Study identification

EU PAS number

EUPAS1000000053

Study ID

1000000053

Official title and acronym

CROSSROADS-2: Clinical Characteristics, Treatment Patterns, and Treatment Outcomes Among Users of Tezspire: An Electronic Medical Record (EMR) study (20220066)

DARWIN EU® study

No

Study countries

United States

Study description

Retrospective cohort study to describe the characteristics of patients treated with Tezspire (tezepelumab-ekko) in the real-world setting.
Additionally, this study will describe treatment patterns and asthma related clinical outcomes of patients initiating Tezspire.
Tezspire patients will be identified in the TriNetX Dataworks-USA network (a de-identified, longitudinal Electronic Medical Record (EMR)-derived dataset that includes outpatient and inpatient EMRs from 60 healthcare organizations (HCOs) across the US).

Study status

Ongoing
Research institutions and networks

Institutions

Amgen
United States
First published:
21/02/2024
Institution

Contact details

Global Development Leader Amgen Inc.

Primary lead investigator
Study timelines

Date when funding contract was signed

Planned:
Actual:

Study start date

Planned:
Actual:

Data analysis start date

Planned:

Date of final study report

Planned:
Sources of funding
Pharmaceutical company and other private sector 

More details on funding

Amgen 100%
Regulatory

Was the study required by a regulatory body?

No

Is the study required by a Risk Management Plan (RMP)?

Not applicable