Clinical Trials Directory

Trials / Terminated

TerminatedNCT01688011

Connect® Myeloid Disease Registry

Connect® Myeloid: The Myelofibrosis (MF), Myelodysplastic Syndromes (MDS) and Acute Myeloid Leukemia (AML) Disease Registry

Status
Terminated
Phase
Study type
Observational
Enrollment
2,013 (actual)
Sponsor
Celgene · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of the Connect® Myeloid disease registry is to provide unique insights into treatment decisions and treatment patterns as they relate to clinical outcomes of patients with myeloid diseases in routine clinical practice. This disease registry will also evaluate molecular and cellular markers that may provide further prognostic classification which may or may not be predictive of therapy and clinical outcomes.

Detailed description

This Disease Registry will collect data on patient characteristics, treatment patterns and clinical outcomes. The objective is to describe how patients with myeloid diseases are treated; and to build a knowledge base regarding the effectiveness and safety of first line and subsequent treatment regimens in both community and academic settings. Enrolled patients will receive treatment and evaluations for their disease according to the standard of care and routine clinical practice at each study site. All treatments that patients receive for their disease will be recorded, including initial treatment and any subsequent therapy. Data on treatment outcomes, including response rates as measured by the treating physician, evidence of progression, survival, and patient-reported outcomes will be collected quarterly on the electronic CRF.

Conditions

Interventions

TypeNameDescription
DRUGLuspaterceptPrescribed by treating physician as per product label.

Timeline

Start date
2013-12-12
Primary completion
2024-10-18
Completion
2024-10-18
First posted
2012-09-19
Last updated
2025-07-03

Locations

158 sites across 2 countries: United States, Puerto Rico

Regulatory

Source: ClinicalTrials.gov record NCT01688011. Inclusion in this directory is not an endorsement.