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NCT07844070Active, not recruiting

A Study of Disease Modifying Therapy Use in Women With Multiple Sclerosis Before, During, and After Pregnancy

Disease Modifying Therapy Use in Women With Multiple Sclerosis Before, During, and After Pregnancy

Source: ClinicalTrials.gov · Last updated 28 Sept 2026

Brief summary (registry, in English)

This study aims to assess the real-world patterns of disease modifying therapy (DMT) use before, during, and after pregnancy in women with multiple sclerosis (MS). The study will use a pooled closed claims database containing closed payer medical and pharmacy claims data for patients in the United States (US).

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
2607 (estimated)
First submitted
21 Sept 2026
Start date
6 Mar 2026
Primary completion date
30 Oct 2026
Lead sponsor
Novartis Pharmaceuticals
NCT number
NCT07844070

What you commit to

  • Study type: Observational
  • Planned participants: 2607
  • From 6 Mar 2026 to the primary completion date, 30 Oct 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Malignancy in pre-conception, pregnancy, or post-delivery periods.

Other

  • Pregnancies involving multiples, subject to data availability.

Who the study is looking for

  • ≥1 claim with a diagnosis or procedure code for live birth during the patient identification period (index date).
    • o Note: For patients with more than one pregnancy in the patient identification period, all eligible pregnancies will be included.
  • Female sex recorded on enrollment record overlapping with index date.
  • Aged between 18 and 49 years old at index date.
  • ≥2 claims with an MS diagnosis (International Classification of Diseases, Tenth Revision, Clinical Modification (ICD-10-CM) code G35) ≥30 days apart in the pre-conception or pregnancy periods.
  • Continuous healthcare plan enrollment from ≥6 months prior to the conception date to ≥6 months following the index date.

Age in the registry: 18 years to 49 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Novartis
Coordinator of this site? Confirm its status
East HanoverUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.