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Nevirapine + 3TC Based Maintenance Therapy for HIV Infection (NVP+3TC)

Primary Purpose

HIV Infections

Status
Completed
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Nevirapine plus lamivudine
Sponsored by
Cantonal Hospital of St. Gallen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV Infections

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • HIV-pos, 18 years
  • Stable ART, Nevirapine based (plus 2 nukleotide-analogues), at least 6 months
  • Viral load suppression at least 24 months Prior to inclusion (<50cp/ml)

Exclusion Criteria:

  • chronic Hepatitis B necessitating tenofovir therapy

Sites / Locations

  • Kantonsspital St. Gallen

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

nevirapine plus lamivudine

Arm Description

patients from one Center switching from a Nevirapine based Regimen on Nevirapine + 3TC

Outcomes

Primary Outcome Measures

Treatment failure defined as HIV-RNA > 100 cp/ml
Patients reaching a viral load measurement >100cp /ml (confirmed) within the first 24 weeks of therapy with monthly HIV-RNA testing.

Secondary Outcome Measures

Full Information

First Posted
December 15, 2016
Last Updated
July 16, 2018
Sponsor
Cantonal Hospital of St. Gallen
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1. Study Identification

Unique Protocol Identification Number
NCT03223402
Brief Title
Nevirapine + 3TC Based Maintenance Therapy for HIV Infection
Acronym
NVP+3TC
Official Title
NEVIRAPINE Plus LAMIVUDINE (3TC) for HIV Maintenance Therapy - A Single Center Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
July 2018
Overall Recruitment Status
Completed
Study Start Date
December 23, 2016 (Actual)
Primary Completion Date
May 15, 2018 (Actual)
Study Completion Date
May 31, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cantonal Hospital of St. Gallen

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Type of study: Investigator initiated clinical study Study design: One arm, open label, pilot study (n=10) Research question Is treatment with Nevirapine + 3TC sufficient for HIV maintenance Risk Category B (no investigational drugs, non standard Tx) Therapies with 2 drugs are often done in HIV-maintenance. This is a systematical evaluation of such a two drug trial. Rescue therapy is well defined within the protocol. Centers (n) St. Gallen only Participants 10 HIV Patients already on nevirapine + 2 non-nuke RT-Inhibitors Study duration 24 weeks primary observation period after study termination, patients may opt to continue on the bi-therapy. Clinical follow up will then continue Sponsor/Investigator Pietro Vernazza, Kantonsspital St. Gallen Principal investigator Pietro Vernazza, MD. Kantonsspital St. Gallen Co-Investigators Patrick Schmid, MD, Matthias Hoffmann, MD Financial source None (Pilot Study) If study demonstrates good results, an SNF grant proposal will be submitted
Detailed Description
This is a pilot study to evaluate the efficacy of a two drug combination for Long term HIV maintenance therapy. The study is conducted in order to confirm the feasibility of the combination of Nevirapine and lamivudine (3TC) in patients with long term fully suppressive therapy. Patients (n=10) with a stable (>6 months) Nevirapine based triple therapy and a full viral load suppression for at least 2 years will continue their therapy for 6 months with Nevirapine+3TC. The primary endpoint is treatment failure defined as an HIV-RNA value >100 cp/ml, confirmed by a second measurement. Preliminary stopping rules are defined if results indicate futility. Futility is defined as a situation, where the investigators would stop their plan to conduct a multicenter comparative trial. Futility is reached, when the study documents more than 1 failure in the first 5 patients over 24 weeks of observation or more than 2 failures in all 10 patients. Only 10 patients will be followed in this single center pilot study. After an amendement (April 2017) the total number of 20 patients was increased to 20. Futility was defined as more than 2 failures in 20 patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Pilot study, one arm. We do not evaluate a specific drug. It is an Evaluation of a combination with just two instead of three drugs for the Treatment of HIV
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
nevirapine plus lamivudine
Arm Type
Experimental
Arm Description
patients from one Center switching from a Nevirapine based Regimen on Nevirapine + 3TC
Intervention Type
Other
Intervention Name(s)
Nevirapine plus lamivudine
Intervention Description
In this Pilot study, the efficacy of a bi-therapy consisting of NVP+3TC instead of NVP+2NRTI should be evaluated before a large multicenter study evaluating this combination is started.
Primary Outcome Measure Information:
Title
Treatment failure defined as HIV-RNA > 100 cp/ml
Description
Patients reaching a viral load measurement >100cp /ml (confirmed) within the first 24 weeks of therapy with monthly HIV-RNA testing.
Time Frame
24 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: HIV-pos, 18 years Stable ART, Nevirapine based (plus 2 nukleotide-analogues), at least 6 months Viral load suppression at least 24 months Prior to inclusion (<50cp/ml) Exclusion Criteria: chronic Hepatitis B necessitating tenofovir therapy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pietro L Vernazza, MD
Organizational Affiliation
KSSG
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kantonsspital St. Gallen
City
St. Gallen
State/Province
SG
ZIP/Postal Code
9007
Country
Switzerland

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
not planned

Learn more about this trial

Nevirapine + 3TC Based Maintenance Therapy for HIV Infection

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