Study to Assess Bioequivalence of a New Nifurtimox Oral Tablet Formulation

Bioequivalence Clinical Trial

Official title:

Open-label, Randomized, Single-dose, Cross-over Study to Assess Bioequivalence Between a Single 120 mg Nifurtimox Tablet and a Newly Developed 120 mg Nifurtimox Tablet, Administered Orally Under Fed Conditions to Adult Male and Female Patients With Chronic Chagas' Disease

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03708133
• Other study ID #: 19500
• Status: Completed
• Phase: Phase 1
• Start date: December 5, 2018
• Est. completion date: June 18, 2019

Study information

• Verified date: June 2020
• Source: Bayer
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The primary objective of the current study is to investigate the bioequivalence of a newly developed 120 mg nifurtimox tablet formulation (Test treatment) compared with the 120 mg nifurtimox tablet currently used in the Bayer pediatric clinical development program (Reference treatment). The new tablet formulation assessed in this study is intended to replace the 120 mg nifurtimox tablet formulation currently used in clinical practice. It is an immediate-release tablet with an altered composition compared to the reference formulation. The new tablet overcomes pharmaceutical quality issues seen for the current formulation, e.g. sensitivity to humidity. Due to safety reasons, the study drug will be administered under fed conditions to adult male and female patients suffering from Chagas' disease and not healthy subjects (see also Benefit-risk assessment below).

In addition, the PK, safety, and tolerability of nifurtimox will be assessed as secondary objectives.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 24
• Est. completion date: June 18, 2019
• Est. primary completion date: April 17, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 45 Years

Eligibility

Inclusion Criteria:

• Male/female patient diagnosed with chronic Chagas' disease: Previous diagnosis of acute or chronic Chagas' disease by a health clinic prior to screening for the study. The diagnosis of chronic Chagas' disease may be made by clinical findings, supported by antibody titers if available. If there is a known history of acute disease, it is preferable to have documentation of parasites on the blood smear, if available.

• Women and men of reproductive potential must agree to use adequate contraception when sexually active. This applies for the time period between signing of the informed consent form and 12 weeks after the last administration of study drug. The definition of adequate contraception will be based on the judgment of the investigator and on local requirements. Acceptable methods of contraception include, but are not limited to: (i) condoms (male or female) with or without a spermicidal agent; (ii) diaphragm or cervical cap with spermicide; (iii) intra-uterine device; (iv) hormone-based contraception. Subjects must agree to utilize two reliable and acceptable methods of contraception simultaneously.

• Women of childbearing potential with confirmed last menstrual period by anamnesis and negative serum pregnancy test (beta-human chorionic gonadotropin [ßhCG]) at screening and negative urine pregnancy test (ßhCG) at pre-dose of each treatment.

• Women of non-childbearing potential, such as surgically sterile women with either written documentation of surgical sterility or negative serum pregnancy test (ßhCG) at screening and negative urine pregnancy test (ßhCG) at pre-dose of each treatment.

• Male subjects who agree not to act as sperm donors for 12 weeks after last administration of study drug.

• Age: 18 to 45 years (inclusive) at screening.

• Body mass index (BMI): =18 and <29.9 kg/m².

• At least 3 months since delivery or abortion, or 3 months since cessation of lactation before screening.

• Ability to understand and follow study-related instructions.

Exclusion Criteria

• Acute Chagas' disease. (During the acute phase, the parasite on a blood smear may be seen under a microscope. Different antibodies are present, depending on the course of the disease).

• Known hypersensitivity to the study drug (active substance or excipients of the preparations)

• Suspected or known porphyria.

• Clinically significant allergies (e.g. allergies affecting the lower respiratory tract such as allergic asthma or allergies requiring therapy with systemic corticosteroids) within 1 year.

• Clinically significant non-allergic drug reactions, or multiple severe drug allergies (e.g. adverse reactions in the form of bronchospasm, asthma, rhinitis or urticaria after taking non-steroidal anti-inflammatory drugs).

• Unstable or uncontrolled medical condition such as hypertension or diabetes, decompensated heart failure, GI conditions that would interfere with the absorption of the study drug (e.g. GI ulceration, peptic ulceration, GI bleeding, gastroesophageal reflux, or other GI disease affecting gastroesophageal junction), conditions that could potentially have an impact on drug metabolism or elimination (renal, hepatic such as known hepatic or biliary abnormalities), or any clinically relevant active infections in the opinion of the investigator within 4 weeks before the screening visit, e.g. clinically relevant history or presence of significant respiratory (e.g. interstitial lung disease), hematological, lymphatic, neurological, cardiovascular, psychiatric, musculoskeletal, genitourinary, immunological, metabolic (e.g. diabetes), and dermatological or connective tissue disease.

• Incompletely cured pre-existing diseases (except chronic Chagas' disease without active GI condition) for which it can be assumed that the absorption, distribution, metabolism, elimination, and effects of the study drugs will not be normal.

• Febrile illness within 1 week before the first study drug administration.

• Systolic blood pressure <100 or >140 mmHg (after resting in supine position for a minimum of 15 minutes).

• Diastolic blood pressure <50 or >90 mmHg (after resting in supine position for a minimum of 15 minutes).

• Heart rate <45

• Positive pregnancy test.

• Positive results for hepatitis B virus surface antigen (HBsAg), hepatitis C virus antibodies (anti-HCV), or human immunodeficiency virus antibodies (anti-HIV 1+2).

• Positive urine drug screening.

Related Conditions & MeSH terms

• Bioequivalence

Intervention

Drug:
• Nifurtimox (Lampit, BAYA2502)_Test
Orally intake of 1 *120mg new formulation tablet as test treatment
• Nifurtimox (Lampit, BAYA2502)_Reference
Orally intake of 1 *120mg current clinical formulation tablet as reference treatment

Locations

Country	Name	City	State
Argentina	FP Clinical Pharma	Buenos Aires	Ciudad Auton. De Buenos Aires

Sponsors (1)

Lead Sponsor	Collaborator
Bayer

Country where clinical trial is conducted

Argentina, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	AUC of nifurtimox in plasma	AUC:area under the concentration versus time curve from zero to infinity after single (first) dose	Pre-dose (up to 30 minutes before study drug administration), and at 15 minutes, 30 minutes, 45 minutes, and 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, and 15 hours post-dose
Primary	AUC(0-tlast) of nifurtimox in plasma	AUC(0-tlast): AUC from time 0 to the last data point > LLOQ(lower limit of quantitation)	Pre-dose (up to 30 minutes before study drug administration), and at 15 minutes, 30 minutes, 45 minutes, and 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, and 15 hours post-dose
Primary	Cmax of nifurtimox in plasma	Cmax: Maximum observed drug concentration in measured matrix after single dose administration	Pre-dose (up to 30 minutes before study drug administration), and at 15 minutes, 30 minutes, 45 minutes, and 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, and 15 hours post-dose
Secondary	tmax of nifurtimox in plasma	tmax: time to reach Cmax	Pre-dose (up to 30 minutes before study drug administration), and at 15 minutes, 30 minutes, 45 minutes, and 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, and 15 hours post-dose
Secondary	t1/2 of nifurtimox in plasma	t1/2: Half-life associated with terminal slope	Pre-dose (up to 30 minutes before study drug administration), and at 15 minutes, 30 minutes, 45 minutes, and 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, and 15 hours post-dose
Secondary	AUCnorm of nifurtimox in plasma	AUCnorm: AUC divided by dose per body weight	Pre-dose (up to 30 minutes before study drug administration), and at 15 minutes, 30 minutes, 45 minutes, and 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, and 15 hours post-dose
Secondary	Cmax,norm of nifurtimox in plasma	Cmax,norm: Cmax divided by dose per body weight	Pre-dose (up to 30 minutes before study drug administration), and at 15 minutes, 30 minutes, 45 minutes, and 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, and 15 hours post-dose
Secondary	Number of participants with treatment emergent adverse events		Up to 6 months

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