Pacritinib Effectiveness in Real-world Settings
Part of paid clinical trials in New Haven, Connecticut.
- Sponsor
- Swedish Orphan Biovitrum
- Study ID
- NCT07774455
- Status
- Recruiting
Conditions
- Myelofibrosis (MF)
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Not applicable- observational study — OTHERNot Applicable - Observational Study
Study Details
This study aims to evaluate real-world treatment patterns and effectiveness of pacritinib, including hematologic and clinical outcomes, and survival through a site-based retrospective chart review of medical records of patients with MF.
Key Dates
- First listed
- Aug 19, 2026
- Start date
- Aug 13, 2026
- Status verified
- Sep 2026
- Primary completion
- Jan 27, 2027
- Completion
- Jan 27, 2027
Study Design
- Enrollment
- 60 participants (estimated)
Primary Outcome Measure
≥50% spleen length reduction [ Time Frame: From the Index Date to Week 24 or best response in spleen reduction, assessed up to 49 months. ]
Central Contacts
- IQVIA Study Team617-621-1600
- Clinical Operations Lead
Locations (3)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Yale School of Medicine | New Haven | Connecticut | 06511 | Podoltsev |
| The Ohio State University | Columbus | Ohio | 43210 | Srisuwananukorn |
| Medical University of South Carolina | Charleston | South Carolina | 29425 | Coltoff |
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