Clinical Trials Directory

Trials / Terminated

TerminatedNCT02486510

Effect of Cytoreductive Chemotherapy and a CCR5 Coreceptor Antagonist on HIV-1 Eradication

Status
Terminated
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
7 (actual)
Sponsor
Fundacion para la Investigacion Biomedica del Hospital Universitario Ramon y Cajal · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

Effect on HIV-1 cell reservoirs of the concomitant administration of intensive chemotherapy and the pharmacological blockade of CCR5 coreceptors: a pilot, open, randomized, and controlled clinical trial.

Conditions

Interventions

TypeNameDescription
DRUGMaravirocPatients randomized to experimental control will start Maraviroc treatment before, during and after chemotherapy until lymphocytes level recovery. Maraviroc Dose: 300 mg/12 hours For patients receiving an HIV-protease inhibitor (except tipranavir or Fosamprenavir), the dose will be reduced to 150 mg/12hours For patients receiving Efavirenz dose the dose will be 600 mg/12hours

Timeline

Start date
2012-07-01
Primary completion
2015-12-01
Completion
2015-12-01
First posted
2015-07-01
Last updated
2015-12-18

Locations

2 sites across 1 country: Spain

Source: ClinicalTrials.gov record NCT02486510. Inclusion in this directory is not an endorsement.

Effect of Cytoreductive Chemotherapy and a CCR5 Coreceptor Antagonist on HIV-1 Eradication (NCT02486510) · Clinical Trials Directory