A Study on 2 Different Combination Tablets of Nirmatrelvir Plus Ritonavir to Compare Them With Marketed Paxlovid in Healthy Participants

NCT ID: NCT06397144

Last Updated: 2025-12-26

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: PHASE1
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-08-15
• Study Completion Date: 2025-12-09

Brief Summary

Medicines that may have different names or be made in different ways but have the same effect on the body are called bioequivalent.

The purpose of this study is to learn about the bioequivalence of nirmatrelvir plus ritonavir after taking 2 different combination tablet forms by mouth. These combination tablets are compared to the tablet formulation that is already in the market. This study will be done under fasted conditions in healthy adult participants.

This study is seeking participants who are:

• Male and non-pregnant female participants aged 18 years and above.
• with a body weight of more than 50 kilograms and Body Mass Index (BMI) between 16 to 32 kilograms per meter squared.
• are healthy as confirmed by medical history, physical examination, laboratory tests.

The study will also look at the safety and tolerability of nirmatrelvir plus ritonavir combination tablet and marketed tablet formulations in healthy adult participants.

The study will consist of 4 treatments:

Treatment A: Single oral dose of nirmatrelvir plus ritonavir 150 (1 × 150)/100 milligrams marketed tablets under fasted conditions (Reference 1) Treatment B (low dose strength): Single oral dose of nirmatrelvir plus ritonavir 150/100 milligrams (2 × [75/50 milligrams]) combination tablets under fasted conditions (Test 1) Treatment C: Single oral dose of nirmatrelvir/ritonavir 300 (2 × 150)/100 milligrams marketed tablets under fasted conditions (Reference 2) Treatment D (high dose strength): Single oral dose of nirmatrelvir/ritonavir 300/100 milligrams (2 × [150/50 milligrams]) combination tablets under fasted conditions (Test 2)

All treatments will be given under fasted conditions. Fasted condition means the participants would not have had anything to eat before taking the medicines.

Around 28 participants will be enrolled in the study. Healthy participants will be tested to see if they can be in the study within 28 days before receiving the study medicine. Selected participants will be admitted to the clinical research unit (CRU) one day before receiving the study medicine and will remain in the CRU until discharge after completing all the treatment periods.

On Day 1 of each period, participants will be given a single dose of study medicine nirmatrelvir/ritonavir 300/100 mg or 150/100 mg by mouth by chance. Study medicine will be given with approximately 240 milliliters of room temperature water under fasted conditions (overnight fast of at least 10 hours and no food until 4 hours after receiving the study medicine). Blood samples will be collected at different times of the day up to 48 hours after taking the study medicine. Participants will be discharged from the CRU on Day 3 of Period 4, after all the study related procedures have been completed.

A follow-up call will be made to participants around 28 to 35 days from receiving the final dose of the study medicine. The study will look at the experiences of participants receiving the study medicine. This will help to understand if the study medicine is safe and effective.

Conditions

Biological Availability; Healthy Participants

Keywords

Coronavirus disease 2019 (COVID-19); Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2); Nirmatrelvir; Paxlovid

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: NONE

Study Groups

Paxlovid commercial tablets A (Low Dose)

Single oral dose of nirmatrelvir/ ritonavir 150 (1 × 150)/100 mg commercial tablets under fasted conditions (Reference 1)

Group Type: ACTIVE_COMPARATOR

Paxlovid

Intervention Type: DRUG

Reference 1

Paxlovid commercial tablets B (High Dose)

Single oral dose of nirmatrelvir/ ritonavir 300 (2 × 150)/100 mg commercial tablets under fasted conditions (Reference 2)

Group Type: ACTIVE_COMPARATOR

Paxlovid

Intervention Type: DRUG

Reference 2

Nirmatrelvir/ritonavir FDC tablets Test formulation 1

Single oral dose of nirmatrelvir /ritonavir 150/100 mg (2 × \[75/50 mg\]) FDC tablets Test formulation 1 (Test 1)

Group Type: EXPERIMENTAL

Nirmatrelvir/ritonavir

Intervention Type: DRUG

Test 1

Nirmatrelvir/ritonavir FDC tablets Test formulation 2

Single oral dose of nirmatrelvir/ ritonavir 300/100 mg (2 × \[150/50 mg\]) FDC tablets Test formulation 2 (Test 2)

Group Type: EXPERIMENTAL

Nirmatrelvir/ritonavir

Intervention Type: DRUG

Test 2

Interventions

Paxlovid

Reference 1

Intervention Type: DRUG

Paxlovid

Reference 2

Intervention Type: DRUG

Nirmatrelvir/ritonavir

Test 1

Intervention Type: DRUG

Nirmatrelvir/ritonavir

Test 2

Intervention Type: DRUG

Other Intervention Names

Nirmatrelvir/ritonavir commercial tablets; Nirmatrelvir/ritonavir commercial tablets; Nirmatrelvir/ritonavir FDC test tablets formulation 1; Nirmatrelvir/ritonavir FDC test tablets formulation 2

Eligibility Criteria

Inclusion Criteria

• Participants who are overtly healthy as determined by medical evaluation including medical history, physical examination, laboratory tests, and standard 12-lead ECG (electrocardiogram).
• Participants who are willing and able to comply with all scheduled visits, treatment plan, laboratory tests, lifestyle considerations, and other study procedures.
• Female participants of childbearing potential must have a negative pregnancy test at screening and on Day -1.
• BMI (Body Mass Index) of 16-32 kg/m2; and a total body weight >50 kg (110 lb).
• Capable of giving signed informed consent, which includes compliance with the requirements and restrictions listed in the ICD (Informed consent Document) and in this protocol.

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).
• Any condition possibly affecting drug absorption (eg, gastrectomy, cholecystectomy).
• History of HIV (Human Immunodeficiency Virus) infection, Hepatitis B, or Hepatitis C; positive testing for HIV, HBsAg (Hepatitis B surface Antigen), HBcAb (Hepatitis B core Antibody) or HCVAb (Hepatitis C Virus Antibody). Hepatitis B vaccination is allowed.
• Any medical or psychiatric condition including recent (within the past year) or active suicidal ideation/behavior or laboratory abnormality or other conditions 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.
• Participants 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.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Pfizer

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Pfizer CT.gov Call Center

Role: STUDY_DIRECTOR

Pfizer

Related Links

https://pmiform.com/clinical-trial-info-request?StudyID=C4671009

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

Other Identifiers

NCT06397144

Identifier Type: REGISTRY

Identifier Source: secondary_id

C4671009

Identifier Type: -

Identifier Source: org_study_id