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Assessment of the Pharmacodynamic Effect on Plasma Folate and Red Blood Cell Folate and Comparison of the Folate Metabolites During the 24 Weeks of Treatment (Yasmin + Metafolin Versus Yasmin + Folic Acid) Followed by a 20 Week Elimination Phase of Folate

Information source: Bayer
ClinicalTrials.gov processed this data on August 23, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Contraception

Intervention: EE 0.03 mg/DRSP 3 mg/Metafolin + folic acid placebo (Drug); EE 0.03 mg/DRSP 3 mg (Yasmin) + folic acid (Drug)

Phase: Phase 1

Status: Completed

Sponsored by: Bayer

Official(s) and/or principal investigator(s):
Bayer Study Director, Study Director, Affiliation: Bayer

Summary

The purpose of this study is to examine and compare the uptake of levomefolate calcium (Metafolin, a registered vitamin supplement) and folic acid in the body during 24 weeks of treatment with a following folate elimination phase of 20 weeks in healthy volunteers seeking contraception. Yasmin (oral contraceptive containing drospirenone and ethinylestradiol) was co-administered over the entire period of 44 weeks.

Clinical Details

Official title: A Randomized, Double-blind, Double-dummy, 2-parallel Arms Clinical Trial to Assess the Pharmacodynamic Effect on Plasma Folate and Red Blood Cell Folate and to Compare the Profile of Circulating Folate Metabolites During 24 Weeks of Treatment With an Oral Contraceptive Containing Ethinylestradiol, Drospirenone and L-5-methyltetrahydrofolate (SH T04532A and SH T04532C) or Yasmin (SH T04532D and SH T04532PC) Co-administered With Folic Acid (SH K04532B) Followed by 20 Weeks of Open-label Treatment With Yasmin Only (Folate Elimination Phase) in Women Seeking Contraception

Study design: Allocation: Randomized, Endpoint Classification: Pharmacodynamics Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Primary outcome:

Area Under the Curve (AUC) From Time 0 to 24 Weeks [AUC(0-24weeks)] for Plasma Folate and RBC (Red Blood Cell) Folate (Baseline Uncorrected)

Area Under the Curve From Time 0 to 24 Weeks [AUC(0-24weeks)] for Plasma Folate and RBC (Red Blood Cell) Folate (Baseline Corrected)

Proportion of Participants With RBC Folate Below 906 Nmol/L in the Yasmin + Metafolin Group in the Folate Elimination Phase (Week 24 to 44)

Secondary outcome:

Folate Metabolite Pattern in Plasma at Baseline

Folate Metabolite Pattern in Plasma at Cycle 3

Folate Metabolite Pattern in Plasma at Cycle 6

Homocysteine Concentrations in Plasma at Baseline and at the End of Treatment (Week 24) With Metafolin

Homocysteine Concentrations in Plasma at Baseline and at the End of Treatment (Week 24) With Folic Acid

Eligibility

Minimum age: 18 Years. Maximum age: 40 Years. Gender(s): Female.

Criteria:

Inclusion Criteria:

- Age 18-40 years.

- RBC folate > 317 nmol/L and < 906 nmol/L.

- At least 1 menstruation during the last 3 months before screening with the exception

of women using progestin-only methods (injection, implant) or progestin-releasing intrauterine system (IUS).

- Negative pregnancy test at screening and at admission into the study.

- Healthy as confirmed by medical history and physical examination.

- Body mass index (BMI) of 18. 5-30. 0 kg/m2 .

- Volunteers that smoke less than 10 cigarettes per day can be included up to the age

of 30 years.

- Adequate vitamin B12 status defined as plasma B12 concentrations ≥ 110 pmol/L.

Exclusion Criteria:

- Regular intake of folic acid defined as > 100 μg folic acid/day in vitamin

supplements or fortified food during the last 4 months.

- Treatment with the following medications, which has the potential of interfering with

folate metabolism: cholestyramine, methotrexate, trimethoprim, sulfasalazine, salicylic acid, cotrimoxazol, antacids or antiepileptic drugs.

- Pregnancy, lactation (at least three cycles have to follow delivery, abortion, or

lactation before start of treatment)

- Vascular or metabolic disease including existing or previous arterial thromboembolic

diseases (myocardial infarction, stroke), existing or previous venous thromboembolic diseases (deep vein thrombosis, pulmonary embolism), and any condition which could increase the risk to suffer any of the above mentioned disorders

- Any disease or condition that could compromise the function of the body systems and

could result in altered absorption, excessive accumulation, impaired metabolism, or altered excretion of the study medication.

- Any disease that may worsen under hormonal treatment or might interfere with the

conduct of the study or the interpretation of the results (e. g., herpes gestationis or idiopathic icterus pregnancy; middle-ear deafness ; Sydenham's chorea, porphyria, disturbances in the bile flow.

- Liver diseases: Presence or history of severe hepatic diseases including benign or

malignant tumors

Locations and Contacts

Nuvisan GmbH, Neu-Ulm, Bayern 89231, Germany
Additional Information

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Starting date: December 2006
Last updated: September 15, 2013

Page last updated: August 23, 2015

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