Pilot Pharmacokinetic Study of a Prolonged-release Formulation of St. John's Wort Extract Ze 117

Max Zeller Söhne

Status and phase: Completed; Phase 1

Conditions: Healthy

Treatments: Drug: St. John's wort film coated tablets 250 mg; Drug: St. John's wort prolonged-release tablet 500 mg

Study type: Interventional

Funder types: Industry

Identifiers

NCT02505191

Ze117-1-2014-01a

Details and patient eligibility

About

A pilot phase I, randomised, open mono-center, two parallel group clinical trial investigating the pharmacokinetics of a prolonged-release formulation in comparison to an immediate-release formulation of St. John's wort extract Ze 117 in healthy male volunteers under fasting condition.

Enrollment: 10 patients

Sex: Male

Ages: 18 to 55 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Caucasian male volunteers
• Physically and mentally healthy as judged by means of a medical and standard laboratory examination
• BMI of between 19 and 29 kg/m2, inclusively
• Weight not exceeding 90 kg
• Non-smokers (confirmed by urine cotinine test)
• Informed cConsent as documented by signature

Exclusion criteria

• Known or suspected hypersensitivity to any ingredient of the investigational medicinal product
• Any clinically significant illnesses or clinically significant surgery within 1 year prior to the administration of the study medication
• Any surgical or medical condition which might interfere with absorption, distribution, metabolism or excretion of the drug
• Any clinically significant abnormality or abnormal laboratory test results, as judged by the investigator found during the medical screening
• Positive test of hepatitis B, hepatitis C or HIV screening (HIV antibody, Hepatitis B (HBsAg), Hepatitis C (HCV)
• ECG abnormalities (clinical significant) or vital signs abnormalities (systolic blood pressure lower than 90 or over 145 mmHg, diastolic blood pressure lower than 60 or over 95 mmHg, or heart rate less than 45 or over 100bpm) at screening
• History of asthma or obstructive pulmonary disease (e.g.COPD)
• Known photohypersensitivity.
• Presents or history of alcohol dependence within the last year (> 40 g ethanol/d or more than 10 units per weeks (1unit=150 ml of wine or 360 ml of beer or 45 ml alcohol 45%))
• History of drug dependence or positive results of drug screen
• Concomitant participation in another clinical trial within the 4 weeks prior to the planned first drug administration.
• Donation of blood or blood products within 30 days prior to the planned first drug administration.
• Treatment with any medication or topical drugs with systemic action used in the past 4 weeks, prior to the planned first drug administration ,or 6 times the half-life of the respective drug, whatever is longer (excluding single use of paracetamol or ibuprofen up to 24 hours prior to the planned first drug administration).
• Suspected inability, e.g. language problems, or known or suspected non-compliance, e.g. non-willingness to fulfil the dietary restrictions
• Difficulty to swallow study medication
• Enrolment of the investigator, his/her family members, employees and other dependent persons
• Any reason which, in the opinion of the Investigator, would prevent the subject from participating the study

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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10 participants in 2 patient groups

Test

Experimental group

Description:

St. John's wort prolonged-release tablet 500 mg

Treatment:

Drug: St. John's wort prolonged-release tablet 500 mg

Reference

Active Comparator group

Description:

St. John's wort film coated tablets 250 mg (Remotiv N)

Treatment:

Drug: St. John's wort film coated tablets 250 mg