A Study to Learn How Different Amounts of the Study Medicine Called PF-07328948 Are Tolerated and Act in the Body in Healthy Adults

Healthy Clinical Trial

Official title:

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

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05807490
• Other study ID #: C4921002
• Secondary ID: 2023-509054-54-0
• Status: Recruiting
• Phase: Phase 1
• Start date: April 5, 2023
• Est. completion date: July 10, 2024

Study information

• Verified date: April 2024
• Source: Pfizer
• Contact: Pfizer CT.gov Call Center
• Phone: 1-800-718-1021
• Email: ClinicalTrials.gov_Inquiries[@]pfizer.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 132
• Est. completion date: July 10, 2024
• Est. primary completion date: July 10, 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

1. 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.

2. 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.

3. Participants who are willing and able to comply with all scheduled visits, treatment plan, laboratory tests, lifestyle considerations, and other study procedures.

4. Capable of giving signed informed consent, which includes compliance with the requirements and restrictions listed in the ICD and in this protocol.

Exclusion Criteria:

1. 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.

2. 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.

3. 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.

4. 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.

5. 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.

6. 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).

7. Evidence of a prothrombotic state as evidenced by any of the following:

• History of DVT, pulmonary embolism or arterial thrombosis.

• Known genetic predisposition (Factor V Leiden, prothrombin G20210A, Protein C/S deficiency, antithrombin deficiency) based on medical history. Genetic testing at screening is not required.

• ANY of the following abnormalities in clinical laboratory tests at screening, as assessed by the study specific laboratory and confirmed by a single repeat test if deemed necessary:

• presence of anti-phospholipid antibodies ("Positive" lab result for anticardiolipin, IgA, IgG or IgM)

• Protein C activity < LLN of laboratory reference range

• Protein S activity < LLN of laboratory reference range

• Free Protein S antigen < LLN of laboratory reference range

• Antithrombin activity < LLN of laboratory reference range

• Positive test for APC resistance (Resistance Ratio < LLN of laboratory reference range)

• Plasma fibrinogen > ULN of laboratory reference range

• D-dimer = 500 ng/ml (= 0.50 ug/ml)

8. A positive urine drug test.

9. Screening supine BP =140 mm Hg (systolic) or =90 mm Hg (diastolic), following at least 5 minutes of supine rest.

10. Renal impairment as defined by an eGFR <75 mL/min/1.73m2 calculated using CKD EPI SCr formulas.

11. Standard 12-lead ECG that demonstrates clinically relevant abnormalities that may affect participant safety or interpretation of study results (eg, QTcF >450 ms, complete LBBB, signs of an acute or indeterminate age myocardial infarction, STT interval changes suggestive of myocardial ischemia, second- or third-degree AV block, or serious bradyarrhythmias or tachyarrhythmias). If the uncorrected QT interval is >450 ms, this interval should be rate corrected using the Fridericia method only and the resulting QTcF should be used for decision-making and reporting.

12. Participants with ANY of the following abnormalities in clinical laboratory tests at screening, as assessed by the study specific laboratory and confirmed by a single repeat test, if deemed necessary:

• AST or ALT level =1.5× ULN;

• Total bilirubin level =1.5 × ULN; participants with a history of Gilbert's syndrome may have direct bilirubin measured and would be eligible for this study provided the direct bilirubin level is =ULN.

13. Prior exposure to PF-07328948.

14. History of alcohol abuse or binge drinking and/or any other illicit drug use or dependence within 6 months of Screening. Binge drinking is defined as a pattern of 5 (male) and 4 (female) or more alcoholic drinks in about 2 hours. As a general rule, alcohol intake should not exceed 14 units per week (1 unit = 8 ounces (240 mL) beer, 1 ounce (30 mL) of 40% spirit, or 3 ounces (90 mL) of wine).

15. Investigator site staff directly involved in the conduct of the study and their family members, site staff otherwise supervised by the investigator, and sponsor and sponsor delegate employees directly involved in the conduct of the study and their family members.

16. Use of tobacco or nicotine-containing products in excess of the equivalent of 5 cigarettes/day or 2 chews of tobacco/day.

Related Conditions & MeSH terms

• Healthy

Intervention

Drug:
• PF-07328948
PF-07328948 will be administered as oral suspensions every 12 hour (BID) over 14 days
• Placebo
Placebo will be administered as oral suspensions BID over 14 days
• PF-07328948
PF-07328948 will be administered as oral suspensions daily (QD) over 14 days
• Placebo
Placebo will be administered as oral suspensions QD over 14 days
• PF-07328948
PF-07328948 will be administered as oral suspensions every QD over 14 days
• Placebo
Placebo will be administered as oral suspensions QD over 14 days
• PF-07328948
PF-07328948 will be administered as oral suspensions QD over 14 days
• Placebo
Placebo will be administered as oral suspensions QD over 14 days
• PF-07328948
PF-07328948 will be administered as oral suspensions QD over 14 days
• Placebo
Placebo will be administered as oral suspensions QD over 14 days
• PF-07328948
PF-07328948 will be administered as oral suspensions every 12 hour (BID) or everyday (QD) over 14 days
• Placebo
Placebo will be administered as oral suspensions every 12 hour (BID) or everyday (QD) over 14 days
• PF-07328948
PF-07328948 will be administered as oral suspensions QD over 14 days
• Placebo
Placebo will be administered as oral suspensions QD over 14 days
• PF-07328948
PF-07328948 will be administered as oral suspensions every 12 hour (BID) or daily (QD) over 14 days
• Placebo
Placebo will be administered as oral suspensions every 12 hour (BID) or daily (QD) over 14 days
• PF-07328948
Single doses of PF-07328948 will be administered as oral suspension (single dose) and oral tablet (single dose) under fed and fasted condition
• PF-07328948
PF-07328948 will be administered as oral suspensions QD over 14 days
• Placebo
Placebo will be administered as oral suspensions QD over 14 days
• PF-07328948
PF-07328948 will be administered as oral suspensions every 12 hour (BID) or daily (QD) over 14 days
• Placebo
Placebo will be administered as oral suspensions every 12 hour (BID) or daily (QD) over 14 days
• PF-07328948
PF-07328948 will be administered as oral suspensions every 12 hour (BID) or daily (QD) over 14 days

Locations

Country	Name	City	State
Belgium	Pfizer Clinical Research Unit - Brussels	Brussels	Bruxelles-capitale, Région DE
United States	New Haven Clinical Research Unit	New Haven	Connecticut

Sponsors (1)

Lead Sponsor	Collaborator
Pfizer

Countries where clinical trial is conducted

United States,  Belgium, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Part A: Number of Participants With Treatment Emergent Treatment-Related Adverse Events (AEs)		Baseline up to 35 days after last dose of study intervention (approximately 11 weeks)
Primary	Part A: Number of Participants With Clinical Laboratory Abnormalities		Baseline up to 10 days after last dose of study intervention (approximately 7 weeks).
Primary	Part A: Number of Participants With Clinically Significant Change From Baseline in Vital Signs		Baseline up to 10 days after last dose of study intervention (approximately 7 weeks)
Primary	Part A: Number of Participants With Change From Baseline in Electrocardiogram (ECG) Findings		Baseline up to 10 days after last dose of study intervention (approximately 7 weeks)
Primary	Part A: Number of Participants With Change From Baseline in Physical Examination Findings		Baseline up to 10 days after last dose of study intervention (approximately 7 weeks)
Primary	Part A: Number of Participants With Cardiac Rhythms of Potential Clinical Concern Assessed By Telemetry		0 to 8 hours post-dose on Day 1
Primary	Part A: Number of Participants With Cardiac Rhythms of Potential Clinical Concern Assessed By Telemetry		0 to 8 hours post-dose on Day 14
Primary	Part B: Maximum Observed Plasma Concentration (Cmax) of PF-07328948 Tablet Formation and Oral Suspension		Predose, 0.5, 1, 1.5, 2, 4, 6, 8, 12, 16, 24, 36, 48, and 72 hours post dose on Day 1
Primary	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		Predose, 0.5, 1, 1.5, 2, 4, 6, 8, 12, 16, 24, 36, 48, and 72 hours post dose on Day 1
Primary	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		Predose, 0.5, 1, 1.5, 2, 4, 6, 8, 12, 16, 24, 36, 48, and 72 hours post dose on Day 1
Secondary	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 1
Secondary	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
Secondary	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 1
Secondary	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
Secondary	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 1
Secondary	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
Secondary	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)
Secondary	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)
Secondary	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)
Secondary	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
Secondary	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
Secondary	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
Secondary	Part B: Number of Participants With Treatment Emergent Treatment-Related Adverse Events (AEs)		Baseline up to 35 days post dose of study intervention
Secondary	Part B: Number of Participants With Clinical Laboratory Abnormalities		Baseline up to 4 days post dose of study intervention
Secondary	Part B: Number of Participants With Clinically Significant Change From Baseline in Vital Signs		Baseline up to 4 days post dose of study intervention
Secondary	Part B: Number of Participants With Change From Baseline in Electrocardiogram (ECG) Findings		Baseline up to 4 days post dose of study intervention
Secondary	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
Secondary	Part B: % of administered dose excreted in urine at each specified time interval		Days 1 to 11 at 24-hour intervals post-dose
Secondary	Part B: Total % of PF-07328948 dose recovered in urine		Days 1 to 11 at 24-hour intervals post-dose
Secondary	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
Secondary	Part B: Total % of PF-07328948 dose recovered in feces		Days 1 to 11 at 24-hour intervals post-dose

External Links

•   To obtain contact information for a study center near you, click here.