Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
ViiV Healthcare
With
GlaxoSmithKline
Age
16–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Evidence of a personally signed and dated informed consent document indicating that the subject (or a legally acceptable representative) has been informed of all pertinent aspects of the study.
Subject has participated in a clinical trial that evaluated maraviroc and is continuing to derive clinical benefit from maraviroc treatment.
Subject agrees to the specified study procedures.
You may not be if
Subject who is an investigational site staff member or an employee of the Sponsor that is directly involved in the conduct of the trial.
Other severe, acute, or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation and, in the judgment of the investigator, would make the subject inappropriate for entry into this study.
Contra-indications to use of maraviroc as described in the Investigator Brochure.
Past documented dual/mixed or C-X-C chemokine receptor type 4 HIV tropism.
Clareo Health | An Expanded Access Protocol for Subjects Who Have Completed Clinical Studies Involving Maraviroc
