A Compassionate Access Protocol For Those Patients Who Have Completed A4001029

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NCT00801515

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Study Location
Pfizer Investigational Site
Montreal, Quebec, H3G 1A4, Canada
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Contact
1-800-718-1021
[email protected]
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Eligibility Criteria
condition
The disease, disorder, syndrome, illness, or injury that is being studied.
HIV
Sex
Females and Males
Age
Pediatric Trials: 0-17 Years
Adult Trials: 18+ Years
18 + years
Inclusion Criteria
The factors, or reasons, that allow a person to participate in a clinical study.
Show details

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

Exclusion Criteria
The factors, or reasons, that prevent a person from participating in a clinical study.
Show details


- None

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Advanced Information
Descriptive Information
Brief Title A Compassionate Access Protocol For Those Patients Who Have Completed A4001029
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.
Detailed Description Not Provided
Study Type Expanded Access
Intervention Drug: Maraviroc
150 mg twice per day
Other Name: Celsentri
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Expanded Access Status No longer available
Contacts Contact information is only displayed when the study is recruiting subjects
Listed Location Countries Canada
Removed Location Countries  
 
Administrative Information
NCT Number NCT00801515
Responsible Party Director, Clinical Trial Disclosure Group, Pfizer, Inc.
Study Sponsor ViiV Healthcare
Collaborators Pfizer
Investigators
Study Director:Pfizer CT.gov Call CenterPfizer
PRS Account ViiV Healthcare
Verification Date July 2011