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Characterization of Early Patients Initiating Ofatumumab for Treatment of Multiple Sclerosis.

Characterization of Early Patients Initiating Ofatumumab for Treatment of Multiple Sclerosis in the Real-World

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05576779
Enrollment
2101
Registered
2022-10-13
Start date
2020-12-03
Completion date
2021-12-31
Last updated
2022-11-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple Sclerosis

Keywords

Multiple sclerosis,, ofatumumab,, disease-modifying therapy,, COVID-19

Brief summary

This was a retrospective cohort study utilizing secondary data from IQVIA's open source pharmacy claims database (i.e., IQVIA LRx) selecting patients with prescription claims for ofatumumab or other DMTs of interest.

Detailed description

The date of first ofatumumab prescription claim or other DMT of interest was defined as the index date. No post-index requirements were imposed. Patients were linked to IQVIA's open source medical claims databases (Dx) to obtain patient clinical characteristics. The initial data were extracted in October 2020. The data and results were refreshed in April 2021 and July 2021 to allow for assessment of changes in characteristics at 6 and 9 months post-launch.

Interventions

All eligible patients with at least 1 claim for ofatumumab observed during the index period were included in the ofatumumab cohort

Sponsors

Novartis Pharmaceuticals
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* Patients with ≥ 1 prescription for ofatumumab in the LRx/Dx database were included. The date of the first observed prescription within the index window served as the index date. -. Patients with a diagnosis of COVID-19 or a COVID-19 vaccination any time during the study period. * Patients with linkage to the Dx database.

Exclusion criteria

\- No

Design outcomes

Primary

MeasureTime frameDescription
Proportion of patients initiating ofatumumab based on DMT use12-months prior to index date, where index date was defined as the date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts)The primary measure was pre-index treatment status of patients initiating ofatumumab, measured as proportion (n, %) of DMT-naïve and DMT-experienced patients among patients initiating ofatumumab based on DMT use in the 12-month pre-index period.

Secondary

MeasureTime frameDescription
GenderIndex date, defined as the date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts)Gender information was reported
Number of patients: Geographic regionIndex date, defined as the date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts)Northeast, Midwest, South, West, Unknown
Number of patients: State level (Geographic region)Index date, defined as the date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts)The geographical heat map of ofatumumab utilization at the state level was presented.
Number of patients: Insurance typeIndex date, defined as the date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts)Cash, Commercial, Medicare, Medicare Part D, Medicaid, Unknown
Number of patients: PayerIndex date, defined as the date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts)CVS, Aetna etc
Follow-up timeVariable Post-index period, where index date was defined as date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts) (01/08/2019 - 31/05/2021)Ofatumumab persistence was assessed over the variable follow-up time.
Number of patients: Pre-index Charlson comorbidity index (CCI)12-months prior to index date, where index date was defined as the date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts)Charlson Comorbidity Index predicts the ten-year mortality for a patient who may have a range of comorbid conditions. omorbidity was assessed using the Charlson Comorbidity Index (CCI), categorized as low (0-1) and high (≥2)
Number of patients: Pre-index comorbidities12-months prior to index date, where index date was defined as the date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts)Number of patients with list of comorbidities were reported
Number of patients with a relapse in inpatient settings12-months prior to index date, where index date was defined as the date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts)Number of patients with MS relapses were reported
Number of patients with a relapse in outpatient settings12-months prior to index date, where index date was defined as the date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts)Number of patients with MS relapses were reported
Number of relapses in all patients12-months prior to index date, where index date was defined as the date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts)Number of patients with MS relapses were reported
Number of relapses in patients with at least 1 relapse12-months prior to index date, where index date was defined as the date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts)Number of patients with MS relapses were reported
Claims-Based Disability Score12-months prior to index date, where index date was defined as the date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts)Pre-index MS-related symptoms and secondary conditions (n, %) based on a Claims-Based Disability Score (e.g., sensory problems, eye symptoms, pyramidal symptoms, bladder/bowel symptoms, fatigue/malaise, muscular weakness, durable medical equipment utilization.
Number of pre-index Brain and Spinal MRI scans12-months prior to index date, where index date was defined as the date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts)Categorized as: No MRI, 1, 2, 3+
Number of patients: Hepatitis B virus screening12-months prior to index date, where index date was defined as the date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts)Yes/No
Number of patients: Quantitative serum immunoglobulin screening12-months prior to index date, where index date was defined as the date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts)Yes/No
AgeIndex date, defined as the date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts)Age information was reported
Number of patients: Post-index flu shotVariable Post-index period, where index date was defined as Date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts) (01/08/2019 - 31/05/2021)Yes/No
Pre-index: Number of patients with COVID-19 diagnosis12-months prior to index date, where index date was defined as the date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts)Yes/No
Post-index: Number of patients with COVID-19 diagnosisVariable Post-index period, where index date was defined as Date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts) (01/08/2019 - 31/05/2021)Yes/No
Days between COVID-19 diagnosis and initiation of ofatumumabVariable Post-index period, where index date was defined as Date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts) (01/08/2019 - 31/05/2021)Days between COVID-19 diagnosis and initiation of ofatumumab were reported
Pre-index: Number of patients with COVID-19 vaccination12-months prior to index date, where index date was defined as the date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts)Yes/No
Post-index: Number of patients with COVID-19 vaccinationVariable Post-index period, where index date was defined as Date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts) (01/08/2019 - 31/05/2021)Yes/No
Days between COVID-19 vaccination and initiation of ofatumumabVariable Post-index period, where index date was defined as Date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts) (01/08/2019 - 31/05/2021)Days between COVID-19 vaccination and initiation of ofatumumab were reported.
Proportion of patients with steroid use or antihistamine as pre-medication with ofatumumab first doseVariable Post-index period, where index date was defined as Date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts) (01/08/2019 - 31/05/2021)E.g. diphenhydramine, dexamethasone and other steroids. pre-medication was defined as medication observed within two days of ofatumumab initiation.
Pre-index HCRU: Number of patients with an inpatient visit12-months prior to index date, where index date was defined as the date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts)Number of patients with an inpatient visits were reported to report the pre-index healthcare resource utilization
Pre-index HCRU: Number of patients with an ED visit12-months prior to index date, where index date was defined as the date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts)Number of patients with an ED visit were reported to report the pre-index healthcare resource utilization
Pre-index HCRU: Number of patients with an outpatient visit12-months prior to index date, where index date was defined as the date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts)Number of patients with an outpatient visit were reported to report the pre-index healthcare resource utilization
Pre-index HCRU: Number of patients with a pharmacy claim12-months prior to index date, where index date was defined as the date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts)Number of patients with a pharmacy claim were reported to report the pre-index healthcare resource utilization
Post-index HCRU: Number of patients with an inpatient visitVariable Post-index period, where index date was defined as Date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts) (01/08/2019 - 31/05/2021)Number of patients with an inpatient visits were reported to report the post-index healthcare resource utilization accrued while on ofatumumab
Post-index HCRU: Number of patients with an ED visitVariable Post-index period, where index date was defined as Date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts) (01/08/2019 - 31/05/2021)Number of patients with an ED visit were reported to report the post-index healthcare resource utilization accrued while on ofatumumab
Post-index HCRU: Number of patients with an outpatient visitVariable Post-index period, where index date was defined as Date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts) (01/08/2019 - 31/05/2021)Number of patients with an outpatient visit were reported to report the post-index healthcare resource utilization accrued while on ofatumumab
Post-index HCRU: Number of patients with a pharmacy claimVariable Post-index period, where index date was defined as Date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts) (01/08/2019 - 31/05/2021)Number of patients with a pharmacy claim were reported to report the post-index healthcare resource utilization accrued while on ofatumumab
Number of patients: Pre-index flu shot12-months prior to index date, where index date was defined as the date of first ofatumumab claim (or other DMT of interest for non-ofa cohorts)Yes/No

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026