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A Compassionate Access Protocol For Those Patients Who Have Completed A4001029

A Compassionate Access Protocol For Those Patients Who Have Completed A4001029

Status
NO_LONGER_AVAILABLE
Phases
Unknown
Study type
Expanded Access
Source
ClinicalTrials.gov
Registry ID
NCT00801515
Enrollment
Unknown
Registered
2008-12-03
Start date
2009-08-31
Completion date
2011-07-31
Last updated
2011-07-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV

Keywords

Compassionate, HIV, CCR5

Brief summary

This is a compassionate study to provide continued access to maraviroc for only those subjects completing study A4001029 who are showing clinical benefit. Assessments of safety and tolerability of maraviroc when added to OBT will be continued.

Interventions

DRUGMaraviroc

150 mg twice per day

Sponsors

Pfizer
CollaboratorINDUSTRY
ViiV Healthcare
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients having completed study A4001029 in Canada and still deriving clinical benefit.

Exclusion criteria

* None

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026