Effect of Cenicriviroc on HIV Neurocognitive Impairment

University of Hawaii

Status and phase

Completed

Phase 2

Conditions

Human Immunodeficiency Virus

HIV-1-Associated Cognitive Motor Complex

AIDS Dementia Complex

Treatments

Drug: cenicriviroc

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT02128828

H020

Details and patient eligibility

About

The study hypothesis is that cenicriviroc will improve cognition in HIV infected individuals with cognitive impairment. The investigators will study the effect of cenicriviroc on cognition in 24 subjects over a 24 week period.

Full description

HIV-associated neurocognitive disease (HAND), particularly in its milder form, is estimated to occur in greater than 30% of HIV infected individuals in the era of potent antiretroviral therapy. As even mild disease leads to functional consequences with decreased ability to live independently, HAND is of substantial public health concern. HIV-induced immune activation/inflammation of monocytes (MO) may be primarily responsible for the development of HAND.

Cenicriviroc is a combined CCR5 and CCR2 chemokine co-receptor antagonist. The investigators hypothesize that dual CCR5 and CCR2 blockade with the use of CVC will lead to measurable reductions in MO activation and lead to cognitive improvement by decreasing HIV infection of MO and by interrupting the trafficking of such MO into the central nervous system.

The investigators propose a single arm, 24-week trial of CVC in 24 subjects with HIV-1 infection suppressed on ART (plasma HIV RNA < 50 copies/ml) for 1 year or more with mild to moderate cognitive impairment.

Enrollment

20 patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

4.2.1.1 Documentation of HIV-1 infection by an FDA approved test at any time prior to study entry
On ARV medication uninterrupted for > 1 year leading up to the screening period
Screening plasma HIV RNA < 50 copies/ml within 3 months of entry
Willingness for males and females of childbearing potential to utilize 2 effective contraception methods (2 separate forms, one of which must be an effective barrier method), be non-heterosexually active or have a an exclusive vasectomized partner from screening throughout the duration of the study treatment and for 30 days following the last dose of study drugs.
Age 18 to 70 years
Ability and willingness to provide written informed consent
Mild to moderate cognitive impairment with global neuropsychological (NP) test (NPZglobal) score of < -0.5 or a neurocognitive abnormality (<-0.5) in at least one cognitive domain known to be typically affected by HIV OR unimpaired
On antiretroviral (ARV) therapy consisting of nucleoside reverse transcriptase inhibitors, atazanavir with/or without ritonavir, darunavir plus ritonavir, dolutegravir, raltegravir or efavirenz.

Exclusion criteria

Receiving or used a CCR5 antagonist within 6 months of study entry
Plasma HIV RNA > 100 copies/ml within 6 mo. of screening
HIV-2
Chronic hepatitis B (positive hepatitis B surface antigen)
Chronic hepatitis C (positive hepatitis C antibody), except with proof of viral clearance and normal liver function tests
Active or chronic liver disease
Active or inadequately treated tuberculosis infection, or inadequate treatment for a positive purified protein derivative test. Adequate treatment meets current recommendations of the Center for Disease Control, NIH and the HIV Medicine Association of the Infectious Diseases Society of America (IDSA) guidelines or other Center for Disease Control recommendations if patient was treated before the current recommendations or before coinfection with HIV.
Prior/current diagnosis with other intracellular pathogens (Listeria monocytogenes, Toxoplasma gondii, and Cryptococcus neoformans).
Uncontrolled seizures
Current or past malignancies excluding basal cell cancer and Kaposi's sarcoma (skin).
Immunomodulator, HIV vaccine, any other vaccine, or investigational therapy within 30 days of entry.
Requirement for acute therapy for AIDS-defining or other serious medical illnesses within 14 days of entry.
Other chronic illnesses including hematologic, pulmonary, autoimmune diseases and endocrinopathies, except for stable controlled diabetes or cardiovascular disease in the view of the investigator and stable testosterone or thyroid therapy.
Known hypersensitivity to CVC or its excipients
Anticipated need for prescription medication not allowed in the study. Unwilling to stop eating grapefruit or using St. John's wort).
Chronic use of over the counter medications unless approved by Study Investigator
Hemoglobin < 8.5; Absolute neutrophil count < 1000; Platelet count < 100,000; serum glutamate oxaloacetate and pyruvate transaminase > 2.5x upper limit of normal ; Lipase > 2.0 x upper limit of normal
Estimated creatinine clearance < 30 mL/min(Cockcroft and Gault 1979)
Bradycardia, sinus rhythm <50 beats/min (bpm).
Presence of any condition that would interfere with the absorption, distribution, metabolism, or excretion of the drug
Current active illicit substance or alcohol use or abuse which, in the judgment of the Investigator, will interfere with the patient's ability to comply with protocol requirements
Pregnancy or breast-feeding
History of moderate (Child-Pugh class B) or severe (Child-Pugh C) hepatic impairment
Patients, who, in the opinion of the Investigator, are unable to comply with the dosing schedule and protocol evaluation or for whom the study may not be advisable
For MRI substudy [impaired]: Any factor that precludes MRI scan including presence of metal or exposure to metal work (e.g. metal grinder/worker) and claustrophobia
For MRI substudy [impaired]: Any central nervous system pathology which, in the judgment of the investigator, will interfere with the ability to assess study change in magnetic resonance spectroscopy
4.2.2.28 For lumbar puncture substudy: Thrombocytopenia or other bleeding disorders (including ongoing anticoagulant therapy), suspected increased intracranial pressure or spinal epidural abscess, or any other factor which would increase risk of complications following lumbar puncture