Study of the Effectiveness and Safety of Darunavir/Cobicistat (DRV/c) Containing Regimens in Routine Clinical Practice

NCT03042390 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 762

Last updated 2020-02-05

No results posted yet for this study

Summary

This is a retrospective observational study of patients who have taken a regimen containing DRV / c at least 24 weeks prior to study initiation

Conditions

  • HIV Infections

Sponsors & Collaborators

  • Janssen-Cilag, S.A.

    collaborator INDUSTRY
  • Fundacion SEIMC-GESIDA

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-12-23
Primary Completion
2017-05-09
Completion
2017-05-09

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03042390 on ClinicalTrials.gov