BREATHER (PENTA 16) Short-Cycle Therapy (SCT) (5 Days on/2 Days Off) in Young People With Chronic HIV-infection
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Purpose
The overall aim of the BREATHER trial is to evaluate the role of Short-Cycle Therapy (SCT) in the management of HIV-infected young people who have responded well to antiretroviral therapy (ART) and to determine whether young people with chronic HIV infection undergoing Short-Cycle Therapy of five days on ART and two days off maintain the same level of viral load suppression as those on continuous therapy, over 48 weeks.
To assess the advantages and disadvantages of the strategy, the incidence of toxicities, immunological control, resistance mutations, acceptability, quality of life and adherence to the randomised strategy will also be compared.
Importantly, because of insufficient data on short-term viral load rebound after stopping ART in this population, the trial will incorporate an initial pilot phase in selected centres, to assess the safety of the SCT strategy by evaluating detailed HIV-1 RNA profiles of participants on the SCT strategy.
| Condition | Intervention | Phase |
|---|---|---|
|
HIV |
Drug: efavirenz |
Phase 2 Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | BREATHER (PENTA 16) Short-Cycle Therapy (SCT) (5 Days on/2 Days Off) in Young People With Chronic HIV-infection |
- HIV-1 RNA ≥50 copies/ml (confirmed on a separate sample within 1 week) at any of week 4, 12, 24, 36 or 48. [ Time Frame: 48 weeks ] [ Designated as safety issue: Yes ]This outcome measure only considers HIV-1 RNA measurements at these time points due to the difference in viral load monitoring in the pilot phase and the main trial. However if a young person enrolled in the pilot phase has HIV-1 RNA ≥50 copies/ml at weeks 1, 2 or 3 (reproducible on the same sample) or at week 8 (confirmed on the same sample within 1 week), they will be considered as reaching the primary outcome at week 4 and 12 respectively
- HIV-1 RNA <50 c/ml at 24 and 48 weeks [ Time Frame: 24 and 48 weeks ] [ Designated as safety issue: No ]
- Number of HIV mutations present at week 4, 12, 24, 36 or 48 conferring resistance to drugs taken at randomisation or during the tria [ Time Frame: Weeks 4, 12, 24, 36, 48 ] [ Designated as safety issue: No ]
- Change in CD4 (absolute and percentage) from randomisation to 24 and 48 weeks [ Time Frame: 24 and 48 weeks ] [ Designated as safety issue: No ]
- Change in ART (defined as any change from the ART regimen at randomisation) [ Time Frame: 48 weeks ] [ Designated as safety issue: No ]
- Grade 3 or 4 clinical and laboratory adverse events [ Time Frame: 48 weeks ] [ Designated as safety issue: Yes ]
- ART treatment modifying adverse events (all grades) [ Time Frame: 48 weeks ] [ Designated as safety issue: No ]
- New CDC stage B or C diagnosis or death [ Time Frame: 48 weeks ] [ Designated as safety issue: No ]
- Changes in fasting glucose, cholesterol, triglycerides, LDL, HDL and VLDL levels through 48 weeks [ Time Frame: 48 weeks ] [ Designated as safety issue: No ]
- Adherence, acceptability, and quality of life over 48 weeks as assessed by patient completed questionnaires [ Time Frame: 48 weeks ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 160 |
| Study Start Date: | April 2011 |
| Estimated Study Completion Date: | August 2014 |
| Estimated Primary Completion Date: | November 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: Continuous Therapy
Continue with current antiretroviral therapy regime as per standard care
|
Drug: efavirenz
May be taken as 600mg tablet, 200mg tablet or as part of a combination pill
Other Name: Trade name: Sustiva
|
|
Experimental: Short Cycle Therapy
Take current antiretroviral therapy 5 days a week (2 days off) as instructed by clinician
|
Drug: efavirenz
May be taken as 600mg tablet, 200mg tablet or as part of a combination pill
Other Name: Trade name: Sustiva
|
Eligibility| Ages Eligible for Study: | 8 Years to 24 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- HIV-1 infected young people aged 8 to 24 years inclusive (Young people recruited between the ages of 16-21 must either be in regular physical contact with their clinician or be able to transfer to an adult physician at the same site for follow-up or to an affiliated adult site).
- Parents/carers and/or young people, where applicable, willing to provide informed consent.
- On a stable first-line ART treatment containing at least 2 NRTIs/NtRTIs and EFV for at least 12 months and willing to continue the regimen throughout the study period. Young people on regimens containing nevirapine (NVP) or a boosted protease inhibitor with undetectable viral load for over one year who wish to enrol should switch to EFV. Once they are stable on the EFV containing regimen for more than 12 weeks they may be enrolled (must have 2 subsequent HIV-1 RNA measurements <50 c/ml over a minimum period of 12 weeks). Previous dual therapy and/or substitution of NRTIs is allowed providing any changes were not for disease progression, immunological or virological failure (where virological failure is defined as two successive HIV-1 RNA results>1000 c/ml) subsequent to virological control having been achieved on ART.
- Viral suppression (HIV-1 RNA <50 c/ml) for at least the prior 12 months (at least the last 3 measurements, including screening): young people who have experienced a single viral load >50 but <1000 copies/ml (preceded and followed by VL<50 c/ml) in the last 12 months can be enrolled.
- CD4 cell count ≥350 106/L at screening visit.
- Centre must routinely use an assay which detects HIV RNA-1 viral load ≥50 c/ml.
Exclusion Criteria:
- Pregnancy or risk of pregnancy in females of child bearing potential.
- Acute illness (young people may be enrolled after illness).
- Receiving concomitant therapy for an acute illness (young people may be enrolled after finishing therapy).
- A creatinine, AST or ALT of grade 3 or above at screening.
- On a regimen including nevirapine or a boosted PI (young people may switch to an EFV based regimen).
- Previous ART monotherapy (except for the prevention of mother-to-child transmission)
Contacts and Locations| Contact: Diana M Gibb, MD | 2076704714 | dmg@ctu.mrc.ac.uk |
| United States, Tennessee | |
| St Jude Children's Research Hospital | Recruiting |
| Memphis, Tennessee, United States | |
| Contact: Patricia Flynn | |
| Brazil | |
| Emilio Ribas | Not yet recruiting |
| Sau Paulo, Brazil | |
| Contact: Marinella Della Negra | |
| France | |
| INSERM | Recruiting |
| Villejuif, France | |
| Contact: Alexandra Compagnucci | |
| Ireland | |
| Our Lady's Children's Hospital | Recruiting |
| Dublin, Ireland | |
| Contact: Karina Butler | |
| Thailand | |
| Program for HIV Prevention and Treatment (PHPT)/IRD 174 | Recruiting |
| Changklan, Muang, Chiang Mai, Thailand, 50100 | |
| Contact: Tim Cressey | |
| Sub-Investigator: Tim Cressey, MD | |
| HIV-NAT Thai Red Cross AIDS Research Centre | Recruiting |
| Bangkok, Thailand | |
| Contact: Jintanat Ananworanich | |
| Uganda | |
| Joint Clinical Research Centre | Recruiting |
| Kampala, Uganda | |
| Contact: Victor Musiime | |
| Ukraine | |
| Kiev City AIDS Center | Not yet recruiting |
| Kiev, Vidpochynku 11, Ukraine, 03115 | |
| Contact: Alla Volokha volokha@gmail.com | |
| Principal Investigator: Alla Volokha | |
| United Kingdom | |
| Birmingham Heartlands Hospital | Recruiting |
| Birmingham, United Kingdom | |
| Contact: Steven Welch | |
| University Hospital Bristol | Recruiting |
| Bristol, United Kingdom | |
| Contact: Jolanta Bernatoniene | |
| Leeds General Infirmary | Recruiting |
| Leeds, United Kingdom | |
| Contact: Philip Chetcuti | |
| Leicester Royal Infirmary | Recruiting |
| Leicester, United Kingdom | |
| Contact: Srinivas Bandi | |
| Great Ormond Street Hospital | Recruiting |
| London, United Kingdom | |
| Contact: Nigel Klein | |
| Evelina Children's Hospital | Recruiting |
| London, United Kingdom | |
| Contact: Esse Menson | |
| St George's Hospital | Recruiting |
| London, United Kingdom | |
| Contact: Katja Doerholt | |
| Mortimer Market Centre | Recruiting |
| London, United Kingdom | |
| Contact: Richard Gilson | |
| Nottingham University Hospital | Recruiting |
| Nottingham, United Kingdom | |
| Contact: Lucy Cliffe | |
| John Radcliffe Hospital | Not yet recruiting |
| Oxford, United Kingdom | |
| Contact: Brian Angus | |
| Principal Investigator: | Karina M Butler, MRCPI | Medical Research Council |
More Information
Additional Information:
No publications provided
| Responsible Party: | PENTA Foundation |
| ClinicalTrials.gov Identifier: | NCT01641016 History of Changes |
| Other Study ID Numbers: | BREATHER (PENTA 16), 2009-012947-40 |
| Study First Received: | July 12, 2012 |
| Last Updated: | January 15, 2013 |
| Health Authority: | United Kingdom: Medicines and Healthcare Regulatory Agency (MHRA) |
Keywords provided by PENTA Foundation:
|
short cycle therapy young people HIV |
Additional relevant MeSH terms:
|
HIV Infections Acquired Immunodeficiency Syndrome Lentivirus Infections Retroviridae Infections RNA Virus Infections Virus Diseases Sexually Transmitted Diseases, Viral Sexually Transmitted Diseases Immunologic Deficiency Syndromes Immune System Diseases Slow Virus Diseases |
Efavirenz Reverse Transcriptase Inhibitors Nucleic Acid Synthesis Inhibitors Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action Pharmacologic Actions Anti-Retroviral Agents Antiviral Agents Anti-Infective Agents Therapeutic Uses Anti-HIV Agents |
ClinicalTrials.gov processed this record on June 18, 2013