Trial record 20 of 33 for:    " May 05, 2010":" June 04, 2010"[FIRST-RECEIVED-DATE]AND HIV[CONDITION]

Novel Interventions in HIV-1 Infection (IMIRC1003)

This study has been terminated.
(Data from the 12 patients recruited has now been analysed, and it has been determined that it is sufficient to meet the study objectives.)
Sponsor:
Collaborator:
Medical Research Council
Information provided by (Responsible Party):
Imperial College London
ClinicalTrials.gov Identifier:
NCT01130376
First received: May 25, 2010
Last updated: September 2, 2013
Last verified: September 2012
  Purpose

For several years there has been interest in why some people with HIV-1 progress more slowly to disease and have longer survival without Highly Active Antiretroviral Therapy (HAART) than others. The investigators and others have identified a few HIV positive individuals who can control their viral load for many years without HAART, these rare individuals do not lose their HIV-1-specific cellular immune responses, which are very important for controlling viral load. This group is referred to as long-term non-progressors (LTNP). Unlike LTNP the majority of HIV-1 infected individuals are chronic progressors (CP) who do not make effective HIV-1-specific cellular immune responses, even when on HAART. We propose to use a novel DNA vaccine boosted with immune based therapy (cytokines and hormones) to try to regenerate the missing HIV-1-specific cellular immune responses to make chronically infected HIV-1+ persons more like LTNP.

By injecting this novel DNA vaccine and immune based therapy into the people who are already infected with HIV-1, the immune system may be stimulated to mount a greater immune response not only to the vaccines but also to real HIV-1 particles and HIV-1-infected cells.


Condition Intervention Phase
HIV-1 Infection
Biological: GTU-MultiHIV B clade vaccine1mg
Drug: Interleukin-2
Drug: GM-CSF
Drug: Growth Hormone
Phase 1

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: A Randomised, Open Labelled, Phase I, Safety, Toxicity, and Exploratory Immunogenicity Evaluation of Therapeutic Immunisation +/- IL-2, GM-CSF and Growth Hormone in HIV-1 Infected Subjects Receiving Highly Active Anti-retroviral Therapy

Resource links provided by NLM:


Further study details as provided by Imperial College London:

Primary Outcome Measures:
  • The primary outcome will be analysis of safety and toxicity data in relation to grade 3 or above laboratory or clinical serious adverse event (SAE) which can be attributed to the treatments given [ Time Frame: Weekly ] [ Designated as safety issue: Yes ]

Secondary Outcome Measures:
  • The secondary immunological outcomes will be percentage change from baseline to study time point in defined cellular immune responses. [ Time Frame: weekly ] [ Designated as safety issue: No ]

Enrollment: 12
Study Start Date: September 2009
Study Completion Date: October 2011
Primary Completion Date: October 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Vaccine and cytokines

Day 0: Patients receive GTU-MultiHIV B clade vaccine 1mg/ml administered as 10 intradermal injections of 100 µl/injection.

Day 7-11: One week following this, patients receive a 5 day course of Cytokines: Aldesleukin (IL-2) Novartis UK (BD; 8 hours apart) 5 million units administered by SC injection. Sargramostim (GM-CSF) - Leukine™, Berlex Seattle US 150ug SC once daily 4 hours from rhIL-2 injections.

Day 14-18: The following week, patients rhGH (Saizen™, Serono International, Geneva, Switzerland) 4mg/day self-administered SC.

Further vaccine boosters are given on day 42 and day 84. GTU-MultiHIV B clade vaccine 1mg/ml being administered as 10 intradermal injections of 100 µl/injection.

Biological: GTU-MultiHIV B clade vaccine1mg
Dose given is 1mg/ml administered as 10 intradermal injections of 100 µl/injection distributed as 5 intradermal injections /left and right arm
Drug: Interleukin-2
5 Million Units administered twice daily for 5 days by subcutaneous injection on days 7, 8, 9, 10, and 11 after first vaccination. .
Other Names:
  • Aldesleukin
  • Proleukin
Drug: GM-CSF
150 ug administered subcutaneously once daily 4 hours from IL-2 injections
Other Names:
  • Sargramostim
  • Leukine
Drug: Growth Hormone
4mg/day will be self administered by Subcutaneous injection for 5 days on days 14, 15, 16, 17 and 18 following first vaccination
Other Name: Serono International, Geneva, Switzerland
Active Comparator: Vaccine alone

Day 0: Patients are given GTU-MultiHIV B clade vaccine 1mg/ml administered as 10 intradermal injections of 100 µl/injections.

Day 42: GTU-MultiHIV B clade vaccine as day 0.

Day 84: GTU-MultiHIV B clade vaccine as day 0.

Biological: GTU-MultiHIV B clade vaccine1mg
Dose given is 1mg/ml administered as 10 intradermal injections of 100 µl/injection distributed as 5 intradermal injections /left and right arm
Active Comparator: Cytokines alone

Day 7-11: One week following this, patients receive a 5 day course of Cytokines: Aldesleukin (IL-2) Novartis UK (BD; 8 hours apart) 5 million units administered by SC injection. Sargramostim (GM-CSF) - Leukine™, Berlex Seattle US 150ug SC once daily 4 hours from rhIL-2 injections.

Day 14-18: The following week, patients rhGH (Saizen™, Serono International, Geneva, Switzerland) 4mg/day self-administered SC.

Drug: Interleukin-2
5 Million Units administered twice daily for 5 days by subcutaneous injection on days 7, 8, 9, 10, and 11 after first vaccination. .
Other Names:
  • Aldesleukin
  • Proleukin
Drug: GM-CSF
150 ug administered subcutaneously once daily 4 hours from IL-2 injections
Other Names:
  • Sargramostim
  • Leukine
Drug: Growth Hormone
4mg/day will be self administered by Subcutaneous injection for 5 days on days 14, 15, 16, 17 and 18 following first vaccination
Other Name: Serono International, Geneva, Switzerland

Detailed Description:

This will be a randomised, Phase I, open label comparative study running for 52 weeks (2 screen visits 2 weeks apart followed by 48 weeks of study). 50 patients will be screened in the initial phase of which 30 clade B infected individuals will be randomised into the study, which will consist of 3 arms:

Arm 1 will ascertain vaccine safety and toxicity in the presence of cytokine/hormone therapy.

Arm 2 will identify vaccine safety and toxicity.

Arm 3 will indicate safety and toxicity of cytokine/hormone therapy.

The target patients are chronically HIV-1 clade B infected persons who will have had a nadir CD4 T-cell count of >200 cells/ul blood before they started ART. The current CD4 T-cell count should be >400 cells/ul blood. Patients may have received ART for any length of time, but currently should be receiving NNRTI or boosted-PI based HAART, and have a viral load below the level of detection (50 copies/ml plasma). Patients will be bled on two occasions before commencing IBT regimens, in order to establish baselines, and then at regular intervals thereafter (weeks 0,1,2,4,6,8,12,16,24 and 48).

The treatment regimens are consistent with previous findings in animal models which suggest that administration of IL−2 during the antigen−specific T−cell contraction phase of an immune response (between 8 and 15 days post−vaccination) may preserve and lengthen clinically relevant responses. Furthermore studies in man have demonstrated that IL−2 administered before immunisation in ART−treated HIV−1−infected patients does not increase specific lymphoproliferation of T cells.

Recent preliminary studies in HIV−1−infected individuals using tetanus vaccines the investigators have shown that IL−2 administered after immunisation may be more effective at inducing sustained tetanus−specific responses than IL−2 administered before immunisation or together with immunisation. The dosages used in this study are based on those used in previous pilot studies of the administration of IL-2 + GM-CSF and rhGH and at these levels the drugs have been shown to have both positive effect on the immune response and demonstrated clinical benefit whilst being at a level which is safe and well tolerated in HIV-1 positive individuals. The dosage of the vaccine was based on a previous study where a dosage of this level has been shown to induce an immune response although this response was transient. In summary the investigators aim to increase the survival of vaccine responses through the administration of cytokines/hormones and boost memory responses with further rounds of immunisation.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Documented HIV-1 positive result.
  • Stable on HAART.
  • Two screening viral loads of <50 cps/ml on 2 consecutive occasions at least one month apart.
  • CD4 T cell count of >400 cells/ul.
  • Nadir CD4 T cell count of >200 cells/ul.
  • Over 18 years of age.
  • Willing and able to provide informed consent.
  • Female subjects must not be pregnant or lactating.
  • Subjects must be using adequate double barrier method of contraception as appropriate.

Exclusion Criteria:

  • Prior therapeutic vaccination.
  • Acute illness within 2 weeks of the start of the study.
  • Prior immunomodulatory therapy (e.g. IL-2, rhGH, GCSF, GM-CSF, HU)
  • Receiving immunosuppressive medication (e.g. Steroids)
  • Participation in other vaccine trials currently
  • Patients with diabetes mellitus type 2
  • Patients with cardiac abnormalities
  • Patients with pre-existing autoimmune disease
  • Patients with active neoplasia
  • Patients with evidence of any progression or recurrence of an underlying intra-cranial lesion
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01130376

Locations
United Kingdom
St. Stephen's AIDS Trust
London, United Kingdom, SW10 9NH
Sponsors and Collaborators
Imperial College London
Medical Research Council
Investigators
Principal Investigator: Nesrina Imami, MD/PhD Imperial College London
  More Information

Additional Information:
No publications provided

Responsible Party: Imperial College London
ClinicalTrials.gov Identifier: NCT01130376     History of Changes
Other Study ID Numbers: CRO930, G0501957, 2008-000575024
Study First Received: May 25, 2010
Last Updated: September 2, 2013
Health Authority: United Kingdom: Medicines and Healthcare Products Regulatory Agency
United Kingdom: Research Ethics Committee

Keywords provided by Imperial College London:
Immune based therapy
Therapeutic vaccination
cytokine therapy
HIV therapeutic vaccine

Additional relevant MeSH terms:
HIV Infections
Lentivirus Infections
Retroviridae Infections
RNA Virus Infections
Virus Diseases
Sexually Transmitted Diseases, Viral
Sexually Transmitted Diseases
Immunologic Deficiency Syndromes
Immune System Diseases
Hormones
Aldesleukin
Interleukin-2
Hormones, Hormone Substitutes, and Hormone Antagonists
Physiological Effects of Drugs
Pharmacologic Actions
Antineoplastic Agents
Therapeutic Uses
Analgesics, Non-Narcotic
Analgesics
Sensory System Agents
Peripheral Nervous System Agents
Central Nervous System Agents
Anti-HIV Agents
Anti-Retroviral Agents
Antiviral Agents
Anti-Infective Agents

ClinicalTrials.gov processed this record on July 09, 2014