Clinical trial

United States Post-Marketing Observational Cardiovascular Safety Study in Patients Taking Naloxegol

Name
D3820R00008
Description
The overall research goal for this study is to provide additional data to characterize the safety of naloxegol in patients aged 18 years and older who do not have a diagnosis of cancer and who are treated with opioids chronically
Trial arms
Trial start
2016-06-24
Estimated PCD
2023-12-31
Trial end
2023-12-31
Status
Active (not recruiting)
Treatment
naloxegol
non-interventional study where naloxegol is prescribed during normal clinical practice
Arms:
naloxegol
non-PAMORA
non-interventional study where patients are exposed to non-peripherally acting mu-opioid antagonists during the normal course of clinical practice
Arms:
non-PAMORA
Size
8800
Primary endpoint
major adverse cardiovascular events
can occur anytime through study completion, given no fixed follow-up timepoints, which can range from 1 day to 8 years
Eligibility criteria
Inclusion Criteria: 1. Patient receives a new dispensing of naloxegol, lubiprostone/linaclotide, or an oral NNPAMORA. A new dispensing is one that occurs with no dispensing for the same drug having occurred in the preceding 182 days. A patient only qualifies once under this criterion for any drug. 2. Patients 18 years of age or older at the index date 3. Continuous availability of data for at least 183 days immediately before and including the index date 4. 90 days of opioid dispensed in the 183 days before and including the index date of which at least 30 days of opioid dispensed at at least 30 MEQ/day in the 60 days before and including index date 5. Current users of a dispensed opioid, meaning that the interval between index study drug dispensing and at least 1 prior opioid dispensing is less than the days supply associated with the opioid dispensing Exclusion Criteria: 1. Any medical care associated with a diagnosis of cancer in the 183 days before and including the index date; a diagnosis of cancer for this purpose is any diagnostic code of International Classification of Diseases, 9th revision (ICD-9) in the range 140-208 "Malignant neoplasms ..." or of the 10th revision (ICD-10) in the range C00-C96, "Malignant neoplasms" 2. Dispensing of methylnaltrexone for subcutaneous injection in the 183 days before and including the index date 3. Indication in the electronic records of the occurrence of MACE in the 183 days before and including the index date; see Section 9.3.2 "MACE" for screening criteria
Protocol
{'studyType': 'OBSERVATIONAL', 'patientRegistry': False, 'designInfo': {'observationalModel': 'COHORT', 'timePerspective': 'RETROSPECTIVE'}, 'enrollmentInfo': {'count': 8800, 'type': 'ESTIMATED'}}
Updated at
2023-05-15

1 organization

2 products

1 indication

Organization
Valinor Pharma
Product
naloxegol
Product
non-PAMORA