Pharmacokinetic and Placental Transfer of Levetiracetam

Epilepsy in Pregnancy Clinical Trial

— EPICEINTE  

Official title:

Study of Maternal Pharmacokinetic and Placental Transfer of Levetiracetam

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04117425
• Other study ID #: CRC17036
• Status: Recruiting
• Phase: N/A
• Start date: April 20, 2022
• Est. completion date: September 2023

Study information

• Verified date: September 2022
• Source: Assistance Publique - Hôpitaux de Paris
• Contact: Deborah Hirt, PhD
• Phone: +33 1 58 41 32 83
• Email: deborah.hirt[@]aphp.fr
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Hypotheses: The treatment of epilepsy during pregnancy is difficult because of the risk of anti-epileptic drugs on the one hand and the risk of destabilization of epilepsy in the mother on the other hand. There is limited data on the pharmacokinetics (concentration study) and pharmacodynamics (efficacy and toxicity effects study) of levetiracetam in pregnant women. The few studies focus on few women and show very strong interindividual variability and a tendency to decrease total concentrations.

Main objective: To develop a population pharmacokinetic model of levetiracetam during pregnancy. After the study, this model could be used to propose dose adjustments to maintain stable concentrations in pregnant women throughout pregnancy.

Secondary objectives:

• Describe placental transfer during childbirth and during a medical termination of pregnancy

• Link the concentration and its variation in the individual to the effects of treatment

Description:

Methodology: Are included by the neurology service, pregnant women which are already under levetiracetam and / or obstetric gynecology services for her treatment of epilepsy, pregnant women at first consultation. Women are already taking levetiracetam and the drug is not provided by the study40 mother-child couples, as well as 10 women who undergo a medical termination of pregnancy will have to be included in the study, in 7 maternities in Paris.

Women are already taking the drugs, according to the practices of the different services, and the study will not change their prescriptions of these drugs. The women will have a blood sample at 3 visits during pregnancy (11-14 weeks, 24-28 weeks and 35-39 weeks) and at the post-partum consultation. At delivery, a collection of the mother, cord blood and amniotic fluid will be performed. A salivary specimen will be routinely collected at the same time as the mother's plasma sample.

The pharmaco-statistical analysis will be conducted using non-linear mixed-effect modeling programs (Monolix and Nonmem) to calculate the main pharmacokinetic parameters of the mother and fetus and to estimate their variability. This type of modeling makes it possible to take into account individual covariates (weight, gestational age ...) to explain the pharmacokinetic variability between mother - child pairs. The final model will be validated by a simulation technique. The final model will be used to rationalize the changes in antiepileptic doses during pregnancy and to explain the differences in passage, based on individual covariates, then to perform simulations to find out how to modify the administration for treatment to be effective as often as possible.

The secondary endpoints are

• Exposure ratio (area under the concentration-time curve) between the mother and the fetus to describe the transplacental passage of levetiracetam levetiracetam.

• To correlate the evolution of the concentrations in the woman (value in the woman whose treatment is balanced before the pregnancy minus the value when she is pregnant) to

• the effectiveness (number of crises that the patient did).

• tolerance: presence or absence of clinical and biological abnormalities occurring in pregnant women and children

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 50
• Est. completion date: September 2023
• Est. primary completion date: June 2023
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• pregnant Women of childbearing age who are pregnant

• Age =18 years

• Women with epilepsy treated with levetiracetam in monotherapy or combination

• affiliated to a social security scheme (or entitled)

Exclusion Criteria:

• Women treated with antiepileptics for pathology other than epilepsy

• Women treated with a combination of more than 3 antiepileptics

• Severe anemia

• Renal failure (moderate to severe)

• Hepatic impairment (moderate to severe)

• Alcohol and/or recreational drug use

• Trend towards non-compliance with treatment

• Inability to maintain a Crisis Observation Workbook

• Suicidal Ideas

• Uncontrolled thyroid disease

Related Conditions & MeSH terms

• Epilepsy
• Epilepsy in Pregnancy

Intervention

Biological:
• biological collection
Blood collection at each trimester of pregnancy, delivery and post partum visit or at medical interruption. Collection of saliva at each trimester of pregnancy and post partum visit. Collection of cord blood and amniotic fluid at delivery or at medical interruption.

Locations

Country	Name	City	State
France	hospital Cochin	Paris

Sponsors (1)

Lead Sponsor	Collaborator
Assistance Publique - Hôpitaux de Paris

Country where clinical trial is conducted

France, 

References & Publications (3)

Pennell PB. Antiepileptic drug pharmacokinetics during pregnancy and lactation. Neurology. 2003 Sep 1;61(6 Suppl 2):S35-42. Review. — View Citation

Tomson T, Palm R, Källén K, Ben-Menachem E, Söderfeldt B, Danielsson B, Johansson R, Luef G, Ohman I. Pharmacokinetics of levetiracetam during pregnancy, delivery, in the neonatal period, and lactation. Epilepsia. 2007 Jun;48(6):1111-6. Epub 2007 Mar 22. — View Citation

Westin AA, Reimers A, Helde G, Nakken KO, Brodtkorb E. Serum concentration/dose ratio of levetiracetam before, during and after pregnancy. Seizure. 2008 Mar;17(2):192-8. doi: 10.1016/j.seizure.2007.11.027. Epub 2008 Jan 3. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Levetiracetam pharmacokinetics in pregnancy	Levetiracetam concentrations as a function of time	At delivery
Secondary	Levetiracetam pharmacokinetics in pregnancy	Levetiracetam concentrations as a function of time	At inclusion
Secondary	Levetiracetam pharmacokinetics in pregnancy	Levetiracetam concentrations as a function of time	Until 17 weeks
Secondary	Levetiracetam pharmacokinetics in pregnancy	Levetiracetam concentrations as a function of time	Until 28 weeks
Secondary	Levetiracetam pharmacokinetics in pregnancy	Levetiracetam concentrations as a function of time	Until 6 week after delivery
Secondary	Exposure ratio	area below the concentration curve as a function of time) between the mother and the fetus to describe the transplacental passage of levetiracetam.	At delivery
Secondary	Link between levetiracetam concentrations and effects	correlate the evolution of the concentrations in the woman (value in the woman whose treatment is balanced before the pregnancy minus the value when she is pregnant) to; the effectiveness (number of crises that the patient did).; tolerance: presence or absence of clinical and biological abnormalities occurring in pregnant women and children.	At inclusion
Secondary	Link between levetiracetam concentrations and effects	Correlate the evolution of the concentrations in the woman (value in the woman whose treatment is balanced before the pregnancy minus the value when she is pregnant) to; the effectiveness (number of crises that the patient did).; tolerance: presence or absence of clinical and biological abnormalities occurring in pregnant women and children	Until 17 weeks
Secondary	Link between levetiracetam concentrations and effects	Correlate the evolution of the concentrations in the woman (value in the woman whose treatment is balanced before the pregnancy minus the value when she is pregnant) to; the effectiveness (number of crises that the patient did).; tolerance: presence or absence of clinical and biological abnormalities occurring in pregnant women and children	Until 28 weeks
Secondary	Link between levetiracetam concentrations and effects	Correlate the evolution of the concentrations in the woman (value in the woman whose treatment is balanced before the pregnancy minus the value when she is pregnant) to; the effectiveness (number of crises that the patient did).; tolerance: presence or absence of clinical and biological abnormalities occurring in pregnant women and children.	Until 6 week after delivery