Jayachandran, Priya

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  • Jayachandran, Priya (2)
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Author's Bibliography

Characterizing HIV-Preventive, Plasma Tenofovir Concentrations-A Pooled Participant-level Data Analysis From Human Immunodeficiency Virus Preexposure Prophylaxis (PrEP) Clinical Trials

Garcia-Cremades, Maria; Vučićević, Katarina; Hendrix, Craig W; Jayachandran, Priya; Jarlsberg, Leah; Grant, Robert; Celum, Connie L.; Martin, Michael; Baeten, Jared M.; Marrazzo, Jeanne; Anderson, Peter; Choopanya, Kachit; Vanichseni, Suphak; Glidden, David V.; Savić, Radojka M.

(Oxford University Press, 2022)

TY  - JOUR
AU  - Garcia-Cremades, Maria
AU  - Vučićević, Katarina
AU  - Hendrix, Craig W
AU  - Jayachandran, Priya
AU  - Jarlsberg, Leah
AU  - Grant, Robert
AU  - Celum, Connie L.
AU  - Martin, Michael
AU  - Baeten, Jared M.
AU  - Marrazzo, Jeanne
AU  - Anderson, Peter
AU  - Choopanya, Kachit
AU  - Vanichseni, Suphak
AU  - Glidden, David V.
AU  - Savić, Radojka M.
PY  - 2022
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/4338
AB  - Background. Daily dosing of tenofovir disoproxil fumarate, with or without emtricitabine, has high efficacy in preventing human immunodeficiency virus (HIV) infection when individuals are adherent. The target protective plasma concentration of tenofovir (TFV), however, is not fully understood. The aim of this study is to estimate the protective TFV plasma concentration. Methods. Participant data from TFV-based daily oral and topical active arms of phase 3 trials (iPrEx, VOICE, and Partners PrEP) were pooled (n = 2950). Individual specific risk scores (low and high risk) of acquiring HIV, based on an earlier placebo analysis, were created. Longitudinal TFV pharmacokinetics (PK), HIV outcome, individual risk scores and the effect of sex at birth data were integrated and analyzed using non-linear mixed effects models. Results. Around 50% of the individuals were estimated to be adherent, which differed from self-reported adherence (≏90%) and large variation between longitudinal adherence patterns were identified. Following oral administration, the estimated protective TFV trough concentration was substantially higher in high-risk females (45.8 ng/mL) compared with high-risk males (16.1 ng/mL) and to low-risk individuals (≏7.5 ng/mL). Dosing simulations indicated that high-risk women require full adherence to maintain protective levels. Conclusions. Using the largest PK-HIV outcome database to date, we developed a population adherence-PK-risk-outcome model. Our results indicate that high-risk females need higher levels of plasma TFV to achieve HIV protection compared with males. HIV protection exceeds 90% in all populations if daily adherence is achieved.
PB  - Oxford University Press
T2  - Clinical Infectious Diseases
T1  - Characterizing HIV-Preventive, Plasma Tenofovir Concentrations-A Pooled Participant-level Data Analysis From Human Immunodeficiency Virus Preexposure Prophylaxis (PrEP) Clinical Trials
VL  - 75
IS  - 11
SP  - 1873
EP  - 1882
DO  - 10.1093/cid/ciac313
ER  - 
@article{
author = "Garcia-Cremades, Maria and Vučićević, Katarina and Hendrix, Craig W and Jayachandran, Priya and Jarlsberg, Leah and Grant, Robert and Celum, Connie L. and Martin, Michael and Baeten, Jared M. and Marrazzo, Jeanne and Anderson, Peter and Choopanya, Kachit and Vanichseni, Suphak and Glidden, David V. and Savić, Radojka M.",
year = "2022",
abstract = "Background. Daily dosing of tenofovir disoproxil fumarate, with or without emtricitabine, has high efficacy in preventing human immunodeficiency virus (HIV) infection when individuals are adherent. The target protective plasma concentration of tenofovir (TFV), however, is not fully understood. The aim of this study is to estimate the protective TFV plasma concentration. Methods. Participant data from TFV-based daily oral and topical active arms of phase 3 trials (iPrEx, VOICE, and Partners PrEP) were pooled (n = 2950). Individual specific risk scores (low and high risk) of acquiring HIV, based on an earlier placebo analysis, were created. Longitudinal TFV pharmacokinetics (PK), HIV outcome, individual risk scores and the effect of sex at birth data were integrated and analyzed using non-linear mixed effects models. Results. Around 50% of the individuals were estimated to be adherent, which differed from self-reported adherence (≏90%) and large variation between longitudinal adherence patterns were identified. Following oral administration, the estimated protective TFV trough concentration was substantially higher in high-risk females (45.8 ng/mL) compared with high-risk males (16.1 ng/mL) and to low-risk individuals (≏7.5 ng/mL). Dosing simulations indicated that high-risk women require full adherence to maintain protective levels. Conclusions. Using the largest PK-HIV outcome database to date, we developed a population adherence-PK-risk-outcome model. Our results indicate that high-risk females need higher levels of plasma TFV to achieve HIV protection compared with males. HIV protection exceeds 90% in all populations if daily adherence is achieved.",
publisher = "Oxford University Press",
journal = "Clinical Infectious Diseases",
title = "Characterizing HIV-Preventive, Plasma Tenofovir Concentrations-A Pooled Participant-level Data Analysis From Human Immunodeficiency Virus Preexposure Prophylaxis (PrEP) Clinical Trials",
volume = "75",
number = "11",
pages = "1873-1882",
doi = "10.1093/cid/ciac313"
}
Garcia-Cremades, M., Vučićević, K., Hendrix, C. W., Jayachandran, P., Jarlsberg, L., Grant, R., Celum, C. L., Martin, M., Baeten, J. M., Marrazzo, J., Anderson, P., Choopanya, K., Vanichseni, S., Glidden, D. V.,& Savić, R. M.. (2022). Characterizing HIV-Preventive, Plasma Tenofovir Concentrations-A Pooled Participant-level Data Analysis From Human Immunodeficiency Virus Preexposure Prophylaxis (PrEP) Clinical Trials. in Clinical Infectious Diseases
Oxford University Press., 75(11), 1873-1882.
https://doi.org/10.1093/cid/ciac313
Garcia-Cremades M, Vučićević K, Hendrix CW, Jayachandran P, Jarlsberg L, Grant R, Celum CL, Martin M, Baeten JM, Marrazzo J, Anderson P, Choopanya K, Vanichseni S, Glidden DV, Savić RM. Characterizing HIV-Preventive, Plasma Tenofovir Concentrations-A Pooled Participant-level Data Analysis From Human Immunodeficiency Virus Preexposure Prophylaxis (PrEP) Clinical Trials. in Clinical Infectious Diseases. 2022;75(11):1873-1882.
doi:10.1093/cid/ciac313 .
Garcia-Cremades, Maria, Vučićević, Katarina, Hendrix, Craig W, Jayachandran, Priya, Jarlsberg, Leah, Grant, Robert, Celum, Connie L., Martin, Michael, Baeten, Jared M., Marrazzo, Jeanne, Anderson, Peter, Choopanya, Kachit, Vanichseni, Suphak, Glidden, David V., Savić, Radojka M., "Characterizing HIV-Preventive, Plasma Tenofovir Concentrations-A Pooled Participant-level Data Analysis From Human Immunodeficiency Virus Preexposure Prophylaxis (PrEP) Clinical Trials" in Clinical Infectious Diseases, 75, no. 11 (2022):1873-1882,
https://doi.org/10.1093/cid/ciac313 . .
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A Mechanistic In Vivo/Ex Vivo Pharmacokinetic-Pharmacodynamic Model of Tenofovir for HIV Prevention

Jayachandran, Priya; Garcia-Cremades, Maria; Vučićević, Katarina; Bumpus, Namandjé; Anton, Peter; Hendrix, Craig; Savić, Radojka

(American Society for Clinical Pharmacology and Therapeutics, 2021)

TY  - JOUR
AU  - Jayachandran, Priya
AU  - Garcia-Cremades, Maria
AU  - Vučićević, Katarina
AU  - Bumpus, Namandjé
AU  - Anton, Peter
AU  - Hendrix, Craig
AU  - Savić, Radojka
PY  - 2021
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3785
AB  - Defining tissue and plasma-specific prophylactic drug concentrations is central to pre-exposure prophylaxis product development for sexual transmission of HIV-1. Pharmacokinetic (PK) data from study RMP-02/MTN-006 comparing single dose oral tenofovir disoproxil fumarate with single and multiple dose rectal tenofovir (TFV) gel administration in HIV-1 seronegative adults was used to construct a multicompartment plasma-rectal tissue population PK model for TFV and tenofovir-diphosphate (TFVdp) in plasma and rectal tissue. PK data were collected in five matrices: TFV (plasma, rectal tissue homogenate), TFVdp (peripheral blood mononuclear cells, rectal mononuclear cells (MMCs), rectal tissue homogenate). A viral growth compartment and a delayed effect compartment for p24 antigen expression measured from an ex vivo explant assay described HIV-1 infection and replication. Using a linear PK/pharmacodynamic model, MMC TFVdp levels over 9,000 fmol/million cells in the explant assay provided apparent viral replication suppression down to 1%. Parameters were estimated using NONMEM version 7.4.
PB  - American Society for Clinical Pharmacology and Therapeutics
T2  - CPT: Pharmacometrics and Systems Pharmacology
T1  - A Mechanistic In Vivo/Ex Vivo Pharmacokinetic-Pharmacodynamic Model of Tenofovir for HIV Prevention
VL  - 10
SP  - 179
EP  - 187
DO  - 10.1002/psp4.12583
ER  - 
@article{
author = "Jayachandran, Priya and Garcia-Cremades, Maria and Vučićević, Katarina and Bumpus, Namandjé and Anton, Peter and Hendrix, Craig and Savić, Radojka",
year = "2021",
abstract = "Defining tissue and plasma-specific prophylactic drug concentrations is central to pre-exposure prophylaxis product development for sexual transmission of HIV-1. Pharmacokinetic (PK) data from study RMP-02/MTN-006 comparing single dose oral tenofovir disoproxil fumarate with single and multiple dose rectal tenofovir (TFV) gel administration in HIV-1 seronegative adults was used to construct a multicompartment plasma-rectal tissue population PK model for TFV and tenofovir-diphosphate (TFVdp) in plasma and rectal tissue. PK data were collected in five matrices: TFV (plasma, rectal tissue homogenate), TFVdp (peripheral blood mononuclear cells, rectal mononuclear cells (MMCs), rectal tissue homogenate). A viral growth compartment and a delayed effect compartment for p24 antigen expression measured from an ex vivo explant assay described HIV-1 infection and replication. Using a linear PK/pharmacodynamic model, MMC TFVdp levels over 9,000 fmol/million cells in the explant assay provided apparent viral replication suppression down to 1%. Parameters were estimated using NONMEM version 7.4.",
publisher = "American Society for Clinical Pharmacology and Therapeutics",
journal = "CPT: Pharmacometrics and Systems Pharmacology",
title = "A Mechanistic In Vivo/Ex Vivo Pharmacokinetic-Pharmacodynamic Model of Tenofovir for HIV Prevention",
volume = "10",
pages = "179-187",
doi = "10.1002/psp4.12583"
}
Jayachandran, P., Garcia-Cremades, M., Vučićević, K., Bumpus, N., Anton, P., Hendrix, C.,& Savić, R.. (2021). A Mechanistic In Vivo/Ex Vivo Pharmacokinetic-Pharmacodynamic Model of Tenofovir for HIV Prevention. in CPT: Pharmacometrics and Systems Pharmacology
American Society for Clinical Pharmacology and Therapeutics., 10, 179-187.
https://doi.org/10.1002/psp4.12583
Jayachandran P, Garcia-Cremades M, Vučićević K, Bumpus N, Anton P, Hendrix C, Savić R. A Mechanistic In Vivo/Ex Vivo Pharmacokinetic-Pharmacodynamic Model of Tenofovir for HIV Prevention. in CPT: Pharmacometrics and Systems Pharmacology. 2021;10:179-187.
doi:10.1002/psp4.12583 .
Jayachandran, Priya, Garcia-Cremades, Maria, Vučićević, Katarina, Bumpus, Namandjé, Anton, Peter, Hendrix, Craig, Savić, Radojka, "A Mechanistic In Vivo/Ex Vivo Pharmacokinetic-Pharmacodynamic Model of Tenofovir for HIV Prevention" in CPT: Pharmacometrics and Systems Pharmacology, 10 (2021):179-187,
https://doi.org/10.1002/psp4.12583 . .
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