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DOLOMITE NEAT ID Network Study: A Prospective, Multi-site Observational Study to Define the Safety and Effectiveness of Dolutegravir Use in HIV Positive Pregnant Women

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Observational
SUMMARY

The purpose of this study is to assess the safety and effectiveness of DTG use in HIV positive pregnant women. This is a 3-year multi-site prospective observational study. Approximately, 250 HIV positive pregnant women from potential European AIDS Treatment Network (NEAT ID) sites across Europe will be enrolled. The enrollment period will be over 2 years with a follow-up period of 1 year for outcomes. The data collected will be that obtained during routine standard of care assessments; and the subjects will not undergo any interventional study procedures.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• HIV positive pregnant women aged 18 years and over on DTG

• With no maternal or birth outcomes yet

• Subjects are able and willing to provide written informed consent and comply with any safety reporting requirements.

Locations
Other Locations
Spain
GSK Investigational Site
RECRUITING
Barcelona
Contact Information
Primary
US GSK Clinical Trials Call Center
GSKClinicalSupportHD@gsk.com
877-379-3718
Backup
EU GSK Clinical Trials Call Center
GSKClinicalSupportHD@gsk.com
+44 (0) 20 89904466
Time Frame
Start Date: 2019-11-18
Estimated Completion Date: 2024-10-30
Participants
Target number of participants: 250
Treatments
HIV positive pregnant women
Data from approximately 250 HIV positive pregnant women with exposure to DTG from potential investigational sites across Europe will be included.
Related Therapeutic Areas
Sponsors
Leads: ViiV Healthcare

This content was sourced from clinicaltrials.gov