A Study Evaluating Drug Drug Interaction Between Milvexian and Atorvastatin in Healthy Participants

NCT ID: NCT04388501

Last Updated: 2025-03-30

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 23 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-06-07
• Study Completion Date: 2021-10-27

Brief Summary

The purpose of this study is to evaluate the potential pharmacokinetics (PK) interaction between milvexian and atorvastatin (and its metabolites) in healthy participants at steady state.

Conditions

Healthy

Study Design

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

Study Groups

Treatment Sequence ABC

Participants will receive milvexian capsule once daily (qd) for 5 days (Treatment A) in Period 1 followed by Atorvastatin tablets qd for 5 days (Treatment B) in Period 2 followed by milvexian capsules qd and atorvastatin tablets qd for 5 days (Treatment C) in Period 3. Each period is separated by a washout period of 7 days.

Group Type: EXPERIMENTAL

Milvexian

Intervention Type: DRUG

Participants will receive milvexian capsules orally qd for 5 days as per the assigned treatment sequence.

Atorvastatin

Intervention Type: DRUG

Participants will receive atorvastatin tablets orally qd for 5 days as per the assigned treatment sequence.

Treatment Sequence BCA

Participants will receive Treatment B in Period 1 followed by Treatment C in Period 2 and Treatment A in Period 3. Each Period is separated by a washout period of 7 days.

Group Type: EXPERIMENTAL

Milvexian

Intervention Type: DRUG

Participants will receive milvexian capsules orally qd for 5 days as per the assigned treatment sequence.

Atorvastatin

Intervention Type: DRUG

Participants will receive atorvastatin tablets orally qd for 5 days as per the assigned treatment sequence.

Treatment Sequence CAB

Participants will receive Treatment C in Period 1 followed by Treatment A in Period 2 and Treatment B in Period 3. Each Period is separated by a washout period of 7 days.

Group Type: EXPERIMENTAL

Milvexian

Intervention Type: DRUG

Participants will receive milvexian capsules orally qd for 5 days as per the assigned treatment sequence.

Atorvastatin

Intervention Type: DRUG

Participants will receive atorvastatin tablets orally qd for 5 days as per the assigned treatment sequence.

Treatment Sequence CBA

Participants will receive Treatment C in Period 1 followed by Treatment B in Period 2 and Treatment A in Period 3. Each Period is separated by a washout period of 7 days.

Group Type: EXPERIMENTAL

Milvexian

Intervention Type: DRUG

Participants will receive milvexian capsules orally qd for 5 days as per the assigned treatment sequence.

Atorvastatin

Intervention Type: DRUG

Participants will receive atorvastatin tablets orally qd for 5 days as per the assigned treatment sequence.

Treatment Sequence ACB

Participants will receive Treatment A in Period 1 followed by Treatment C in Period 2 and Treatment B in Period 3. Each Period is separated by a washout period of 7 days.

Group Type: EXPERIMENTAL

Milvexian

Intervention Type: DRUG

Participants will receive milvexian capsules orally qd for 5 days as per the assigned treatment sequence.

Atorvastatin

Intervention Type: DRUG

Participants will receive atorvastatin tablets orally qd for 5 days as per the assigned treatment sequence.

Treatment Sequence BAC

Participants will receive Treatment B in Period 1 followed by Treatment A in Period 2 and Treatment C in Period 3. Each Period is separated by a washout period of 7 days.

Group Type: EXPERIMENTAL

Milvexian

Intervention Type: DRUG

Participants will receive milvexian capsules orally qd for 5 days as per the assigned treatment sequence.

Atorvastatin

Intervention Type: DRUG

Participants will receive atorvastatin tablets orally qd for 5 days as per the assigned treatment sequence.

Interventions

Milvexian

Participants will receive milvexian capsules orally qd for 5 days as per the assigned treatment sequence.

Intervention Type: DRUG

Atorvastatin

Participants will receive atorvastatin tablets orally qd for 5 days as per the assigned treatment sequence.

Intervention Type: DRUG

Other Intervention Names

BMS-986177, JNJ-70033093

Eligibility Criteria

Inclusion Criteria

• Healthy on the basis of physical examination, medical history, vital signs, Electrocardiogram (ECG), and laboratory test results, including serum chemistry, blood coagulation, hematology, and urinalysis, performed at screening.
• Normal renal function at screening as evidenced by an estimated glomerular filtration rate (eGFR) of greater than or equal to (>=) 90 milliliter per minute per 1.73 square meters (mL/min/1.73 m^2) calculated with the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) formula
• Must sign an informed consent form (ICF) indicating they understand the purpose of, and procedures required for, the study and are willing to participate in the study
• If a woman, except for postmenopausal women, must have a negative highly sensitive serum (beta-human chorionic gonadotropin [beta-hCG]) at screening and urine (beta-hCG) pregnancy test on Day 1 of each treatment period
• Contraceptive use by men or women should be consistent with local regulations regarding the use of contraceptive methods for participants participating in clinical studies

Exclusion Criteria

• Participant is a woman who is pregnant, breastfeeding, or planning to become pregnant during this study or within 34 days after the last study drug administration
• History of or current clinically significant medical illness including (but not limited to) cardiac arrhythmias or other cardiac disease, hematologic disease, coagulation disorders (including any abnormal bleeding or blood dyscrasias), lipid abnormalities, significant pulmonary disease, including bronchospastic respiratory disease, gastrointestinal disease, diabetes mellitus, hepatic or renal insufficiency, thyroid disease, neurologic or psychiatric disease, infection, or any other illness that the investigator considers should exclude the participant or that could interfere with the interpretation of the study results
• Clinically significant abnormal values for hematology, coagulation, clinical chemistry (including thyroid-stimulating hormone [TSH] at screening only), or urinalysis at screening or on Day 1 prior to the first dosing, including: Hemoglobin and hematocrit less than (<) lower limit of normal; Platelet count < lower limit of normal; and activated partial thromboplastin time (aPTT) or prothrombin time (PT) greater than (>) 1.2* upper limit of normal (ULN)
• Clinically significant abnormal physical examination, vital signs, or 12 lead ECG at screening or at admission to the study center on Day 1 prior to first dosing, as deemed appropriate by the investigator
• Participants with a history of excessive menstrual bleeding

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Janssen Pharmaceutica N.V., Belgium

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Janssen Pharmaceutica N.V., Belgium Clinical Trial

Role: STUDY_DIRECTOR

Janssen Pharmaceutica N.V., Belgium

Locations

Clinical Pharmacology Unit

Merksem, , Belgium

Countries

Belgium

Other Identifiers

2019-004640-29

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

70033093THR1002

Identifier Type: OTHER

Identifier Source: secondary_id

CR108776

Identifier Type: -

Identifier Source: org_study_id