Valproic Acid and Its Effects on HIV Latent Reservoirs

HIV Infections Clinical Trial

Official title:

Use of Valproic Acid to Purge HIV From Resting CD4+ Memory Cells/ A Proof-of-concept Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00289952
• Other study ID #: BMB#05-018 (CTN-205)
• Status: Completed
• Phase: Phase 2
• Start date: June 2006
• Est. completion date: December 2012

Study information

• Verified date: March 2023
• Source: McGill University Health Centre/Research Institute of the McGill University Health Centre
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to examine whether the co-administration of valproic acid (Epival®), with highly active antiretroviral therapy (HAART) can reduce the size of HIV latent reservoirs in infected CD4 cells.

Description:

Participants must be on HAART with a suppressed viral load (< 50 copies/ml) for at least the previous 12 months. They will be randomly assigned to one of two groups, one group will start the valproic acid right away at week 1 for 16 weeks, and the other group will wait until week 17 to add valproic acid to their treatment for 32 weeks. Subjects will be followed every four weeks for one year and evaluated by a variety of assays, all carried out using well-established methods, to assess the main outcome defined by changes in HIV reservoir size measured by the mean frequency of resting CD4 memory cells carrying HIV proviral DNA.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 50
• Est. completion date: December 2012
• Est. primary completion date: December 2012
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

Documented HIV seropositive infection by Western Blot, EIA assays or viral load.

• Aged 18 years old or older.

• Viral load <50 copies/ml for at least the previous 12 months.

• Circulating CD4+ cell count ³ 200 cells/ml.

• Taking HAART.

• Vital signs, physical examination and laboratory results do not exhibit evidence of diseases such as advanced cirrhosis and advanced liver disease (ALT or AST > 5 x upper limit of normal value).

• Karnofsky performance status 80%.

• Subject does not require and agrees not to take, for the duration of the study, any medication that is contraindicated with VPA.

• Willing and able to give informed consent.

• All participants will agree to abstinence or to used effective methods of contraception while on the study.

Exclusion Criteria:

• Pregnant or breast-feeding women.

• Psychiatric or cognitive disturbance or illness that could preclude compliance with the study.

• Current use or use within four weeks prior to the baseline visit, of cytotoxic agents, systemic corticosteroids or any immunomodulatory agents such as intravenous immunoglobulin, or hydroxyurea.

• HIV vaccine within six months of screening visit

• Allergic reaction to VPA.

• Active intravenous drug users.

• History of bleeding disorders.

• Unstable or treated hypertension.

• Past-history of pancreatitis or chronic liver disease (ALT or AST > 5 x upper limit of normal value). However subject co-infected with hepatitis B or C can participate if ALT or AST is < 5 x upper limit of normal value.

• Renal failure (creatinine > 2 x upper limit of normal value).

• Ammonemia (> 2x upper limit of normal value).

• Taking Zidovudine (AZT), or combination of drugs containing AZT like Combivir or Trizivir. However this subject will be asked to switch to another NRTI,at least two weeks prior to Valproic Acid initiation, to become eligible.

• Taking on daily basis: phenytoin, carbamazepine, phenobarbital, warfarin or aspirin.

• Subject has any of the following abnormal laboratory results Hemoglobin < 100 g/L. Absolute neutrophil count < 0.75 x 10 9 cells/L. Platelet count < 50 x 10 9 cells/L.

• Subject suffering from urea cycle disorders.

Related Conditions & MeSH terms

• HIV Infections

Intervention

Drug:
• Valproic Acid
Oral valproic acid twice daily for 16 or 32 weeks. Dosage varies based on plasma levels.
• HAART
As per standard of care.

Locations

Country	Name	City	State
Canada	Actuel Medical Clinic	Montreal	Quebec
Canada	Montreal Chest Institute/Immunodeficiency Clinic	Montreal	Quebec
Canada	Quartier Latin Medical Clinic	Montreal	Quebec
Canada	Ottawa Health Research Institute/Immunodeficiency Clinic	Ottawa	Ontario
Canada	CHUL Ste-Foy	Ste-Foy	Quebec
Canada	BC St-Paul's Hospital/Immunodeficiency Clinic	Vancouver	British Columbia

Sponsors (3)

Lead Sponsor	Collaborator
Jean-Pierre Routy	Canadian Foundation for AIDS Research (CANFAR), CIHR Canadian HIV Trials Network

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To assess the effect of VPA on HIV reservoirs measured by the frequency of resting CD4+ memory cells carrying HIV proviral DNA in peripheral blood of chronically HIV-infected subjects.		16 or 32 weeks
Secondary	To assess the clinical and biological tolerance of VPA in chronically HIV-infected patients with undetectable viral load.		16 or 32 weeks
Secondary	To explore the changes in CD4/CD8 ratio, as the size of reservoir is thought to be inversely correlated with the frequency of resting CD4+ memory cells carrying HIV proviral DNA.		48 weeks
Secondary	To explore the frequency of CD4+ memory cell subsets (Tcm, Tpm and Tem) carrying HIV proviral DNA.		48 weeks
Secondary	To explore level of T-cell activation after VPA intervention.		48 weeks
Secondary	To assess levels of certain cytokines and chemokines, which are involved in T-cell proliferation and differentiation.		48 weeks

External Links

•   Canadian HIV Trials Network (CTN)