EUCTR2004-000948-25-ES
Active, not recruiting
Phase 1
Determinación de niveles plasmáticos e intracelulares de los inhibidores de la transcriptasa inversa análogos a nucleósidos (NRTI) y del análogo a nucleótido tenofovir disoproxil fumarato (TDF) en pacientes tratados con abacavir y/o lamivudina administrados con o sin TDF
Fundació de Lluita Contra la Sida0 sites27 target enrollmentSeptember 27, 2004
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Fundació de Lluita Contra la Sida
- Enrollment
- 27
- Status
- Active, not recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •HIV\-infected patients \>18 years old
- •Indetectable viral load
- •HAART receiving treatment during previous three months including lamivudine and/or ABC and TDF, with ritonavir/lopinavir or nevirapine
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1\.2 Adults (18\-64 years) yes
- •F.1\.2\.1 Number of subjects for this age range
- •F.1\.3 Elderly (\>\=65 years) yes
- •F.1\.3\.1 Number of subjects for this age range
Exclusion Criteria
- •Interruption of the theraphy during the study
- •Concomitant treatment with other medicinal products that should interaction with antirretroviral treatment
- •Concomitant treatment with other antirretroviral drugs during the study
Outcomes
Primary Outcomes
Not specified
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