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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT00062660
Registration number
NCT00062660
Ethics application status
Date submitted
10/06/2003
Date registered
12/06/2003
Date last updated
30/11/2016
Titles & IDs
Public title
Tipranavir in Patients With Progressive, Systemic HIV-1 Disease Who Have Failed or Are Intolerant to Currently Approved Treatments for HIV Infection
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Scientific title
An Open Label Safety Study to Evaluate the Safety of Tipranavir Plus Ritonavir When Used in Combination With Other Agents for the Treatment of Patients With HIV Infection Who Have Failed and/or Are Intolerant to Combination Antiretroviral Therapy and Have Limited Treatment Options
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Secondary ID [1]
0
0
1182.58
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
HIV Infections
0
0
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Condition category
Condition code
Infection
0
0
0
0
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Studies of infection and infectious agents
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Infection
0
0
0
0
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Other infectious diseases
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Infection
0
0
0
0
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Sexually transmitted infections
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Infection
0
0
0
0
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Acquired immune deficiency syndrome (AIDS / HIV)
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Intervention/exposure
Study type
Expanded Access
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Description of intervention(s) / exposure
Treatment: Drugs - Tipranavir
Treatment: Drugs: Tipranavir
Tipranavir 250 mg soft elastic capsules
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Intervention code [1]
0
0
Treatment: Drugs
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Comparator / control treatment
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Control group
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Outcomes
Eligibility
Key inclusion criteria
Inclusion criteria:
Patients aho have a positive serology HIV antibody test confirmed by Western blot, p24 antigen assay, HIV-1 RNA or HIV culture and are highly pre-treated and virus resistant to multiple protease inhibitors.
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Minimum age
2
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
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Study design
Purpose of the study
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Allocation to intervention
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
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Other design features
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Phase
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
APPROVED_FOR_MARKETING
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
1/05/2003
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
1/04/2014
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Sample size
Target
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
NSW,QLD,SA,VIC,WA
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Recruitment hospital [1]
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1182.58.61005 Royal Prince Alfred Hospital - Camperdown
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Recruitment hospital [2]
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1182.58.61008 St Vincents Hospital - Darlinghurst
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1182.58.61011 St Vincents Hospital - Darlinghurst
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1182.58.61014 St Vincents Hospital - Darlinghurst
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1182.58.61007 407 Doctors Pty Ltd - Darlinghusrst
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1182.58.61019 407 Bouke Street - Darlinghusrst
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1182.58.61022 Sexual Health Clinic - Kingswood
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Recruitment hospital [8]
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1182.58.61012 Bigge Park Centre - Liverpool
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Recruitment hospital [9]
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1182.58.61003 The Prince of Wales Hospital - Randwick
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1182.58.61002 Royal North Shore Hospital - St Leonards
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1182.58.61006 Albion Street Clinic - Surry Hills
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1182.58.61025 Immunology Department - Westmead
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Recruitment hospital [13]
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1182.58.61010 Biala Building - Brisbane
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1182.58.61009 Level 6 - Herston
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1182.58.61024 - Nambour
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1182.58.61016 Princess Alexandra Hospital - Woolloongabba
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1182.58.61020 - Adelaide
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1182.58.61015 Flinders Medical Centre - Bedford Park
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1182.58.61001 88 Rathdowne Street Carlton - Carlton
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1182.58.61018 Melbourne Sexual Health Clinic - Carlton
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1182.58.61017 Department of Infectious Diseases - Clayton
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1182.58.61013 Melbourne Sexual Health Clinic - Melbourne
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1182.58.61023 - Melbourne
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1182.58.61021 - South Yarra
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1182.58.61004 Royal Perth Hospital - Perth
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Recruitment postcode(s) [1]
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- Camperdown
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- Darlinghurst
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- Darlinghusrst
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- Kingswood
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- Brisbane
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- Herston
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- Nambour
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- Perth
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Funding & Sponsors
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Name
Boehringer Ingelheim
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Ethics approval
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Summary
Brief summary
To provide early access to tipranavir and evaluate the safety and tolerance of tipranavir combined with low dose of ritonavir in patients with progressive, HIV-1 disease who have failed or are intolerant to currently approved treatments for HIV infection, who are unable to participate in another tipranavir controlled clinical trial and have an urgent need for anti-HIV treatment.
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Trial website
https://clinicaltrials.gov/study/NCT00062660
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Contacts
Principal investigator
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Boehringer Ingelheim
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Boehringer Ingelheim
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Contact person for scientific queries
No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT00062660
Download to PDF