A PHASE 1, RANDOMIZED, DOUBLE-BLIND, SPONSOR-OPEN, PLACEBO-CONTROLLED, PARALLEL STUDY TO EVALUATE THE SAFETY, TOLERABILITY, PHARMACOKINETICS, AND PHARMACODYNAMICS OF MULTIPLE ASCENDING ORAL DOSES OF PF-07328948 IN HEALTHY ADULT PARTICIPANTS
Overview
- Phase
- Phase 1
- Intervention
- PF-07328948
- Conditions
- Healthy
- Sponsor
- Pfizer
- Enrollment
- 86
- Locations
- 2
- Primary Endpoint
- Part A: Number of Participants With Treatment Emergent Treatment-Related Adverse Events (AEs)
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
This study has two parts: Part A and Part B.
The purpose of Part A of this study is to learn about the safety, tolerability, and how PF-07328948 is processed by the body when multiple doses of PF-07328948 are given to healthy participants.
The purpose of Part B of this study is to understand the amount of PF-07328948 that would be available in the body after taking a single pill. The amount will be compared to the amount of PF-07328948 in a suspension in healthy adults.
Part B will be conducted if the results of Part A support further study of PF-07328948.
The study is seeking participants who:
- are females who are not able to give birth to a child of 18 years of age or older.
- are males of 18 years of age or older.
- have a BMI of 20.0 to 35.0 kg/m2.
- have total body weight of more than 50 kg (110 lbs).
Participants in Part A will be randomly selected to receive either PF-07328948 or placebo (a pill that has no medicine in it).
Participants in Part B will receive PF-07328948 as suspension and tablet form, both taken by mouth after food or during fasting.
For a given participant in Part A, the total study is going to last up to about 12 weeks. This includes from the time of selection till the last follow-up phone call. The participants will be selected if they are fit for the study 28 days before the first dose of the study medicines. Participants who are selected will be admitted to the study site on Day -2 for around 19 days. Following discharge, participants will return for an on-site follow-up visit 7 to 10 days after receiving the final dose of the study medicine. The follow-up contact may be via a telephone call and will happen 28 to 35 days after the final dose of study medicine is given.
For a given participant in Part B, the total study is going to last up to about 10-12 weeks. Participants will stay overnight at the CRU for 23 days (Sequence 1) or 18 days (Sequence 2), starting with check-in. In Sequence 1, there will be a minimum of 10 days between doses in Period 1 and 2, and at least 7 days between doses in Period 2 and Period 3. In Sequence 2, there will be a minimum of 7 days between each dose.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Female participants of non-childbearing potential and males must be 18 to 60 years of age for Part A and 18 to 65 years of age for Parts B at the time of signing the ICD, overtly healthy as determined by medical evaluation including medical history, physical exam, laboratory tests, and cardiac monitoring.
- •BMI of 20.0 to 35.0 kg/m2 and a total body weight \>50 kg (110 lbs) for Part A. BMI of 17.5 to 35.0 kg/m2 and a total body weight \>50 kg (110 lbs) for Part B.
- •Participants who are willing and able to comply with all scheduled visits, treatment plan, laboratory tests, lifestyle considerations, and other study procedures.
- •Capable of giving signed informed consent, which includes compliance with the requirements and restrictions listed in the ICD and in this protocol.
Exclusion Criteria
- •Evidence or history of clinically significant hematological (including prothrombic/coagulopathic states), 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).
- •Any condition possibly affecting drug absorption (eg, gastrectomy, cholecystectomy).
- •History of HIV infection, hepatitis B, or hepatitis C; positive testing for HIV, HBsAg, HBcAb, or HCVAb. Hepatitis B vaccination is allowed.
- •Part B only: History of irregular bowel movements including irritable bowel syndrome or frequent episodes of diarrhea or constipation (defined as less than 1 bowel movement on average every 2 days) or lactose intolerance.
- •Other medical or psychiatric condition including recent (within the past year) or active suicidal ideation/behavior or laboratory abnormality or other conditions or situations related to COVID-19 pandemic that may increase the risk of study participation or, in the investigator's judgment, make the participant inappropriate for the study.
- •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.
- •Receipt of a COVID-19 vaccine within 7 days before screening or within 7 days before any visit in which a safety lab is planned. Vaccination with a COVID 19 vaccine that occurs greater than 7 days from either screening or any visit in which a safety lab is planned is permitted.
- •Previous administration with an investigational product (drug or vaccine) within 30 days (or as determined by the local requirement) or 5 half-lives preceding the first dose of study intervention used in this study (whichever is longer).
- •Evidence of a prothrombotic state as evidenced by any of the following:
- •History of DVT, pulmonary embolism or arterial thrombosis.
Arms & Interventions
PF-07328948 and Placebo (Cohort 1)
Dose level 1: Multiple dose administration of PF-07328948 and placebo over 14 days in healthy participants; 8 participants will receive PF-07328948 and 2 will receive placebo
Intervention: PF-07328948
PF-07328948 and Placebo (Cohort 1)
Dose level 1: Multiple dose administration of PF-07328948 and placebo over 14 days in healthy participants; 8 participants will receive PF-07328948 and 2 will receive placebo
Intervention: Placebo
PF-07328948 and Placebo (Cohort 2)
Dose level 2: Multiple dose administration of PF-07328948 and placebo over 14 days in healthy participants; 8 participants will receive PF-07328948 and 2 will receive placebo
Intervention: PF-07328948
PF-07328948 and Placebo (Cohort 2)
Dose level 2: Multiple dose administration of PF-07328948 and placebo over 14 days in healthy participants; 8 participants will receive PF-07328948 and 2 will receive placebo
Intervention: Placebo
PF-07328948 and Placebo (Cohort 3)
Dose level 3: Multiple dose administration of PF-07328948 and placebo over 14 days in healthy participants; 8 participants will receive PF-07328948 and 2 will receive placebo
Intervention: PF-07328948
PF-07328948 and Placebo (Cohort 3)
Dose level 3: Multiple dose administration of PF-07328948 and placebo over 14 days in healthy participants; 8 participants will receive PF-07328948 and 2 will receive placebo
Intervention: Placebo
PF-07328948 and Placebo (Cohort 4)
Dose level 4: Multiple dose administration of PF-07328948 and placebo over 14 days in healthy participants; 8 participants will receive PF-07328948 and 2 will receive placebo
Intervention: PF-07328948
PF-07328948 and Placebo (Cohort 4)
Dose level 4: Multiple dose administration of PF-07328948 and placebo over 14 days in healthy participants; 8 participants will receive PF-07328948 and 2 will receive placebo
Intervention: Placebo
PF-07328948 and Placebo (Cohort 5)
Dose level 5: Multiple dose administration of PF-07328948 and placebo over 14 days in healthy participants; 8 participants will receive PF-07328948 and 2 will receive placebo
Intervention: PF-07328948
PF-07328948 and Placebo (Cohort 5)
Dose level 5: Multiple dose administration of PF-07328948 and placebo over 14 days in healthy participants; 8 participants will receive PF-07328948 and 2 will receive placebo
Intervention: Placebo
PF-07328948 and Placebo (Cohort 10)
Optional cohort - Multiple dose administration of PF-07328948 and placebo over 14 days in healthy Japanese participants; 5 participants will receive PF-07328948 and 1 will receive placebo
Intervention: PF-07328948
PF-07328948 and Placebo (Cohort 10)
Optional cohort - Multiple dose administration of PF-07328948 and placebo over 14 days in healthy Japanese participants; 5 participants will receive PF-07328948 and 1 will receive placebo
Intervention: Placebo
PF-07328948 and Placebo (Cohort 7)
Dose level 7: Multiple dose administration of PF-07328948 and placebo over 14 days in healthy participants; 8 participants will receive PF-07328948 and 2 will receive placebo
Intervention: PF-07328948
PF-07328948 and Placebo (Cohort 7)
Dose level 7: Multiple dose administration of PF-07328948 and placebo over 14 days in healthy participants; 8 participants will receive PF-07328948 and 2 will receive placebo
Intervention: Placebo
PF-07328948 and Placebo (Cohort 8)
Optional cohort - Dose level TBD. Multiple dose administration of PF-07328948 and placebo over 14 days in healthy participants; 8 participants will receive PF-07328948 and 2 will receive placebo
Intervention: PF-07328948
PF-07328948 and Placebo (Cohort 8)
Optional cohort - Dose level TBD. Multiple dose administration of PF-07328948 and placebo over 14 days in healthy participants; 8 participants will receive PF-07328948 and 2 will receive placebo
Intervention: Placebo
PF-07328948 oral tablet and oral suspension (Cohort 11)
Assessment of relative bioavailability PF-07328948 oral tablet compared to PF-07328948 oral suspension under fed and fasted condition; 12 participants will be enrolled, and 6 participants randomized to 1 of 2 sequences
Intervention: PF-07328948
PF-07328948 and Placebo (Cohort 6)
Dose level 6: Multiple dose administration of PF-07328948 and placebo over 14 days in healthy participants; 8 participants will receive PF-07328948 and 2 will receive placebo
Intervention: PF-07328948
PF-07328948 and Placebo (Cohort 6)
Dose level 6: Multiple dose administration of PF-07328948 and placebo over 14 days in healthy participants; 8 participants will receive PF-07328948 and 2 will receive placebo
Intervention: Placebo
PF-07328948 and Placebo (Cohort 9)
Optional cohort - Dose level TBD. Multiple dose administration of PF-07328948 and placebo over 14 days in healthy participants; 8 participants will receive PF-07328948 and 2 will receive placebo
Intervention: PF-07328948
PF-07328948 and Placebo (Cohort 9)
Optional cohort - Dose level TBD. Multiple dose administration of PF-07328948 and placebo over 14 days in healthy participants; 8 participants will receive PF-07328948 and 2 will receive placebo
Intervention: Placebo
Outcomes
Primary Outcomes
Part A: Number of Participants With Treatment Emergent Treatment-Related Adverse Events (AEs)
Time Frame: Baseline up to 35 days after last dose of study intervention (approximately 11 weeks)
Part A: Number of Participants With Change From Baseline in Electrocardiogram (ECG) Findings
Time Frame: Baseline up to 10 days after last dose of study intervention (approximately 7 weeks)
Part A: Number of Participants With Clinical Laboratory Abnormalities
Time Frame: Baseline up to 10 days after last dose of study intervention (approximately 7 weeks).
Part B: Area Under the Plasma Concentration-time Curve from Time 0 to Extrapolated Infinite Time (AUCinf) of PF-07328948 Tablet Formation and Oral Suspension
Time Frame: Predose, 0.5, 1, 1.5, 2, 4, 6, 8, 12, 16, 24, 36, 48, and 72 hours post dose on Day 1
Part A: Number of Participants With Clinically Significant Change From Baseline in Vital Signs
Time Frame: Baseline up to 10 days after last dose of study intervention (approximately 7 weeks)
Part A: Number of Participants With Cardiac Rhythms of Potential Clinical Concern Assessed By Telemetry
Time Frame: 0 to 8 hours post-dose on Day 14
Part B: Maximum Observed Plasma Concentration (Cmax) of PF-07328948 Tablet Formation and Oral Suspension
Time Frame: Predose, 0.5, 1, 1.5, 2, 4, 6, 8, 12, 16, 24, 36, 48, and 72 hours post dose on Day 1
Part B: Area Under the Plasma Concentration-time Curve from Time 0 to the Time of the Last Quantifiable Concentration (AUClast) of PF-07328948 Tablet Formation and Oral Suspension
Time Frame: Predose, 0.5, 1, 1.5, 2, 4, 6, 8, 12, 16, 24, 36, 48, and 72 hours post dose on Day 1
Part A: Number of Participants With Change From Baseline in Physical Examination Findings
Time Frame: Baseline up to 10 days after last dose of study intervention (approximately 7 weeks)
Secondary Outcomes
- Part A: Renal Clearance of PF-07328948(On Day 14, urine collection for PK to occur over 0-tau, according to dosing frequency (ie, 0-12 hours for 12 hour dosing interval; 0-24 hours for QD dosing interval))
- Part B: Area Under the Plasma Concentration-time Curve from Time 0 to the Time of the Last Quantifiable Concentration (AUClast) of PF-07328948 Tablet Formation Under Fasted and Fed Condition(predose, 0.5, 1, 1.5, 2, 4, 6, 8, 12, 16, 24, 36, 48, and 72 hours post dose on Day 1)
- Part B: Number of Participants With Treatment Emergent Treatment-Related Adverse Events (AEs)(Baseline up to 35 days post dose of study intervention)
- Part B: Maximum Observed Plasma Concentration (Cmax) of PF-07328948 Tablet Formation Under Fasted and Fed Condition(predose, 0.5, 1, 1.5, 2, 4, 6, 8, 12, 16, 24, 36, 48, and 72 hours post dose on Day 1)
- Part A: Time to Reach Maximum Observed Plasma Concentration (Tmax) of PF-07328948(predose, 0.25, 0.5, 1, 1.5, 2, 4, 8, 12, 24, 36, 38, and 72 hours post dose on Day 14)
- Part A: Amount of PF-07328948 Excreted Unchanged in Urine Over the Dosing Interval Tau (Aetau)(On Day 14, urine collection for PK to occur over 0-tau, according to dosing frequency (ie, 0-12 hours for 12 hour dosing interval; 0-24 hours for 24 hour dosing interval))
- Part B: Area Under the Plasma Concentration-time Curve from Time 0 to Extrapolated Infinite Time (AUCinf) of PF-07328948 Tablet Formation Under Fasted and Fed Condition(predose, 0.5, 1, 1.5, 2, 4, 6, 8, 12, 16, 24, 36, 48, and 72 hours post dose on Day 1)
- Part B: Number of Participants With Clinical Laboratory Abnormalities(Baseline up to 4 days post dose of study intervention)
- Part B: Number of Participants With Clinically Significant Change From Baseline in Vital Signs(Baseline up to 4 days post dose of study intervention)
- Part B: Number of Participants With Change From Baseline in Electrocardiogram (ECG) Findings(Baseline up to 4 days post dose of study intervention)
- Part B: % of administered dose excreted in urine at each specified time interval(Days 1 to 11 at 24-hour intervals post-dose)
- Part B: Total % of PF-07328948 dose recovered in urine(Days 1 to 11 at 24-hour intervals post-dose)
- Part B: % of administered PF-07328948 dose excreted in feces at each specified time interval(Days 1 to 11 at 24-hour intervals post-dose)
- Part A: Maximum Observed Plasma Concentration (Cmax) of PF-07328948(predose, 0.25, 0.5, 1, 1.5, 2, 4, 8, 12, 24, 36, 38, and 72 hours post dose on Day 14)
- Part A: Area Under the Plasma Concentration-Time Curve From Time 0 to Dosing Interval (tau) (AUCtau) of PF-07328948(predose, 0.25, 0.5, 1, 1.5, 2, 4, 8, 12, 24, 36, 38, and 72 hours post dose on Day 14)
- Part A: Percentage of Dose of PF-07328948 Excreted Unchanged in the Urine Over the Dosing Interval Tau (Aetau%)(On Day 14, urine collection for PK to occur over 0-tau, according to dosing frequency (ie, 0-12 hours for 12 hour dosing interval; 0-24 hours for 24 hour dosing interval))
- Part B: Number of Participants With Clinically-Significant Change From Baseline in Physical Examination Findings(Baseline up to 35 days post dose of study intervention)
- Part B: Total % of PF-07328948 dose recovered in feces(Days 1 to 11 at 24-hour intervals post-dose)