Bioequivalence Study for Crizotinib Encapsulated Microsphere Formulation (eMS)

PHASE1CompletedINTERVENTIONAL
Enrollment

25

Participants

Timeline

Start Date

April 16, 2021

Primary Completion Date

December 15, 2021

Study Completion Date

December 15, 2021

Conditions
Healthy Participants
Interventions
DRUG

Crizotinib

A single 250 mg crizotinib dose of the FC formulation

DRUG

Crizotinib

A single 250 mg crizotinib dose of the encapsulated microsphere (eMS) formulation administered by sprinkling the contents into a dry glass vial

DRUG

Crizotinib

A single 250 mg crizotinib dose of the single 250 mg crizotinib dose of the encapsulated microsphere (eMS) formulation (administered as intact capsules) . The intact capsules will be swallowed whole.

Trial Locations (1)

06511

New Haven Clinical Research Unit, New Haven

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY

NCT04856293 - Bioequivalence Study for Crizotinib Encapsulated Microsphere Formulation (eMS) | Biotech Hunter | Biotech Hunter