Expired Study
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Woburn, Massachusetts 01801


An oral-liquid, pediatric form of crizotinib designed for use by pediatric patients is being tested for its' palatability in adults.

Study summary:

Taste assessment of new formulation. Subjects will not ingest the drug.


Inclusion Criteria: - Healthy male and/or female of non childbearing potential subjects between the ages of 18 and 75 years, inclusive. - Subjects must be trained sensory panelists. - An informed consent document signed and dated by the subject or a legally acceptable representative. - Subjects who are willing and able to comply with scheduled visits, product evaluations, laboratory tests, and other study procedures. Exclusion Criteria: - A history of clinically significant hematological, renal, endocrine, pulmonary , glaucoma, gastrointestinal, cardiovascular, hepatic, psychiatric, neurologic, allergic disease (excluding untreated, asymptomatic seasonal allergies at the time of product evaluation) as evaluated through a medical history. - A history of hypersensitivity to any inactive ingredients employed in the formulation(s). - Receiving treatment with an investigational drug within 28 days preceding any of the product evaluations for this study. - Participation in a product taste evaluation (ie, 'sip and spit' type taste evaluation) involving an active pharmaceutical ingredient (API) within 5 half lives of that API. - Unwilling or unable to comply with the Lifestyle guidelines described in this protocol.



Primary Contact:

Study Director
Pfizer CT.gov Call Center

Backup Contact:


Location Contact:

Woburn, Massachusetts 01801
United States

There is no listed contact information for this specific location.

Site Status: N/A

Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

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