ARV and ART: looking to the future

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ARVs and ART – looking to the future Sharon R Lewin Professor and Head, Department of Infectious Diseases, Monash University and Alfred Hospital Co-head, Centre for Biomedical Research, Burnet Institute, Melbourne, Australia 7 th IAS Conference on Pathogenesis, Treatment and Prevention, Kuala Lumpur, 30 th June – 3 rd July, 2013

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Page 1: ARV and ART: looking to the future

ARVs and ART – looking to the futureSharon R LewinProfessor and Head, Department of Infectious Diseases, Monash University and Alfred HospitalCo-head, Centre for Biomedical Research, Burnet Institute, Melbourne, Australia

7th IAS Conference on Pathogenesis, Treatment and Prevention, Kuala Lumpur, 30th June – 3rd July, 2013

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ARV and ART: looking to the future

Better antiretrovirals–Reduce cost–Reduce toxicity–Enhance durability of control

Reduce long term morbidity

The very distant future

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cheaper and better antiretrovirals

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Strategies to reduce cost of current ARVsOptimising the active pharmaceutical

ingredient (API)– Optimise material sourcing– Change in manufacturing process– Improve bioavailability

Pharmaco-enhancementExtension of shelf-lifeReduce dose

Crawford et al., Lancet Infect Dis 2012; 12:550; Conference on Antiretroviral Dose Optimisation (CADO), 2010

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New source of raw material Mg tert-butoxide reduces cost of TDF

Similar strategies currently being evaluated for efavirenz, ATZ/r, DRV/r

Crawford et al., Lancet Infect Dis 2012; 12:550

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Lower doses can be effective, reduce toxicities…and reduce costDrug Doses studied Outcome StudyNNRTIEfavirenz 600mg vs 400mg

vs 200mgNo difference in %<400 c/ml

Hicks

Riplivarine 150mg vs 75 mg vs 25mg

All doses non inferior to EFV

Pozniak

Protease inhibitorsLPV/r 400/100 vs

200/100 mgImproved outcomes for low dose

Murphy

Integrase inhibitorsRaltegravir 600 vs 400 vs

200 vs 100 mgHIV RNA < 50 c/ml in 85%, 83%, 88% and 88%

Markowitz

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New ARVs in development

NRTI NNRTI PI Entry Inh InSTI

Phase 3 TAF cenicriviroc dolutegravir

Phase 2 apricitabine DAPD dexelvucitabinefestinavir

BILR 355 MK-1439

BMS-663068 ibalizumab PF-232798

GSK744

Phase 1/2 amdoxovir elvucitabine

TMC 310911

HGS004

Phase 1 RDEA 806 CTP-298 CTP-518 PPL-100 SPI-256

SCH532706 VIR-576

BI 224436 INH-1001

Gulick, 20th CROI, Atlanta, GA, March 2013

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Tenofovir alenofenamide (TAF): reduced renal toxicity and cost

Zolopa CROI 2013, Atlanta, GA # 99LB

0102030405060708090

100

2 4 8 12 16 24

% H

IV-1

RN

A <5

0 c/

mL

Time (Weeks)

TAF/FTC/EVG/c 88% (n=112)

TDF/FTC/EVG/c 90% (n=58)

Change in serum creatinine at Week 24TAF +0.07 mg/dL

TDF +0.12 mg/dL (p=0.02)

TAF/FTC/EVG/COBI

Rx-naïve, VL >5000, CD4 >50 (N=170)

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New technologies for delivery of ARVsNanotechnology

– Efavirenz 300mg – Pediatric LPV/r in development

Injectables, implants, slow release– GSK744 + rilpivarine LA– GSK744 + 2NRTI (Latte study)– Vaginal rings e.g., dapivirine / maraviroc

Multipurpose prevention technologies– HIV + STI + pregnancy

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Long and short term priorities to improve ARVs First-line

– fixed-dose combination regimens that are equally or more potent and more durable and affordable than TDF/XTC/EFV

Post Treatment –failure – fixed dose boosted, dose-optimized darunavir in replacing atazanavir or

lopinavir as the protease inhibitor of choice– A one pill once daily second-line regimen.– Studies of reduced-dose darunavir/ritonavir (DRV/r),

Enhancing Trial Participant Criteria– including girls and women of reproductive age, TB co-infection, and

comorbidities (such as hypertension).

Longer Term Research Priorities– oral and injectable long-acting drugs (including GSK744 and TMC278)

as well as nano-formulations and implantable devices.

CADO2 report, South Africa, April 2013

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reduce long term morbidity

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Increased age-related complications on ART

Frieberg et al., JAMA Internal Med 2013

Increased risk of AMI in HIV compared to HIV uninfectedHR = 1.48 (CI = 1.27 – 1.72)

Further increase HR if CD4<200 or HIV RNA>500

Mea

n A

MI e

vent

s pe

r 1

000

pers

on y

ears

40-49 years 50-59 years 60-69 years0

1

2

3

4

5

6

2

3.9

5

1.52.2

3.3

HIV+ HIV-

N=82,459; Veterans Ageing Cohort Study Virtual Cohort

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HIV and aging in Africa

Mills et al., N Engl J Med 2012; 366:14

In 2040, the number of persons over 50 years of age living with HIV is expected to be 9 million

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Lifestyle

Etiology of non-AIDS-related events

Non-AIDS-related events are more common in HIV disease, even after adjustment for age, cART exposure and traditional risk factors

Deeks SG, Phillips AN. Br Med J 2009;338:a3172

cARTtoxicity

Persistentinflammation(immune activation)

Non-AIDS events

(e.g. smoking)

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Prevention of non AIDS events needs a different model of care Lifestyle modifications

– Reduce smoking, healthy diet, exercise Reduce modifiable risk factors

– Assessment of blood pressure, glucose and lipids

Counselling and screening for common cancers

Enhance CD4 recovery and reduce inflammation

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the very distant future

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HIV cure is rare and possible – but a very long term goal

THE VISCONTI PATIENTS The Mississippi

baby

The Berlin Patient

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Acknowledgements The Alfred Hospital,

Melbourne– Julian Elliott – Jennifer Hoy– Edwina Wright

Elsewhere– Steve Deeks– Diane Havlir– Trip Gulich– Judith Currier– Andrew Ball– Adeeba Kamarulzaman

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