Multiple Sclerosis (MS)
Conditions
Brief summary
Observational data have suggested no increased risk of adverse pregnancy outcomes associated with exposure to interferon-beta (IFNB) before or during pregnancy. After the emergence of these data, the European Medicines Agency approved a label change for IFNB in September 2019, stating that use of IFNB during pregnancy may be considered, if clinically needed. However, limited data on pregnancies exposed in the 2nd and 3rd trimesters were observed. INFORM is a secondary use of data drug utilisation study (DUS) to determine late pregnancy exposure (i.e. during the 2nd and 3rd trimester) to IFNB in Finland and Sweden, which will inform whether the number of exposed pregnancies is adequate to conduct a cohort study on adverse pregnancy outcomes, with a focus on late pregnancy exposure. The number of pregnancies will be initially reported three years after the revised label implementation (September 2019) and will include data on pregnancies from 1996 in Finland and from 2005 in Sweden up through 31 December 2022. If the number of pregnancies is deemed adequate for conducting the cohort study on adverse pregnancy outcomes, this DUS will be finalised with the drug utilisation data accrued up through 31 December 2022. If the number of pregnancies until 31 December 2022 is deemed inadequate, this study may be continued and the primary and secondary objectives may be examined five years after the revised label implementation, including pregnancies until 31 December 2024.
Interventions
DRUGAvonex (IFNβ-1-a, Biogen Netherlands B.V)
Information on drug use in hospitals and outpatient clinics are not recorded in the drug registers used in the study and, thus, information on exposure to these medications is not available.
DRUGRebif (IFNβ-1-a, Merck Europe B.V.)
Information on drug use in hospitals and outpatient clinics are not recorded in the drug registers used in the study and, thus, information on exposure to these medications is not available.
DRUGExtavia (IFNβ-1-b, Novartis Europharm Limited)
Information on drug use in hospitals and outpatient clinics are not recorded in the drug registers used in the study and, thus, information on exposure to these medications is not available.
DRUGBetaseron (IFN-β-1-b, BAY86-5046, Bayer AG)
Information on drug use in hospitals and outpatient clinics are not recorded in the drug registers used in the study and, thus, information on exposure to these medications is not available.
DRUGPlegridy (Peg IFNβ-1-a, Biogen Netherlands B.V)
Information on drug use in hospitals and outpatient clinics are not recorded in the drug registers used in the study and, thus, information on exposure to these medications is not available.
DRUGMS disease modifying drugs (MSDMDs)
Information on drug use in hospitals and outpatient clinics are not recorded in the drug registers used in the study and, thus, information on exposure to these medications is not available.
Sponsors
Bayer
Biogen Netherlands B.V
Novartis Europharm Limited
Merck Europe B.V.
Study design
Observational model
COHORT
Time perspective
OTHER
Eligibility
Sex/Gender
FEMALE
Age
12 Years to 64 Years
Healthy volunteers
No
Inclusion criteria
* Women with a diagnosis of MS disease, regardless of MS clinical type, recorded at least once during the full study period. * Women with at least one recorded pregnancy after the MS diagnosis (including pregnancies ending in live birth, stillbirth, spontaneous abortion, ectopic pregnancy, or elective termination)
Exclusion criteria
\- None.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The number of pregnancies of women with MS, not allowing exposure to other MS Disease Modifying Drugs (MSDMDs) | Data recorded between 01 January 1996 - 31 December 2022 in Finland, and 01 July 2005 - 31 December 2022 in Sweden. | Analysis groups: Pregnancies exposed to IFNB only group and Pregnancies unexposed to IFNB nor other MSDMDs group |
| The level of precision for the risk of pre-defined adverse pregnancy outcomes in late pregnancy that can be obtained with the available number of exposed and unexposed pregnancies | Data recorded between 01 January 1996 - 31 December 2022 in Finland, and 01 July 2005 - 31 December 2022 in Sweden. | Pre-defined adverse pregnancy outcomes: * Anomalies: Major congenital anomalies (MCA); All anomalies, including minor and major * Fatal outcomes: Spontaneous abortions, Elective terminations, Stillbirth and Neonatal mortality * Growth outcomes: Small for gestation age and Low birth weight * Other outcomes: Preterm birth Late pregnancy, i.e. the 2nd and 3rd trimester. |
| The annual number of pregnancies of women with MS in the exposure groups | Data recorded between 2015-2019 and 2020-2022. | Analysis in Pregnancies exposed to IFNB only group. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| The number of pregnancies of women with MS in Finland and Sweden in exposure groups allowing exposure to other MSDMDs | Data recorded between 01 January 1996 - 31 December 2022 in Finland, and 01 July 2005 - 31 December 2022 in Sweden. | Analysis groups: Pregnancies exposed to IFNB (regardless of other MSDMDs) group and Pregnancies unexposed to IFNB (regardless of other MSDMDs) group |
| The annual number of women with MS in childbearing age, and with dispensed IFNB | Data recorded between 2015 to 2022 in Finland and Sweden | — |
Countries
Finland, Sweden
Outcome results
None listed