Bioequivalence Study With Pharmacokinetic Endpoints, Comparing a Single Dose of Iron Sucrose Azad Injection of Azad Pharma Corporation (AG), With a Single Dose of Venofer® Injection of Vifor Corporation (AG) in Healthy Adult Volunteers

Azad Pharma

Status and phase

Completed

Phase 1

Conditions

Healthy Volunteers

Treatments

Drug: Iron Sucrose Azad

Drug: Venofer®

Study type

Interventional

Funder types

Industry

Identifiers

NCT02391181

AZAD-BE01

Details and patient eligibility

About

A Clinical Trial to Demonstrate the Comparability of the Two Iron Sucrose Injection Solutions Iron Sucrose Azad of Azad Pharma AG and Venofer® of Vifor Pharma AG. The Hypothesis is That Both Iron Sucrose Injection Solutions Reveal the Same Active Substance Availability in the Blood Circuit.

Full description

A single dose 100mg Iron Sucrose Azad (5 mL single dose vial, each mL containing 20 mg/mL elemental iron as iron sucrose in water for injection) of Azad Pharma AG or a single dose 100mg Venofer® (5 mL single dose vial, iron sucrose injection, United States Pharmacopeia (USP), 20 mg/mL) will be administered to healthy adult volunteers in a crossover-design. The assignment to either test or reference product in the crossover design is based on a randomization schedule. A wash-out period of at least 5 half-lives of iron sucrose was calculated in this crossover design which accounts an overall study duration of at least 10 days (max 19 days) for each volunteer. Overall the study participant has to attend the clinical site for 5 active study days.

The study follows the recommended format outlined 2013 by the European Medicines Agency (EMA), i.e. single-dose with primary variables being AUC and Cmax of baseline corrected total- and transferrin-bound serum iron. In addition baseline non-corrected values will be analysed due to the known variability in baseline iron levels (both intra- and inter-individual).

The assays for total- and transferrin-bound serum iron will be validated, in order to ensure dependable readouts as recommended by EMA.

Enrollment

30 patients

Sex

All

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Male and female healthy volunteers within the age range of 18 to 45 years (both inclusive)
Comprehension of the nature and purpose of the study and willingness to comply with the requirements of the entire procedure
Subjects of good health based on previous medical history, physical examination, vital signs, electrocardiogram (ECG), and clinical laboratory tests assessed at the time of screening.
Ferritin levels ≥ 30 µg/l for female and male subjects
Transferrin ≥ 200 mg/dl for female and male subjects
Hemoglobin levels ≥ 12 g/dl for female subjects and ≥ 13.5 g/dl for male subjects
Females of childbearing potential must provide a negative urine pregnancy test at time of screening and have to be compliant with effective hormonal form of birth control throughout the whole study

Exclusion criteria

Subjects with a BMI of < 19 kg/m2 and > 30 kg/m2
Pregnancy (as determined by a positive urine pregnancy test at the screening or prior each crossover phase) or breast feeding
Females with history of hypermenorrhea or menorrhagia
Females with history of myoma, endometriosis or uterus hypoplasia or any other gynecological disorder
History of iron deficiency within six months prior screening
History of anemia within 1 year prior screening
Presence of iron overload or disturbances in utilization of iron
History or evidence of allergy or hypersensitivity to the active substance Iron Sucrose of both test and reference product, the finished test and reference product or any of its excipients (water for injection, sodium hydroxide)
Hypersensitivity to other parenteral iron products
Use of iron supplements or iron containing herbal or nutritional supplements within last three months prior to start of the study
History of difficulty with donating blood or difficulty in accessibility of veins in left and right arm
Donation of blood (one unit or 350 mL) within last three months prior first dose administration of the study drug
Evidence of an active or suspected cancer, or a history of malignancy within the last 2 years, with the exception of patients with basal cell carcinoma that has been excised and cured
History of any systemic anti-neoplastic or immunomodulatory treatment (including supraphysiologic doses of steroids and radiation) 6 months prior to the first dose of study drug or the expectation that such treatment will be needed at any time during the study
History of bleeding disorders or anticoagulant use
History or other evidence of chronic pulmonary or cardiovascular disease associated with functional limitation
History of uncontrolled severe seizure disorder.
Any signs of acute infection or inflammation.
History or other evidence of severe illness, or any other condition which would make the subject in the opinion of the investigator, unsuitable for the study
Any clinically significant abnormal laboratory values on the laboratory evaluations, medical history or physical examination at the screening
Positive Human Immunodeficiency Virus (HIV)/ Hepatitis B Virus (HBV)/ hepatitis C virus (HCV) serology tests at the time of the screening visit
Abnormal 12-lead ECG at the time of screening that is considered to be clinically significant
History or presence of severe or medical treated allergies or immune or inflammatory conditions (eg. systemic lupus erythematosus, rheumatoid arthritis)
History of atopic allergy associated with severe asthma
Recent history or ongoing kidney or liver dysfunction
Any other major illness in last three months or any significant ongoing chronic medical illness
Subjects who regularly use more than 2 units of alcohol per day (one unit of alcohol equals ½ liter of beer, 200mL wine or 50mL of spirits)or there is evidence of Cocaine, Amphetamines, Metformin, Tetrahydrocannabinol (THC), Methadone, 3,4-Methylendioxy-N-Methylamphetamin (MDMA), Morphine, Barbiturates, Benzodiazepines and Tricyclic antidepressants in urine at the screening)
Heavy smokers (> 10 cigarettes/day) in the last three months prior to start of the study
Any concomitant medication (except paracetamol and contraceptives) within the last two weeks, including over-the-counter and herbal products, prior to receiving the dose of study medication
Participation in any clinical trial within last one months
Subjects who are considered by the investigator to be non-compliant or unlikely to complete the study.