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Completed

NCT Number: NCT03892213

Pharmacokinetic Drug-Drug Interaction Study

The purpose of this study is to determine whether benznidazole and E1224 should be administered concomitantly in patients with Chagas Disease as not enough data are available. This study aims to assess cross interactions of these two compounds.

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Key information

Age range

18 year–45 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Primary location

FP Clinical Pharma - Juncal 4484 - 3o piso

Buenos Aires, C1425BAB, Argentina

About this study

Benznidazole and E1224 are intended to be administered concomitantly in patients with Chagas disease. Thus, an in vivo interaction study in healthy volunteers may be justified as the two drugs are intended to be administered concomitantly in patients and no in vivo nor in vitro data are available.

In addition both interactions (potential for benznidazole to interact on the pharmacokinetic (PK) of E1224 and potential for E1224 on the PK of benznidazole should be studied.

Benznidazole t1/2 is quite short (12 h) whereas E1224 t1/2 is very long (more than 200 h). Therefore it was chosen to study the interaction of E1224 at steady-state while interaction of benznidazole after single dose appears more appropriate instead of a classical randomized cross-over design.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male healthy volunteers 18 to 45 years of age;
  • Light smokers (less than 5 cigarettes per day) or subjects who are non-smokers;
  • Male subjects with a body weight of at least 50 kg and a body mass index (BMI) calculated as weight in kg/height (in m2) from 18 to 28 kg/m2 at screening;
  • Able to communicate well with the Investigator and research staff and to comply with the requirements of the entire study;
  • Provision of written informed consent to participate as shown by a signature on the volunteer consent form;

Exclusion criteria

  • Who on direct questioning and physical examination have evidence of any clinically significant acute or chronic disease, including known or suspected HIV, hepatites B virus (HBV) or hepatites C virus (HCV) infection;
  • Who has positive diagnosis of T. cruzi infection indicated by Conventional serology;
  • With any clinically significant abnormality following review of pre-study laboratory tests, vital signs, full physical examination and 12-lead ECG;
  • Who forfeit their freedom by administrative or legal award or who were under guardianship;
  • Unwilling to give their informed consent;
  • Who have a positive laboratory test for Hepatitis B surface antigen (HbsAg), or anti-HIV 1/2 or anti- HCV antibodies;
  • Who have a history of allergy (serious or not), allergic skin rash, asthma, intolerance, sensitivity or photosensitivity to any drug;
  • Who are known or suspected alcohol or drug abusers (more than 14 units of alcohol per week, one unit = 8 g or about 10 mL of pure alcohol);

Treatment and study plan

Benznidazole

Drug

Benznidazole single dose (2.5 mg/kg) at Day 1. Benznidazole single dose (2.5 mg/kg) at Day 9*. Benznidazole multiple dose (2.5 mg/kg twice daily) from Day 12* until Day 15.

Other names: Abarax® (Benznidazole 100mg or 50mg).

E1224

Drug

E1224 multiple dose 400 mg loading dose once daily for 3 days (i.e. from Day 4 to Day 6 followed by maintenance dose 100mg once daily for 9 days (from Day 7 to Day15).

On Day 9 and from Day 12 to Day 15, E1224 and benznidazole will be given concomitantly.

Other names: E1224 is a prodrug monolysine form of ravuconazole.

Primary outcomes

  1. Maximum serum concentration (Cmax) of Benznidazole

    Time frame: Day 1 and day 9

    BNZ PK parameter following single dose to investigate the possible drug-drug interaction between BNZ and E1224 through evaluation of the PK characteristics of both drugs when given alone or concomitantly.

  2. Time of occurrence of maximum plasma concentration (tmax) of Benznidazole

    Time frame: Day 1 and day 9

    BNZ PK parameter following single dose to investigate the possible drug-drug interaction between BNZ and E1224 through evaluation of the PK characteristics of both drugs when given alone or concomitantly.

  3. Area under the serum concentration versus time curve from time zero to the time (t) corresponding to the last quantifiable concentration (AUC 0-t) of Benznidazole

    Time frame: Day 1 and day 9

    BNZ PK parameter following single dose to investigate the possible drug-drug interaction between BNZ and E1224 through evaluation of the PK characteristics of both drugs when given alone or concomitantly.

  4. Area under the concentration-time curve from time zero to infinity with extrapolation of the terminal phase (AUC 0-∞) of Benznidazole

    Time frame: Day 1 and day 9

    BNZ PK parameter following single dose to investigate the possible drug-drug interaction between BNZ and E1224 through evaluation of the PK characteristics of both drugs when given alone or concomitantly.

  5. Terminal half-life (t1/2) of Benznidazole

    Time frame: Day 1 and day 9

    BNZ PK parameter following single dose to investigate the possible drug-drug interaction between BNZ and E1224 through evaluation of the PK characteristics of both drugs when given alone or concomitantly.

  6. Maximum serum concentration (Cmax) of Ravuconazole.

    Time frame: Day 8 and day 15, day 6 (morning pre-dose), day 7 (morning pre-dose), day 8 (morning pre-dose), day 13 (morning pre-dose), day 14 (morning pre-dose), and day 15 (morning pre-dose)

    PK parameter of ravuconazole following multiple dose to investigate the possible drug-drug interaction between BNZ and E1224 (prodrug of ravuconazole) through evaluation of the PK characteristics of both drugs when given alone or concomitantly.

  7. Time of occurrence of maximum plasma concentration (tmax) of Ravuconazole.

    Time frame: Day 8 and day 15, day 6 (morning pre-dose), day 7 (morning pre-dose), day 8 (morning pre-dose), day 13 (morning pre-dose), day 14 (morning pre-dose), and day 15 (morning pre-dose)

    PK parameter of ravuconazole following multiple dose to investigate the possible drug-drug interaction between BNZ and E1224 (prodrug of ravuconazole) through evaluation of the PK characteristics of both drugs when given alone or concomitantly.

  8. The area under the blood drug concentration vs. time curve from time zero (pre-dose) to 24 h post-dose (AUC 0-24)

    Time frame: Day 8 and day 15, day 6 (morning pre-dose), day 7 (morning pre-dose), day 8 (morning pre-dose), day 13 (morning pre-dose), day 14 (morning pre-dose), and day 15 (morning pre-dose)

    PK parameter of ravuconazole following multiple dose to investigate the possible drug-drug interaction between BNZ and E1224 (prodrug of ravuconazole) through evaluation of the PK characteristics of both drugs when given alone or concomitantly.

Secondary outcomes

  1. Incidence of Adverse Events (AEs)

    Time frame: Through study completion, i.e up to 22 days.

    Monitoring for the occurrence of adverse events (AEs)

  2. Clinically significant alterations in pulse rate

    Time frame: Through study completion, i.e up to 22 days.

    Parameter to assess the safety and tolerability of multiple oral doses of BNZ and E1224 given in healthy male subjects.

  3. Clinically significant alterations in blood pressure

    Time frame: Through study completion, i.e up to 22 days.

    Parameter to assess the safety and tolerability of multiple oral doses of BNZ and E1224 given in healthy male subjects.

  4. Clinically significant alterations in 12-lead ECG

    Time frame: Through study completion, i.e up to 22 days.

    Parameter to assess the safety and tolerability of multiple oral doses of BNZ and E1224 given in healthy male subjects

  5. Clinically significant Haematology abnormalities (hemoglobin, RBC, hematocrit, MCV, MCH, MCHC, WBC, including differential, platelet counts)

    Time frame: Day 1, Day 4, Day 7, Day 9, Day 10, Day 12, Day 13, Day 14 and Day 15 pre morning dose

    Parameter to assess the safety and tolerability of multiple oral doses of BNZ and E1224 given in healthy male subjects.

  6. Clinically significant Biochemistry abnormalities (albumin (ALB), ALP, ALT, AST, gamma-glutamyl transferase (GGT), chlorides (Cl-), creatinine, glucose (GLU), potassium (K+), sodium (Na+), total bilirubin (TBIL), total proteins (TP), Urea.

    Time frame: Day 1, Day 4, Day 7, Day 9, Day 10, Day 12, Day 13, Day 14 and Day 15 pre morning dose

    Parameter to assess the safety and tolerability of multiple oral doses of BNZ and E1224 given in healthy male subjects.

  7. Clinically significant Urinalysis abnormalities (leukocytes, pH, proteins, urobilinogen, blood, nitrites, glucose, ketone bodies, bilirubin).

    Time frame: Screening and day 22

    Parameter to assess the safety and tolerability of multiple oral doses of BNZ and E1224 given in healthy male subjects.

Sponsors and collaborators

Lead sponsor

Drugs for Neglected Diseases

Other

Collaborators

  • PhinC Development

Registry information

Official study title

A Phase 1 Pharmacokinetic Drug-Drug Interaction Study of Benznidazole and E1224 in Healthy Male Volunteers

Important dates

Study start
2014
Primary completion
2014
Study completion
2015
First posted
Mar 27, 2019
Registry last updated
Mar 27, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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