ARVs and ART – looking to the future Sharon R Lewin Professor and Head, Department of Infectious Diseases, Monash University and Alfred Hospital Co-head,

Slides:



Advertisements
Similar presentations
International Antiviral SocietyUSA Panel
Advertisements

Aging, Inflammation, and Organ Damage in HIV+ Patients Jean-Pierre Routy, MD Graeme Moyle, MD Bill Powderly, MD Philippe Morlat, MD.
A daily dose of 400 mg efavirenz (EFV) is non-inferior to the standard 600 mg dose: week 48 data from the ENCORE1 study, a randomised, double-blind, placebo.
IAS–USA Managing Antiretroviral Failure in 2012 Jennifer Hoy, MD Professor of Medicine Director, HIV Medicine The Alfred Hospital FINAL: Presented.
The new guidelines Dr Francois Venter Reproductive Health and HIV Research Unit University of the Witwatersrand Feb 2010.
New Antiretrovirals for the Treatment of HIV. Convenience, tolerability, simplicity New & Investigational Agents.
Developing child-appropriate formulations: what is in the research pipeline for paediatric ARVS? July 17, 2011 Challenges in the Development & Procurement.
Switch to EVG/c/FTC/TDF  STRATEGY-PI Study  STRATEGY-NNRTI Study.
Initiating Antiretroviral Therapy in Treatment-Naive Patients Charles B. Hicks, MD Associate Professor of Medicine, Division of Infectious Diseases and.
ANTIRETROVIRAL THERAPY Dr. Samuel Mwaniki (BPharm., MSc TID, UoN) University of Nairobi ISO 9001: Certified
Slide 1 of 11 From CB Hicks, MD, at Chicago, IL: May 20, 2013, IAS-USA. IAS–USA Charles B. Hicks, MD Professor of Medicine Duke University Medical Center.
20th International AIDS Conference; July 20-25, 2014; Melbourne, Australia DTG-Based Regimens Are Active in INI-Naive Patients With a History of NRTI Resistance.
Cardiovascular Complications of HIV Mark Boyd MD, FRACP The Kirby Institute for infection and immunity in society 7 th IAS Conference Kuala Lumpur, Malaysia.
N ORTHWEST A IDS E DUCATION AND T RAINING C ENTER CROI 2015: Treatment and Cure Highlights Shireesha Dhanireddy Robert Harrington March 17, 2014 No financial.
Hepatitis web study Hepatitis web study Ledipasvir-Sofosbuvir in GT-1 and HIV Coinfection NIAID ERADICATE Trial Phase 2a Treatment Naïve and Treatment.
Hepatitis web study Hepatitis web study Ledipasvir-Sofosbuvir in GT1 or GT4 and HIV Coinfection ION-4 Phase 3 Treatment Naïve and Treatment Experienced.
Can dose-optimization trials be conducted ethically in low-income countries? Dr Andrew Hill World AIDS Conference, Melbourne, Australia July 2014 [TUWS1104]
Presented by: Siti Rohaizah bt Othman. Arv DRUGS AVAILABLE IN UMMC Combivir (Lamivudine + Zidovudine) Stocrin (Efavirenz 600mg) Kaletra (Lopinavir 200mg.
Long Term Management of HIV Infection in Aging Adults: Current Challenges, Future Strategies Andrew Zolopa, MD Stanford University.
Effects of nucleoside analogues versus ritonavir boosted protease inhibitors on lipid levels – analysis of 12 clinical trials in 4231 antiretroviral naïve.
Slide 1 of 9 From J Marrazzo, MD, at Los Angeles, CA: April 22, 2013, IAS-USA. IAS–USA Jeanne Marrazzo, MD, MPH Professor of Medicine University of Washington.
Is monitoring for CD4 counts still needed for the management of patients with long- term HIV RNA suppression? Andrew Hill, Liverpool University, UK.
Comparison of PI vs PI  ATV vs ATV/r BMS 089  LPV/r mono vs LPV/r + ZDV/3TC MONARK  LPV/r QD vs BID M M A5073  LPV/r + 3TC vs LPV/r + 2.
Phase 2 of new ARVs  Fostemsavir, prodrug of temsavir (attachment inhibitor) –AI Study  TAF (TFV prodrug) –Study –Study  Doravirine.
2009 Recommendations for Antiretroviral Therapy in Adults and Adolescents Summary of WHO Rapid Advice December 2009 Source: WHO HIV/AIDS Department.
1 Review of Antiretroviral Therapy in Adults HAIVN Harvard Medical School AIDS Initiative in Vietnam.
Hepatitis web study Hepatitis web study Ledipasvir-Sofosbuvir in GT1 or GT4 and HIV Coinfection ION-4 Phase 3 Treatment Naïve and Treatment Experienced.
Emerging comorbidities in the setting of long- term virological suppression Antonella Castagna San Raffaele Scientific Institute, Milan.
1 Introduction to ARV Therapy HAIVN Harvard Medical School AIDS Initiative in Vietnam.
Are we most likely to cure HIV with gene therapy? Sharon R Lewin Director, Infectious Disease Unit, Alfred Hospital Professor, Department of Medicine,
Update on HIV Therapy Elly T Katabira, FRCP Department of Medicine Makerere University Medical School Scaling up Treatment Programs: Issues, Challenges.
Switch to DRV/r monotherapy  MONOI  MONET  PROTEA  DRV600.
The role of treatment versus disease in causing premature non-AIDS morbidity Judith S. Currier, MD University of California, Los Angeles.
Comparison of NNRTI vs PI/r  EFV vs LPV/r vs EFV + LPV/r –A5142 –Mexican Study  NVP vs ATV/r –ARTEN  EFV vs ATV/r –A5202.
Clinical development programme for Second-Line treatment Anton Pozniak World AIDS Conference, July 2014.
Joel E. Gallant, MD, MPH Medical Director, Specialty Services Southwest CARE Center Santa Fe, New Mexico State-of-the-ART in Antiretroviral Management.
Efficacy and safety of dolutegravir (DTG) in treatment-naïve subjects
1 Antiretroviral Regimen and Pharmacogenetic Determinants of Tenofovir-associated Change in Creatinine Clearance in ACTG Protocol A5142 (NWCS 291) Miguel.
SAILING Efficacy and safety of dolutegravir (DTG) in treatment- experienced INI-naïve patients DK/DLG/0041/14c September 2015.
The Impact of Darunavir/ritonavir (DRV/r) & Raltegravir (RAL) in the Clinic: A New Era for Treatment-Experienced Patients? M. Mugavero 1, H. Lin 1, J.
ACTG 5142: First-line Antiretroviral Therapy With Efavirenz Plus NRTIs Has Greater Antiretroviral Activity Than Lopinavir/Ritonavir Plus NRTIs Slideset.
First-Line Treatment of HIV Infection With Either NNRTI- or PI-Based Regimens Effective for Long-term Disease Control Slideset on: MacArthur RD, Novak.
Roy M. Gulick, MD, MPH Gladys and Roland Harriman Professor of Medicine Chief, Division of Infectious Diseases Weill Medical College of Cornell University.
NEXT STEPS IN THE GLOBAL TREATMENT SIMPLIFICATION AGENDA THE ROLE OF PARTNERSHIPS Nathan Ford Department HIV and Global Hepatitis Programme WHO, Geneva.
Roy M. Gulick, MD, MPH Gladys and Roland Harriman Professor of Medicine Chief, Division of Infectious Diseases Weill Medical College of Cornell University.
Phase 3 Treatment-Naïve and Treatment-Experienced
Novel Antiretroviral Studies and Strategies
Switch to PI/r monotherapy
Antiretroviral Therapy (ART)
Optimizing Antiretorviral Therapy for Long-Term HIV Care
OVERVIEW OF PREVENTING MOTHER TO CHILD TRANSMISSION OF HIV
RAL + MVC + DRV/r + TDF-FTC
EFV versus ATV + RTV, both with ABC-3TC or TDF-FTC ACTG 5202
TREATMENT OF HIV.
TDF-FTC QD + Raltegravir BID TDF-FTC QD + Lopinavir-ritonavir QD
Switch to RPV-TDF-FTC from Ritonavir-boosted PI Regimen SPIRIT STUDY
Lopinavir-ritonavir mg BID (n = 354)
Sofosbuvir-Velpatasvir in HIV-HCV Coinfected Patients ASTRAL-5
Once Daily Etravirine versus Efavirenz in Treatment-Naive SENSE Trial
Dolutegravir versus Raltegravir in Treatment Experienced SAILING Study
Atazanavir + ritonavir vs. Lopinavir-ritonavir CASTLE Study
Optimising ART sub-Saharan Africa
Advances in HIV Care.
PrEP Pre-Exposure Prophylaxis
Next Generation Capsid Inhibitor: GS–CA1
Why Dolutegravir? Daniel R. Kuritzkes, M.D.
Phase 3 Treatment Naïve and Treatment Experienced HIV Coinfection
Switch to DRV/r monotherapy
Comparison of NNRTI vs PI/r
Dolutegravir in PEPFAR
Presentation transcript:

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

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

cheaper and better antiretrovirals

Strategies to reduce cost of current ARVs  Optimising the active pharmaceutical ingredient (API) –Optimise material sourcing –Change in manufacturing process –Improve bioavailability  Pharmaco-enhancement  Extension of shelf-life  Reduce dose Crawford et al., Lancet Infect Dis 2012; 12:550; Conference on Antiretroviral Dose Optimisation (CADO), 2010

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

Lower doses can be effective, reduce toxicities…and reduce cost DrugDoses studiedOutcomeStudy NNRTI Efavirenz600mg vs 400mg vs 200mg No difference in %<400 c/ml Hicks Riplivarine150mg vs 75 mg vs 25mg All doses non inferior to EFV Pozniak Protease inhibitors LPV/r400/100 vs 200/100 mg Improved outcomes for low dose Murphy Integrase inhibitors Raltegravir600 vs 400 vs 200 vs 100 mg HIV RNA < 50 c/ml in 85%, 83%, 88% and 88% Markowitz

New ARVs in development NRTINNRTIPIEntry InhInSTI Phase 3 TAF cenicrivirocdolutegravir Phase 2apricitabine DAPD dexelvucitabine festinavir BILR 355 MK-1439 BMS ibalizumab PF GSK744 Phase 1/2amdoxovir elvucitabine TMC HGS004 Phase 1RDEA 806CTP-298 CTP-518 PPL-100 SPI-256 SCH VIR-576 BI INH-1001 Gulick, 20 th CROI, Atlanta, GA, March 2013

Tenofovir alenofenamide (TAF): reduced renal toxicity and cost Zolopa CROI 2013, Atlanta, GA # 99LB % HIV-1 RNA <50 c/mL Time (Weeks) TAF/FTC/EVG/c 88% (n=112) TDF/FTC/EVG/c 90% (n=58) Change in serum creatinine at Week 24 TAF mg/dL TDF mg/dL (p=0.02) TAF/FTC/EVG/COBI Rx-naïve, VL >5000, CD4 >50 (N=170)

New technologies for delivery of ARVs  Nanotechnology –Efavirenz 300mg –Pediatric LPV/r in development  Injectables, implants, slow release –GSK744 + rilpivarine LA –GSK NRTI (Latte study) –Vaginal rings e.g., dapivirine / maraviroc  Multipurpose prevention technologies –HIV + STI + pregnancy

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

reduce long term morbidity

Increased age-related complications on ART Frieberg et al., JAMA Internal Med 2013 Increased risk of AMI in HIV compared to HIV uninfected HR = 1.48 (CI = 1.27 – 1.72) Further increase HR if CD4 500 Mean AMI events per 1000 person years N=82,459; Veterans Ageing Cohort Study Virtual Cohort

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

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 cART toxicity Persistent inflammation (immune activation) Non-AIDS events (e.g. smoking)

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

the very distant future

HIV cure is rare and possible – but a very long term goal THE VISCONTI PATIENTS The Mississippi baby The Berlin Patient

Acknowledgements  The Alfred Hospital, Melbourne –Julian Elliott –Jennifer Hoy –Edwina Wright  Elsewhere –Steve Deeks –Diane Havlir –Trip Gulich –Judith Currier –Andrew Ball –Adeeba Kamarulzaman