history of use and efficacy. Commonly formulated as oral tablets, orally disintegrating tablets (ODT), and injections, and available as generic products as well, ondansetron continues to see contemporary innovations in its formulation and use, including the development of orally soluble films that are both discreet in administration and less of a burden in comparison to having patients attempt to swallow pills during emesis.

The FDA withdrew its approval for the use of all intravenous drug products containing more than 16 mg of ondansetron hydrochloride in a single dose, due to a high risk of QT prolongation.

Indication

In the adult patient population:

i) orally administered ondansetron tablets and orally disintegrating tablets (ODT) are indicated for:

- the prevention of nausea and vomiting associated with emetogenic cancer chemotherapy, including high dose (ie. greater than or equal to 50 mg/m2) cisplatin therapy, and radiotherapy, and

- the prevention and treatment of postoperative nausea and vomiting

ii) intravenously administered ondansetron injection formulations are indicated for:

- the prevention of nausea and vomiting associated with emetogenic cancer chemotherapy, including high dose (ie. greater than or equal to 50 mg/m2) cisplatin therapy, and

- the prevention and treatment of postoperative nausea and vomiting

In the pediatric (4-18 years of age) patient population:

i) ondansetron was effective and well tolerated when given to children 4-12 years of age for the treatment of post-chemotherapy induced nausea and vomiting,

ii) ondansetron tablets, ondansetron ODT, ondansetron injection are not indicated for the treatment of children 3 years of age or younger,

iii) ondansetron tablets, ondansetron ODT, ondansetron injection are not indicated for use in any age group of the pediatric population for the treatment of post-radiotherapy induced nausea and vomiting, and

iV) ondansetron tablets, ondansetron ODT, ondansetron injection are not indicated for use in any age group of the pediatric population for the treatment of postoperative nausea and vomiting

In the geriatric (>65 years of age) patient population:

i) efficacy and tolerance of ondansetron were similar to that observed in younger adults for the treatment of post-chemotherapy and radiotherapy-induced nausea and vomiting, and

ii) clinical experience in the use of ondansetron in the prevention and treatment of postoperative nausea and vomiting is limited and is not indicated for use in the geriatric patient population

Associated Conditions
Chemotherapy-Induced Nausea and Vomiting, Cholestatic pruritus, Post Operative Nausea and Vomiting (PONV), Radiation-Induced Nausea and Vomiting, Uremic Pruritus, Severe Hyperemesis gravidarum
Associated Therapies
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Phase 3
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Conditions
Postoperative Nausea and Vomiting
Interventions
First Posted Date
2016-07-13
Last Posted Date
2016-07-13
Lead Sponsor
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Target Recruit Count
99
Registration Number
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Phase 2
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Conditions
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Interventions
First Posted Date
2016-04-08
Last Posted Date
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Lead Sponsor
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Target Recruit Count
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Registration Number
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Locations
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First Posted Date
2016-01-20
Last Posted Date
2016-01-20
Lead Sponsor
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Registration Number
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Phase 4
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Conditions
Headache
Interventions
First Posted Date
2016-01-15
Last Posted Date
2017-12-11
Lead Sponsor
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Target Recruit Count
54
Registration Number
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Locations
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University Medical Center of Southern Nevada, Las Vegas, Nevada, United States

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Not Applicable
Completed
Conditions
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Interventions
First Posted Date
2015-12-09
Last Posted Date
2019-03-07
Lead Sponsor
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Target Recruit Count
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Registration Number
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Locations
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Phase 3
Conditions
Acute Gastroenteritis
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Interventions
First Posted Date
2015-12-02
Last Posted Date
2015-12-02
Lead Sponsor
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Target Recruit Count
250
Registration Number
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Not Applicable
Completed
Conditions
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Interventions
First Posted Date
2015-12-01
Last Posted Date
2021-03-24
Lead Sponsor
The University of Texas Health Science Center at San Antonio
Target Recruit Count
51
Registration Number
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Phase 1
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Conditions
Schizophrenia
Interventions
Drug: TAK-058
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Drug: TAK-058 Placebo
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First Posted Date
2015-11-25
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Registration Number
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Phase 3
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Conditions
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Interventions
Procedure: Transversus Abdominis Plane (TAP) block
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Drug: Acetominophen
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First Posted Date
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Lead Sponsor
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Target Recruit Count
120
Registration Number
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Locations
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Phase 4
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Conditions
Postoperative Nausea and Vomiting
Interventions
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Last Posted Date
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Lead Sponsor
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Target Recruit Count
80
Registration Number
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Locations
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