Pharmacokinetics and Safety of AmBisome and DKF-5122

NCT ID: NCT05749380

Last Updated: 2023-03-01

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 38 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-09-07
• Study Completion Date: 2022-01-28

Brief Summary

The purpose of the study is to assess the Safety and Pharmacokinetic Characteristics of AmBisome and DKF-5122

Conditions

Invasive Fungal Infections; Neutropenic Fever

Study Design

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

Study Groups

1A(RT)

Patients (AmBisome, DKF-5122)

Group Type: OTHER

AmBisome

Intervention Type: DRUG

Reference, dose of 3 mg/kg.

DKF-5122

Intervention Type: DRUG

Test, dose of 3 mg/kg

1B(TR)

Patients (DKF-5122, AmBisome)

Group Type: OTHER

AmBisome

Intervention Type: DRUG

Reference, dose of 3 mg/kg.

DKF-5122

Intervention Type: DRUG

Test, dose of 3 mg/kg

2A(RT)

Healthy subjects (AmBisome, DKF-5122)

Group Type: OTHER

AmBisome

Intervention Type: DRUG

Reference, dose of 3 mg/kg.

DKF-5122

Intervention Type: DRUG

Test, dose of 3 mg/kg

2B(TR)

Healthy subjects (DKF-5122, AmBisome)

Group Type: OTHER

AmBisome

Intervention Type: DRUG

Reference, dose of 3 mg/kg.

DKF-5122

Intervention Type: DRUG

Test, dose of 3 mg/kg

Interventions

AmBisome

Reference, dose of 3 mg/kg.

Intervention Type: DRUG

DKF-5122

Test, dose of 3 mg/kg

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Part 1. Patients

1. Age 19 years and older

2. Empirical therapy for presumed fungal infection in febrile, neutropenic patients

3. Voluntarily decided to participate in the study and signed the informed consent form

4. Having contraception during the study

• Part 2. Healthy subjects

1. Age 19 to 45 years

2. Body weight 55 kg or more, within ±20% of the ideal body weight

3. Having no congenital or chronic disease within the last 5 years.

4. Voluntarily decided to participate in the study and signed the informed consent form

5. Having contraception during the study

Exclusion Criteria

• Part 1. Patients

1. Clinically significant conditions that may affect the pharmacokinetics of amphotericin

2. History of diseases that may affect the pharmacokinetics of amphotericin

3. History of drug abuse

4. History of hypersensitivity to ingredients of investigational products

5. Unable to maintain proper contraception

6. Pregnant or breast-feeding

7. The following laboratory test results at screening

• Hemoglobin < 8.0 g/dL
• Serum Creatinine > 2x the UNL
• AST or ALT > 10x UNL
• Systolic blood pressure ≥ 140 mmHg or ≤ 90 mmHg
• Diastolic blood pressure ≥ 90 mmHg or ≤ 60 mmHg

8. Before the first administration of investigational products

• Participation to other clinical trials within 6 months
• Whole blood donation within 60 days or component within 30 days
• (Herbal) medicines that may affect the pharmacokinetics of amphotericin within 14 days
• Grapefruit-containing foods within 7 days
• Excessive exercise within 7 days

9. Excessive caffeine and alcohol consumption, or a smoker

10. Not eligible due to other reasons at the investigator's discretion

• Part 2. Healthy subjects

1. Clinically significant disorders or a medical history of active cardiovascular, respiratory , kidney, endocrine, hematological, digestive, central nervous system, psychiatric disease, or malignant tumor

2. Clinically significant conditions that may affect the pharmacokinetics of amphotericin

3. History of diseases that may affect the pharmacokinetics of amphotericin

4. History of drug abuse

5. History of hypersensitivity to ingredients of investigational products

6. Unable to maintain proper contraception

7. Pregnant or breast-feeding

8. The following laboratory test results at screening

• Hemoglobin < 13.0 g/dL
• Serum Creatinine > 1.25 x UNL
• eGFR < 90 mL/min/1.73 m2
• AST or ALT > 1.25 x UNL
• Total bilirubin > 1.25 x UNL
• CPK > 1.5 x UNL
• Systolic blood pressure ≥140 mmHg or ≤90 mmHg
• Diastolic blood pressure ≥ 90 mmHg or ≤60 mmHg
• Arrhythmia

9. Before the first administration of investigational products

• Participation to other clinical trials within 6 months
• Whole blood donation within 60 days or component within 30 days
• Drugs that induce or inhibit drug metabolism enzymes within 30 days
• Vaccination within 7 days
• Prescription drugs, herbal medicines, over-the-counters, or vitamins within 14 days
• Grapefruit-containing foods within 7 days
• Excessive exercise within 7 days

10. Excessive caffeine and alcohol consumption, or a smoker

11. Not eligible due to other reasons at the investigator's discretion

• Minimum Eligible Age: 19 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Dongkook Pharmaceutical Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

The Catholic University of Korea Seoul St. Mary's Hospital

Seoul, Seocho-gu, South Korea

Countries

South Korea

Other Identifiers

DKF-5122-BE

Identifier Type: -

Identifier Source: org_study_id