Page last updated: 2024-11-04

vorinostat and Acquired Immune Deficiency Syndrome

vorinostat has been researched along with Acquired Immune Deficiency Syndrome in 2 studies

Vorinostat: A hydroxamic acid and anilide derivative that acts as a HISTONE DEACETYLASE inhibitor. It is used in the treatment of CUTANEOUS T-CELL LYMPHOMA and SEZARY SYNDROME.
vorinostat : A dicarboxylic acid diamide comprising suberic (octanedioic) acid coupled to aniline and hydroxylamine. A histone deacetylase inhibitor, it is marketed under the name Zolinza for the treatment of cutaneous T cell lymphoma (CTCL).

Research Excerpts

ExcerptRelevanceReference
"Tamoxifen did not enhance vorinostat-induced HIV transcription (between-arm ratio, 0."3.11Impact of Tamoxifen on Vorinostat-Induced Human Immunodeficiency Virus Expression in Women on Antiretroviral Therapy: AIDS Clinical Trials Group A5366, The MOXIE Trial. ( Aga, E; Archin, N; Bosch, RJ; Chomont, N; Connick, E; Coxen, K; Deeks, S; Dobrowolski, C; Ehui, L; Gandhi, M; Gandhi, RT; Giguel, F; Godfrey, C; Hosey, L; Howell, BJ; Karn, J; Kuritzkes, DR; Ma, Q; Morse, GD; Scully, EP; Sieg, SF; Squires, KE; Starr, K; Tsibris, A; Wu, G, 2022)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (50.00)24.3611
2020's1 (50.00)2.80

Authors

AuthorsStudies
Scully, EP1
Aga, E1
Tsibris, A1
Archin, N1
Starr, K1
Ma, Q1
Morse, GD1
Squires, KE1
Howell, BJ1
Wu, G1
Hosey, L1
Sieg, SF1
Ehui, L1
Giguel, F1
Coxen, K1
Dobrowolski, C1
Gandhi, M1
Deeks, S1
Chomont, N1
Connick, E1
Godfrey, C1
Karn, J1
Kuritzkes, DR1
Bosch, RJ1
Gandhi, RT1
Al-Jabri, AA1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Selective Estrogen Receptor Modulators to Enhance the Efficacy of Viral Reactivation With Histone Deacetylase Inhibitors[NCT03382834]Phase 231 participants (Actual)Interventional2018-04-26Active, not recruiting
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Change From Baseline in Cell-associated HIV-1 RNA in CD4+ T Cells

Baseline is defined as the average of the pre-entry and entry values. Change was calculated as the value of Cell-associated HIV-1 RNA on Day 38 (5 hours post vorinostat) minus the value at baseline. (NCT03382834)
Timeframe: Pre-entry, entry, and Day 38

Interventionlog10 copies/million CD4 cells (Mean)
Arm A: Tamoxifen + Vorinostat0.06
Arm B: Vorinostat Alone0.17

Change From Baseline in Total HIV-1 DNA Levels in CD4+ T Cells

Baseline is defined as the average of the pre-entry and entry values. Change was calculated as the value of Total HIV-1 DNA on Day 38 (5 hours post vorinostat) minus the value at baseline. (NCT03382834)
Timeframe: Pre-entry, entry, and Day 38

Interventionlog10 copies/million CD4 cells (Mean)
Arm A: Tamoxifen + Vorinostat0
Arm B: Vorinostat Alone-0.04

Proportion of Participants With New Grade 3 or Greater Adverse Events

Proportion of participants with new Grade 3 or greater adverse events that are considered definitely, probably, or possibly related to study treatment (as judged by the core protocol team). The DAIDS AE Grading Table (corrected Version 2.1, July 2017) was used. (NCT03382834)
Timeframe: Measured from study entry through Day 65

Interventionproportion of participants (Number)
Arm A: Tamoxifen + Vorinostat0
Arm B: Vorinostat Alone0

Number of Participants With HIV-1 RNA Levels (Measured by Single Copy Assay) Greater or Equal to the Lower Limit of Quantification

Number of participants with HIV-1 RNA levels measured by single copy assay (SCA) greater or equal to the lower limit of quantification (LOQ). The lower limit of quantification for this study was 0.47 copies/mL. (NCT03382834)
Timeframe: Pre-entry, entry, Day 28, Day 35, Day 38 (5 hours post vorinostat), Day 45, Day 65

,
InterventionParticipants (Count of Participants)
Pre-entry SCA >= LOQEntry SCA >=LOQDay 28 SCA >=LOQDay 35 SCA >=LOQDay 38 SCA >=LOQDay 45 SCA >=LOQDay 65 SCA >=LOQ
Arm A: Tamoxifen + Vorinostat10911117910
Arm B: Vorinostat Alone6345545

Trials

1 trial available for vorinostat and Acquired Immune Deficiency Syndrome

ArticleYear
Impact of Tamoxifen on Vorinostat-Induced Human Immunodeficiency Virus Expression in Women on Antiretroviral Therapy: AIDS Clinical Trials Group A5366, The MOXIE Trial.
    Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2022, 10-12, Volume: 75, Issue:8

    Topics: Acquired Immunodeficiency Syndrome; CD4-Positive T-Lymphocytes; DNA; Estrogen Receptor alpha; Female

2022

Other Studies

1 other study available for vorinostat and Acquired Immune Deficiency Syndrome

ArticleYear
Forcing the enemy to come out and surrender: a strategy for an AIDS cure.
    AIDS research and human retroviruses, 2015, Volume: 31, Issue:1

    Topics: Acquired Immunodeficiency Syndrome; Anti-HIV Agents; Antiretroviral Therapy, Highly Active; Depsipep

2015