New Phase 3 AMBER study data continues to demonstrate high rates of virologic suppression at 96 weeks in ART-naïve adults with HIV-1 when treated with SYMTUZA®[1]
GLASGOW, UK I October 30, 2018 I The Janssen Pharmaceutical Companies of Johnson & Johnson unveiled new 96-week data for SYMTUZA® (darunavir 800 mg, cobicistat 150 mg, emtricitabine 200 mg and tenofovir alafenamide 10 mg; (D/C/F/TAF)), a once-daily single-tablet regimen (STR) for the treatment of human immunodeficiency virus type 1 (HIV-1) infection in treatment-naïve and certain virologically suppressed adults, at HIV Glasgow in Scotland.
These 96-week data, which follow on from the earlier 48-week results, reinforce the long-term safety, efficacy and tolerability profile of SYMTUZA® as a treatment for antiretroviral treatment (ART)-naïve adults with HIV-1.1,2 Results demonstrated that a high proportion of ART-naïve adults with HIV-1 (85%, 308/362) achieved virologic suppression (viral load <50 c/mL; FDA-snapshot) at 96 weeks when treated with SYMTUZA®. There was a low virologic failure rate (6%, 20/362; viral load of ≥50 c/mL; FDA-snapshot) in patients treated with SYMTUZA® and no darunavir, primary protease inhibitor or tenofovir resistance-associated mutations emerged in any patient. As previously reported, only 1 patient receiving SYMTUZA® developed a nucleoside reverse transcriptase inhibitor resistance-associated mutation (M184I/V) through week 48. In the current analysis through 96 weeks, only 1 additional patient receiving SYMTUZA® developed a nucleoside reverse transcriptase inhibitor resistance-associated mutation to emtricitabine (M184V).1
Efficacy and safety results were consistent with the 48-week results in the SYMTUZA® group presented at the 2017 European AIDS Clinical Society (EACS) Conference and published in the journal AIDS.1,2,3 SYMTUZA® was well-tolerated with 3% (10/362) of people experiencing adverse event (AE)-related discontinuations over 96 weeks and 3% (11/362) of people experiencing a grade 3 or 4 study drug-related AE. The most common study drug-related AEs (all grades, ≥5% of adults) in the extension period were diarrhea, rash and nausea. Bone, renal and lipid safety results were consistent with known tenofovir alafenamide and cobicistat profiles.1
“The 96-week AMBER data further demonstrate the importance of SYMTUZA® as a treatment option for adults new to HIV therapy who may benefit from a single-tablet regimen that offers the protective barrier to resistance of darunavir along with the tolerability profile of TAF,” said Joseph Eron, M.D., Professor of Medicine and Director, Clinical Core, University of North Carolina Center for AIDS Research, Chapel Hill, NC.* “Based on the DHHS guidelines, darunavir-based regimens are a recommended option in situations where clinicians may not have all genotypic resistance test results, when patients may be at risk for sub-optimal adherence or in rapid initiation scenarios.”
The U.S. Department of Health and Human Services (DHHS) guidelines recommend darunavir for patients who may have suboptimal adherence and face the risk of developing HIV drug resistance, which is when a medication stops working to fight the virus, or for those who may require the rapid initiation of ART before full blood work is available.4 The International Antiviral Society (IAS)-USA guidelines also recommend darunavir-based regimens in rapid initiation scenarios.5
“Long-term AMBER results further build on the growing clinical data set that provides additional support for SYMTUZA® as a treatment option for patients who are starting therapy,” said Richard Nettles, M.D., Vice President, Medical Affairs, Janssen Therapeutics, Janssen Scientific Affairs, LLC. “At Janssen, we are building on our 25-year heritage in HIV and remain committed to the research and development of transformational medicines and solutions that span the continuum of HIV care to address real-world clinical challenges, combat HIV drug resistance and meet the diverse needs of those living with HIV.”
SYMTUZA® was approved by the U.S. Food & Drug Administration (FDA) in July 2018 for treatment-naïve and certain virologically suppressed adults. The approval was based on the results from the two pivotal Phase 3 studies, EMERALD and AMBER.2,3,6 96-week results from the Phase 3 EMERALD trial were recently presented at IDWeek 2018, in San Francisco, CA.7
SYMTUZA® has also been approved by the European Commission (EC) and Health Canada for the treatment of HIV-1 infection in adults and adolescents 12 years of age and older with body weight of at least 40 kg. European approval allows Janssen to market SYMTUZA® in all member states of the European Union and the European Economic Area. Janssen plans additional regulatory filings in other markets worldwide.
SYMTUZA® does not cure or prevent HIV-1 or AIDS.
Please see Important Safety Information below, including Boxed Warning for SYMTUZA®.
To learn more about Janssen’s commitment to the prevention and treatment of HIV, please visit jnj.com/HIV.
About the AMBER clinical trial1,2,3
AMBER is a Phase 3 randomized, double-blind, active-controlled, international, multi-center, non-inferiority study designed to assess the safety and efficacy of SYMTUZA® versus the control in HIV-1 treatment-naïve patients. The control was comprised of two separate medications – darunavir/cobicistat plus emtricitabine/tenofovir disoproxil fumarate – and patients were randomly assigned (362 SYMTUZA®; 363 control). The primary endpoint was non-inferiority of the single-tablet regimen versus the control regarding the proportion of patients that achieved viral suppression at Week 48 (viral load of less than 50 c/mL per FDA-snapshot analysis). Reaching suppression of viral load (or the amount of HIV virus in the blood) is a key treatment goal for people living with HIV. Based on the results of the primary analysis, patients were eligible to receive treatment with SYMTUZA® during an open-label single-group treatment phase up to Week 96.
48-week data have been previously reported.2,3 At Week 96, a high proportion of patients in the SYMTUZA® arm (85%, 308/362) achieved virologic suppression. Viral load of ≥50 c/mL per the FDA snapshot at Week 96 occurred in 20/362 (6%) patients in the SYMTUZA® arm. No darunavir, primary protease inhibitor, or tenofovir resistance-associated mutations emerged in any patient. Through 96 weeks, only two patients receiving SYMTUZA® developed a nucleoside reverse transcriptase inhibitor resistance-associated mutation to emtricitabine (M184I/V).1 SYMTUZA® was well-tolerated with few serious adverse events (n=39, 11%) or adverse event-related discontinuations (n=10, 3%), and no deaths occurred. Bone, renal and lipid safety were consistent with known tenofovir and cobicistat profiles, with a small change in TC/HDL-C ratio.1 Efficacy and safety results in the SYMTUZA® arm were consistent with the 48-week results.1
WHAT IS SYMTUZA®?
SYMTUZA® is a prescription medicine that is used without other antiretroviral medicines to treat Human Immunodeficiency Virus-1 (HIV-1) infection in adults who:
- have not received anti-HIV-1 medicines in the past, or
- when their healthcare provider determines that they meet certain requirements.
HIV-1 is the virus that causes Acquired Immune Deficiency Syndrome (AIDS).
Notes to editors
Cobicistat, emtricitabine and tenofovir alafenamide are from Gilead Sciences, Inc. On December 23, 2014, Janssen and Gilead Sciences, Inc. amended a licensing agreement for the development and commercialization of a once-daily single-tablet regimen combination of darunavir and Gilead’s TAF, emtricitabine and cobicistat. Under the terms of the agreement, Janssen and its affiliates are responsible for the manufacturing, registration, distribution and commercialization of this single-tablet regimen worldwide.
About Janssen
At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease. Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promising science. We are Janssen. We collaborate with the world for the health of everyone in it. Janssen Scientific Affairs, LLC is a part of the Janssen Pharmaceutical Companies of Johnson & Johnson. Learn more at www.janssen.com and follow us at @JanssenGlobal.
*Dr. Eron is a paid consultant for Janssen. He was not compensated for any media work.
References
1 Orkin C, Eron JJ, Rockstroh J, et al. Efficacy and safety of the once-daily, darunavir/cobicistat/emtricitabine/tenofovir alafenamide (D/C/F/TAF) single-tablet regimen (STR) in antiretroviral treatment (ART)-naïve, HIV-1-infected adults: AMBER Week 96 results. Presented at HIV Glasgow 2018, Glasgow, October 28-31, 2018; Available at: https://onlinelibrary.wiley.com/doi/full/10.1002/jia2.25187. Last Accessed October 2018.
2 Eron JJ, Orkin C, Gallant J, et al. A week-48 randomized phase-3 trial of darunavir/cobicistat/emtricitabine/tenofovir alafenamide in treatment-naïve HIV-1 patients. AIDS. 2018;32:1431-1442.
3 Gallant J, Orkin C, Molina JM, et al. Week 48 results of AMBER: a phase 3, randomised, double-blind trial in antiretroviral treatment (ART)-naïve HIV-1-infected adults to evaluate the efficacy and safety of the once-daily, single-tablet regimen (STR) of darunavir/cobicistat/ emtricitabine/tenofovir alafenamide (D/C/F/TAF) versus darunavir/cobicistat (DRV/c) plus emtricitabine/tenofovir disoproxil fumarate (FTC/TDF). Presented at the European AIDS Clinical Society Conference 2017, Milan, October 25-27, 2017; abstract PS8/2. Available at: http://www.abstractserver.com/eacsabstractarchive/. Last accessed October 2018.
4 Panel on Antiretroviral Guidelines for Adults and Adolescents. Guidelines for the Use of Antiretroviral Agents in Adults and Adolescents Living with HIV. Department of Health and Human Services. Available at http://www.aidsinfo.nih.gov/ContentFiles/AdultandAdolescentGL.pdf. Last accessed October 2018.
5 Saag MS, Benson CA, Gandhi RT, et al.Antiretroviral drugs for treatment and prevention of HIV infection in adults: 2018 recommendations of the International Antiviral Society-USA panel. JAMA. 2018;320:379-396.
6 Orkin C, Molina JM, Negredo E, et al. Efficacy and safety of switching from boosted protease inhibitors plus emtricitabine/tenofovir disoproxil fumarate regimens to single-tablet darunavir, cobicistat, emtricitabine, and tenofovir alafenamide at 48 weeks in adults with virologically suppressed HIV-1 (EMERALD): a phase 3, randomised, non-inferiority trial. Lancet HIV. 2018; (1):e23-e34.5.
7 Eron J, Orkin C, Cunningham D, et al. Efficacy and safety of switching from boosted-protease inhibitors (bPI) plus emtricitabine/tenofovir disoproxil fumarate (F/TDF) regimens to the once daily (QD), single-tablet regimen (STR) of darunavir/cobicistat/emtricitabine/tenofovir alafenamide (D/C/F/TAF) in virologically-suppressed, HIV-1-infected adults: week 96 results of the phase 3, randomized, non-inferiority EMERALD trial. Presented at IDWeek 2018, San Francisco, CA, USA, October 3-7, 2018; abstract 1768. Available at: https://idsa.confex.com/idsa/2018/webprogram/Paper72755.html. Last accessed October 2018.
SOURCE: Janssen
Post Views: 194
New Phase 3 AMBER study data continues to demonstrate high rates of virologic suppression at 96 weeks in ART-naïve adults with HIV-1 when treated with SYMTUZA®[1]
GLASGOW, UK I October 30, 2018 I The Janssen Pharmaceutical Companies of Johnson & Johnson unveiled new 96-week data for SYMTUZA® (darunavir 800 mg, cobicistat 150 mg, emtricitabine 200 mg and tenofovir alafenamide 10 mg; (D/C/F/TAF)), a once-daily single-tablet regimen (STR) for the treatment of human immunodeficiency virus type 1 (HIV-1) infection in treatment-naïve and certain virologically suppressed adults, at HIV Glasgow in Scotland.
These 96-week data, which follow on from the earlier 48-week results, reinforce the long-term safety, efficacy and tolerability profile of SYMTUZA® as a treatment for antiretroviral treatment (ART)-naïve adults with HIV-1.1,2 Results demonstrated that a high proportion of ART-naïve adults with HIV-1 (85%, 308/362) achieved virologic suppression (viral load <50 c/mL; FDA-snapshot) at 96 weeks when treated with SYMTUZA®. There was a low virologic failure rate (6%, 20/362; viral load of ≥50 c/mL; FDA-snapshot) in patients treated with SYMTUZA® and no darunavir, primary protease inhibitor or tenofovir resistance-associated mutations emerged in any patient. As previously reported, only 1 patient receiving SYMTUZA® developed a nucleoside reverse transcriptase inhibitor resistance-associated mutation (M184I/V) through week 48. In the current analysis through 96 weeks, only 1 additional patient receiving SYMTUZA® developed a nucleoside reverse transcriptase inhibitor resistance-associated mutation to emtricitabine (M184V).1
Efficacy and safety results were consistent with the 48-week results in the SYMTUZA® group presented at the 2017 European AIDS Clinical Society (EACS) Conference and published in the journal AIDS.1,2,3 SYMTUZA® was well-tolerated with 3% (10/362) of people experiencing adverse event (AE)-related discontinuations over 96 weeks and 3% (11/362) of people experiencing a grade 3 or 4 study drug-related AE. The most common study drug-related AEs (all grades, ≥5% of adults) in the extension period were diarrhea, rash and nausea. Bone, renal and lipid safety results were consistent with known tenofovir alafenamide and cobicistat profiles.1
“The 96-week AMBER data further demonstrate the importance of SYMTUZA® as a treatment option for adults new to HIV therapy who may benefit from a single-tablet regimen that offers the protective barrier to resistance of darunavir along with the tolerability profile of TAF,” said Joseph Eron, M.D., Professor of Medicine and Director, Clinical Core, University of North Carolina Center for AIDS Research, Chapel Hill, NC.* “Based on the DHHS guidelines, darunavir-based regimens are a recommended option in situations where clinicians may not have all genotypic resistance test results, when patients may be at risk for sub-optimal adherence or in rapid initiation scenarios.”
The U.S. Department of Health and Human Services (DHHS) guidelines recommend darunavir for patients who may have suboptimal adherence and face the risk of developing HIV drug resistance, which is when a medication stops working to fight the virus, or for those who may require the rapid initiation of ART before full blood work is available.4 The International Antiviral Society (IAS)-USA guidelines also recommend darunavir-based regimens in rapid initiation scenarios.5
“Long-term AMBER results further build on the growing clinical data set that provides additional support for SYMTUZA® as a treatment option for patients who are starting therapy,” said Richard Nettles, M.D., Vice President, Medical Affairs, Janssen Therapeutics, Janssen Scientific Affairs, LLC. “At Janssen, we are building on our 25-year heritage in HIV and remain committed to the research and development of transformational medicines and solutions that span the continuum of HIV care to address real-world clinical challenges, combat HIV drug resistance and meet the diverse needs of those living with HIV.”
SYMTUZA® was approved by the U.S. Food & Drug Administration (FDA) in July 2018 for treatment-naïve and certain virologically suppressed adults. The approval was based on the results from the two pivotal Phase 3 studies, EMERALD and AMBER.2,3,6 96-week results from the Phase 3 EMERALD trial were recently presented at IDWeek 2018, in San Francisco, CA.7
SYMTUZA® has also been approved by the European Commission (EC) and Health Canada for the treatment of HIV-1 infection in adults and adolescents 12 years of age and older with body weight of at least 40 kg. European approval allows Janssen to market SYMTUZA® in all member states of the European Union and the European Economic Area. Janssen plans additional regulatory filings in other markets worldwide.
SYMTUZA® does not cure or prevent HIV-1 or AIDS.
Please see Important Safety Information below, including Boxed Warning for SYMTUZA®.
To learn more about Janssen’s commitment to the prevention and treatment of HIV, please visit jnj.com/HIV.
About the AMBER clinical trial1,2,3
AMBER is a Phase 3 randomized, double-blind, active-controlled, international, multi-center, non-inferiority study designed to assess the safety and efficacy of SYMTUZA® versus the control in HIV-1 treatment-naïve patients. The control was comprised of two separate medications – darunavir/cobicistat plus emtricitabine/tenofovir disoproxil fumarate – and patients were randomly assigned (362 SYMTUZA®; 363 control). The primary endpoint was non-inferiority of the single-tablet regimen versus the control regarding the proportion of patients that achieved viral suppression at Week 48 (viral load of less than 50 c/mL per FDA-snapshot analysis). Reaching suppression of viral load (or the amount of HIV virus in the blood) is a key treatment goal for people living with HIV. Based on the results of the primary analysis, patients were eligible to receive treatment with SYMTUZA® during an open-label single-group treatment phase up to Week 96.
48-week data have been previously reported.2,3 At Week 96, a high proportion of patients in the SYMTUZA® arm (85%, 308/362) achieved virologic suppression. Viral load of ≥50 c/mL per the FDA snapshot at Week 96 occurred in 20/362 (6%) patients in the SYMTUZA® arm. No darunavir, primary protease inhibitor, or tenofovir resistance-associated mutations emerged in any patient. Through 96 weeks, only two patients receiving SYMTUZA® developed a nucleoside reverse transcriptase inhibitor resistance-associated mutation to emtricitabine (M184I/V).1 SYMTUZA® was well-tolerated with few serious adverse events (n=39, 11%) or adverse event-related discontinuations (n=10, 3%), and no deaths occurred. Bone, renal and lipid safety were consistent with known tenofovir and cobicistat profiles, with a small change in TC/HDL-C ratio.1 Efficacy and safety results in the SYMTUZA® arm were consistent with the 48-week results.1
WHAT IS SYMTUZA®?
SYMTUZA® is a prescription medicine that is used without other antiretroviral medicines to treat Human Immunodeficiency Virus-1 (HIV-1) infection in adults who:
- have not received anti-HIV-1 medicines in the past, or
- when their healthcare provider determines that they meet certain requirements.
HIV-1 is the virus that causes Acquired Immune Deficiency Syndrome (AIDS).
Notes to editors
Cobicistat, emtricitabine and tenofovir alafenamide are from Gilead Sciences, Inc. On December 23, 2014, Janssen and Gilead Sciences, Inc. amended a licensing agreement for the development and commercialization of a once-daily single-tablet regimen combination of darunavir and Gilead’s TAF, emtricitabine and cobicistat. Under the terms of the agreement, Janssen and its affiliates are responsible for the manufacturing, registration, distribution and commercialization of this single-tablet regimen worldwide.
About Janssen
At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease. Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promising science. We are Janssen. We collaborate with the world for the health of everyone in it. Janssen Scientific Affairs, LLC is a part of the Janssen Pharmaceutical Companies of Johnson & Johnson. Learn more at www.janssen.com and follow us at @JanssenGlobal.
*Dr. Eron is a paid consultant for Janssen. He was not compensated for any media work.
References
1 Orkin C, Eron JJ, Rockstroh J, et al. Efficacy and safety of the once-daily, darunavir/cobicistat/emtricitabine/tenofovir alafenamide (D/C/F/TAF) single-tablet regimen (STR) in antiretroviral treatment (ART)-naïve, HIV-1-infected adults: AMBER Week 96 results. Presented at HIV Glasgow 2018, Glasgow, October 28-31, 2018; Available at: https://onlinelibrary.wiley.com/doi/full/10.1002/jia2.25187. Last Accessed October 2018.
2 Eron JJ, Orkin C, Gallant J, et al. A week-48 randomized phase-3 trial of darunavir/cobicistat/emtricitabine/tenofovir alafenamide in treatment-naïve HIV-1 patients. AIDS. 2018;32:1431-1442.
3 Gallant J, Orkin C, Molina JM, et al. Week 48 results of AMBER: a phase 3, randomised, double-blind trial in antiretroviral treatment (ART)-naïve HIV-1-infected adults to evaluate the efficacy and safety of the once-daily, single-tablet regimen (STR) of darunavir/cobicistat/ emtricitabine/tenofovir alafenamide (D/C/F/TAF) versus darunavir/cobicistat (DRV/c) plus emtricitabine/tenofovir disoproxil fumarate (FTC/TDF). Presented at the European AIDS Clinical Society Conference 2017, Milan, October 25-27, 2017; abstract PS8/2. Available at: http://www.abstractserver.com/eacsabstractarchive/. Last accessed October 2018.
4 Panel on Antiretroviral Guidelines for Adults and Adolescents. Guidelines for the Use of Antiretroviral Agents in Adults and Adolescents Living with HIV. Department of Health and Human Services. Available at http://www.aidsinfo.nih.gov/ContentFiles/AdultandAdolescentGL.pdf. Last accessed October 2018.
5 Saag MS, Benson CA, Gandhi RT, et al.Antiretroviral drugs for treatment and prevention of HIV infection in adults: 2018 recommendations of the International Antiviral Society-USA panel. JAMA. 2018;320:379-396.
6 Orkin C, Molina JM, Negredo E, et al. Efficacy and safety of switching from boosted protease inhibitors plus emtricitabine/tenofovir disoproxil fumarate regimens to single-tablet darunavir, cobicistat, emtricitabine, and tenofovir alafenamide at 48 weeks in adults with virologically suppressed HIV-1 (EMERALD): a phase 3, randomised, non-inferiority trial. Lancet HIV. 2018; (1):e23-e34.5.
7 Eron J, Orkin C, Cunningham D, et al. Efficacy and safety of switching from boosted-protease inhibitors (bPI) plus emtricitabine/tenofovir disoproxil fumarate (F/TDF) regimens to the once daily (QD), single-tablet regimen (STR) of darunavir/cobicistat/emtricitabine/tenofovir alafenamide (D/C/F/TAF) in virologically-suppressed, HIV-1-infected adults: week 96 results of the phase 3, randomized, non-inferiority EMERALD trial. Presented at IDWeek 2018, San Francisco, CA, USA, October 3-7, 2018; abstract 1768. Available at: https://idsa.confex.com/idsa/2018/webprogram/Paper72755.html. Last accessed October 2018.
SOURCE: Janssen
Post Views: 194
