Relative Bioavailability Study of PF-07321332/Ritonavir Oral Powder Relative to the Commercial Tablets in Healthy Participants

Pfizer

Status and phase: Completed; Phase 1

Conditions: Bioavailability

Treatments: Drug: PF-07321332/ritonavir

Study type: Interventional

Funder types: Industry

Identifiers

NCT05263921

C4671024

Details and patient eligibility

About

The purpose of this study is to estimate the relative bioavailability of PF-07321332/ritonavir oral powder relative to the commercial tablet formulation under fasted condition in healthy adult participants. The study will also assess the effect of 3 different food vehicles on the relative bioavailability of the PF-07321332/ritonavir oral powder formulation as well as the safety, tolerability, and palatability of PF-07321332/ritonavir oral powder in healthy adult participants.

Enrollment: 12 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Participants who are overtly healthy as determined by medical evaluation including medical history, physical examination (PE), laboratory tests, vital signs and standard 12 lead ECGs.
• Body mass index (BMI) of 17.5 to 30.5 kg/m2; and a total body weight >50 kg (110 lb).
• Participants who are willing and able to comply with all scheduled visits, treatment plan, laboratory tests, lifestyle considerations, and other study procedures

Exclusion criteria

• Positive test result for SARS-CoV-2 infection at the time of Screening or Day -1.
• Evidence or history of clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurological, or allergic disease (including drug allergies, but excluding untreated, asymptomatic, seasonal allergies at the time of dosing).
• Clinically relevant abnormalities requiring treatment (eg, acute myocardial infarction, unstable ischemic conditions, evidence of ventricular dysfunction, serious tachy or brady arrhythmias) or indicating serious underlying heart disease (eg, prolonged PR interval, cardiomyopathy, heart failure greater than New York Heart Association (NYHA) 1, underlying structural heart disease, Wolff Parkinson-White syndrome).
• Any condition possibly affecting drug absorption (eg, gastrectomy, cholecystectomy).
• History of human immunodeficiency virus (HIV) infection, hepatitis B, or hepatitis C; positive testing for HIV, hepatitis B surface antigen (HBsAg), or hepatitis B surface antibody (HCVAb). Hepatitis B vaccination is allowed.
• Use of prescription or nonprescription drugs and dietary and herbal supplements within 7 days or 5 half lives (whichever is longer) prior to the first dose of study intervention.
• Participant who have received a COVID-19 vaccine within 7 days before screening or admission, or who are to be vaccinated with a COVID-19 vaccine at any time during the study confinement period.
• A positive urine drug test.

Trial design

Primary purpose: Basic Science

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: None (Open label)

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12 participants in 4 patient groups

Treatment A: PF-07321332/ritonavir

Active Comparator group

Description:

PF-07321332 ritonavir

Treatment:

Drug: PF-07321332/ritonavir

Drug: PF-07321332/ritonavir

Drug: PF-07321332/ritonavir

Drug: PF-07321332/ritonavir

Treatment B: PF-07321332/ritonavir

Experimental group

Description:

PF-07321332/ritonavir mixed with water

Treatment:

Drug: PF-07321332/ritonavir

Drug: PF-07321332/ritonavir

Drug: PF-07321332/ritonavir

Drug: PF-07321332/ritonavir

Treatment C: PF-07321332/ritonavir

Experimental group

Description:

PF-07321332/ritonavir mixed with applesauce

Treatment:

Drug: PF-07321332/ritonavir

Drug: PF-07321332/ritonavir

Drug: PF-07321332/ritonavir

Drug: PF-07321332/ritonavir

Treatment D: PF-07321332/ritonavir

Experimental group

Description:

PF-07321332/ritonavir mixed with vanilla pudding

Treatment:

Drug: PF-07321332/ritonavir

Drug: PF-07321332/ritonavir

Drug: PF-07321332/ritonavir

Drug: PF-07321332/ritonavir