Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
This was a retrospective descriptive analysis of health care claims data using the IQVIA open source medical and pharmacy claims databases.
Patients with a diagnosis of SCD between November 1, 2018 and April 30, 2021 were identified. Among these patients, those who initiated crizanlizumab between November 1, 2019 and January 31, 2021 (index period) were selected into the treatment cohort. The indexing timeframe allowed for a 1-year lookback period and a minimum of 3 months (3m cohort) of follow-up. A subset of the 3m cohort with 6-months of available (6m cohort) follow-up was performed. The index date was the date of the first crizanlizumab administration.
Study period: 01 November 2018 - 30 April 2021 Index period: 01 November 2019 - 31 January 2021 Index date: Date of the first claim for administration of crizanlizumab in the index period
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Overall cohort | All the patients who met the base inclusion criteria were included in the cohort. |
| |
| Three-month cohort (3m cohort) | Patients with stability and eligibility in IQVIA Patient Centric Medical Claims Database (Dx) and stability and eligibility in IQVIA Longitudinal Prescription Database (LRx) during the 3 months following the index date were included in the cohort. |
| |
| Six-month cohort (6m cohort) | A subset of patients from the 3m cohort with stability and eligibility in Dx and stability and eligibility in LRx during the 6 months following the index date were included in this cohort. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Crizanlizumab | Other | Patients who initiated crizanlizumab between November 1, 2019 and January 31, 2021 (index period) were selected into the treatment cohort. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Age | Age information was reported. | Baseline |
| Number of patients: Gender | Gender information was reported. | Baseline |
| Number of patients: Geographic region | The following categories were included: Northeast, Midwest, South, West | Baseline |
| Number of patients: Insurance type | When multiple payer types were observed, the following hierarchy was used: Medicare, Commercial, Medicaid, Cash, Unspecifed. When commercially-managed Medicaid was observed, the Medicaid designation was assigned. | Baseline |
| Number of patients by Charlson Comorbidity Index (CCI) score category | Severity of comorbidity was categorized into three grades: mild, with CCI scores of 1-2; moderate, with CCI scores of 3-4; and severe, with CCI scores ≥5. | Baseline |
| Number of patients by comorbidity | Number of patients by IQVIA's standard comorbidity list were reported. | Baseline |
| Number of patients with history of additional SCD-related comorbidities associated with organ damage | Number of patients with history of additional SCD-related comorbidities associated with organ damage were reported. | Baseline |
| Measure | Description | Time Frame |
|---|---|---|
| Proportion of patients with claims for hydroxyurea while on crizanlizumab therapy | Concomitant SCD treatments after initiating crizanlizumab | Throughout the follow-up period, approximately 1.5 years |
| Number of hydroxyurea claims |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
The study included patients with SCD who initiated crizanlizumab in a real-world setting
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Novartis Pharmaceuticals | Novartis Pharmaceuticals | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Novartis Investigative Site | East Hanover | New Jersey | 07936-1080 | United States |
Not provided
| Label | URL |
|---|---|
| Results for CSEG101AUS17 from the Novartis Clinical Trials Website | View source |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D000755 | Anemia, Sickle Cell |
| ID | Term |
|---|---|
| D000745 | Anemia, Hemolytic, Congenital |
| D000743 | Anemia, Hemolytic |
| D000740 | Anemia |
| D006402 | Hematologic Diseases |
Not provided
Not provided
| ID | Term |
|---|---|
| C000614139 | crizanlizumab |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Number of patients : History of hydroxyurea use |
Pre-index treatment history for sickle cell disease was reported. |
| Baseline |
| Number of patients : History of L-glutamine use | Pre-index treatment history for sickle cell disease was reported. | Baseline |
| Number of patients : History of Voxelotor use | Pre-index treatment history for sickle cell disease was reported. | Baseline |
| Number of patients : SCD genotype | Number of patients with sickle cell disease genotype were reported. | Baseline |
Concomitant SCD treatments after initiating crizanlizumab
| Throughout the follow-up period, approximately 1.5 years |
| Proportion of patients with claims for L-glutamine while on crizanlizumab therapy | Concomitant SCD treatments after initiating crizanlizumab | Throughout the follow-up period, approximately 1.5 years |
| Number of L-glutamine claims | Concomitant SCD treatments after initiating crizanlizumab | Throughout the follow-up period, approximately 1.5 years |
| Proportion of patients with claims for voxelotor while on crizanlizumab therapy | Concomitant SCD treatments after initiating crizanlizumab | Throughout the follow-up period, approximately 1.5 years |
| Number of voxelotor claims | Concomitant SCD treatments after initiating crizanlizumab | Throughout the follow-up period, approximately 1.5 years |
| D006425 |
| Hemic and Lymphatic Diseases |
| D006453 | Hemoglobinopathies |
| D030342 | Genetic Diseases, Inborn |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |