ECC5004 DDI Study With Atorvastatin, Rosuvastatin, Digoxin and Midazolam in Healthy Participants

NCT ID: NCT06293742

Last Updated: 2024-07-22

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 48 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-02-08
• Study Completion Date: 2024-04-15

Brief Summary

This is a Phase 1, open-label, non-randomized, fixed sequence study designed to evaluate the effect of ECC5004 on single dose pharmacokinetics of Atorvastatin, Rosuvastatin, Digoxin and Midazolam in healthy participants.

Detailed Description

The study consists of four parts (Part A, Part B, optional Part C and optional Part D), each with approximately 16 healthy participants enrolled. Part A and optional Part C of the study will have the same study design with two treatment periods, except that ECC5004 will be administered at a higher dose level in the optional Part C. Part B and optional Part D of the study will have the same study design with five treatment periods, except that ECC5004 will be administered at a higher dose level in optional Part D. Rosuvastatin and Digoxin will be administered alone or in combination with EC5004 in Part A and optional Part C. Atorvastatin and Midazolam will be administered alone or in combination with ECC5004 in Part B and optional Part D. The conduct of Part C and Part D with an increased dose of ECC5004 may be conducted as optional parts.

Conditions

Type 2 Diabetes Mellitus

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Digoxin, Rosuvastatin, ECC5004 (Part A)

Part A consists of 2 treatment periods. Participants will receive Digoxin and Rosuvastatin administered alone in treatment period 1 and in combination with ECC5004 in treatment period 2.

Group Type: EXPERIMENTAL

ECC5004

Intervention Type: DRUG

ECC5004 tablet will be administered orally.

Rosuvastatin

Intervention Type: DRUG

Rosuvastatin will be administered orally.

Digoxin

Intervention Type: DRUG

Digoxin will be administered orally.

Midazolam, Atorvastatin, ECC5004 (Part B)

Part B consists of 5 treatment periods. In treatment period 1, participants will receive Midazolam administered alone followed by treatment period 2 in which participants will receive Atorvastatin administered alone. In treatment period 3, participants will receive ECC5004 alone. In treatment period 4, participants will receive ECC5004 in combination with Midazolam. In treatment period 5, ECC5004 will be administered alone and co-administered with Atorvastatin.

Group Type: EXPERIMENTAL

ECC5004

Intervention Type: DRUG

ECC5004 tablet will be administered orally.

Midazolam

Intervention Type: DRUG

Midazolam will be administered orally.

Atorvastatin

Intervention Type: DRUG

Atorvastatin will be administered orally.

Digoxin, Rosuvastatin, ECC5004 (optional Part C)

Optional Part C consists of 2 treatment periods. Participants will receive Digoxin and Rosuvastatin administered alone in treatment period 1 and in combination with ECC5004 in treatment period 2.

Group Type: EXPERIMENTAL

ECC5004

Intervention Type: DRUG

ECC5004 tablet will be administered orally.

Rosuvastatin

Intervention Type: DRUG

Rosuvastatin will be administered orally.

Digoxin

Intervention Type: DRUG

Digoxin will be administered orally.

Midazolam, Atorvastatin, ECC5004 (optional Part D)

Optional Part D consists of 5 treatment periods. In treatment period 1, participants will receive Midazolam administered alone followed by treatment period 2 in which participants will receive Atorvastatin administered alone. In treatment period 3, participants will receive ECC5004 alone. In treatment period 4, participants will receive ECC5004 in combination with Midazolam. In treatment period 5, ECC5004 will be administered alone and co-administered with Atorvastatin.

Group Type: EXPERIMENTAL

ECC5004

Intervention Type: DRUG

ECC5004 tablet will be administered orally.

Midazolam

Intervention Type: DRUG

Midazolam will be administered orally.

Atorvastatin

Intervention Type: DRUG

Atorvastatin will be administered orally.

Interventions

ECC5004

ECC5004 tablet will be administered orally.

Intervention Type: DRUG

Midazolam

Midazolam will be administered orally.

Intervention Type: DRUG

Rosuvastatin

Rosuvastatin will be administered orally.

Intervention Type: DRUG

Digoxin

Digoxin will be administered orally.

Intervention Type: DRUG

Atorvastatin

Atorvastatin will be administered orally.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Male and female participants of non-childbearing potential (NCBP) between the ages of 18 to 65 years of age
• BMI of 18.0 to 32.0 kg/m2
• Female participants who are postmenopausal, confirmed by FSH test, or surgically sterile, confirmed by medical documentation, or agree to practice true abstinence
• Male participants agree to use contraception, or agree to practice true abstinence
• No clinically significant findings in physical examination, 12-lead electrocardiogram (ECG), vital sign measurements, clinical laboratory evaluations, concomitant medications, or medical/psychiatric history
• Able to understand and sign and date informed consent

Exclusion Criteria

• Females who are pregnant, planning to become pregnant, or breastfeeding during the study or within 3 months after the study
• Concomitant participation in any investigational study of any nature
• Blood loss of non-physiological reasons ≥ 200 ml (i.e., trauma, blood collection, blood donation) within 2 months prior to the first dose of study treatment, or plan to donate blood during this trial and within 1 month after the last dose of study treatment
• Serum calcitonin > 20 ng/L
• Clinically relevant acute or chronic medical conditions or diseases of the cardiovascular, gastrointestinal, hepatic, renal, endocrine, pulmonary, neurologic, psychiatric, immune or dermatologic systems
• Individual or family history of medullary thyroid carcinoma (MTC) or multiple endocrine neoplasia 2 (MEN2), or suspected MTC
• History of pancreatitis
• Significant allergic reaction to active ingredients or excipients of the study drug
• Any clinically significant abnormal findings in the participant's physical examination, laboratory tests, pregnancy test, urine drug screen, alcohol test, or medical history which in the opinion of the Investigator would prevent the participants from participating in the study
• Used or plan to use any drugs or substances that can modulate the activity of CYP3A4 within at least 14 days prior to the first dose of study treatment until after their final follow up visit
• Use of drugs with enzyme-inducing properties such as St. John's Wort within 3 weeks prior to the first dose of study treatment until after their final follow up visit

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Eccogene

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Eccogene

Role: STUDY_DIRECTOR

Eccogene Clinical Trials

Locations

Eccogene Investigational Site

Anaheim, California, United States

Countries

United States

Other Identifiers

EC0007

Identifier Type: -

Identifier Source: org_study_id