Healthcare Industry News: raltegravir
News Release - August 5, 2008
ISENTRESS(R) (raltegravir), Merck's First in Class Integrase Inhibitor, Reduced HIV Viral Load and Increased CD4 Cell Counts Through 96 Weeks in Treatment-Naive HIV-Infected Patients When Taken With Other Anti-HIV MedicinesEfficacy and Tolerability Profile Consistent With Data Seen in Approved Treatment-Experienced Indication
WHITEHOUSE STATION, N.J.--(HSMN NewsFeed)--ISENTRESS® (raltegravir), Merck & Co., Inc.’s first-in-class integrase inhibitor, in combination with two other anti-HIV medicines, reduced HIV viral load to undetectable levels (less than 50 copies/mL) in 83 percent of previously untreated (treatment-naïve) HIV-infected patients which was comparable to that seen with efavirenz (Sustiva®/STOCRIN®)*, which reduced HIV viral load to undetectable levels in 84 percent of treatment-naïve HIV-infected patients when also combined with the same anti-HIV medicines in patients through 96 weeks of treatment. Patients taking ISENTRESS experienced a mean increase in CD4 cell counts of 221 cells/mm3 without adverse impact on total or low-density lipoprotein (LDL) cholesterol, or triglycerides (exploratory endpoints). Results from this ongoing Phase II study were presented today at the 17th International AIDS Conference (AIDS 2008) in Mexico City, Mexico.
“These findings are consistent with the efficacy and safety data seen with ISENTRESS in treatment-experienced patients,” said Martin Markowitz, M.D., study investigator and clinical director of the Aaron Diamond AIDS Research Center in New York. “Viral load reductions were sustained through 96 weeks in this study, the longest conducted to date with ISENTRESS."
ISENTRESS studied in nearly 200 previously untreated patients
These findings are from an ongoing multi-center, dose-ranging, double-blind, randomized trial of previously untreated HIV-infected patients. In this study, 198 treatment-naïve, HIV-infected patients received either ISENTRESS administered orally twice daily in combination with tenofovir (Viread® ) and lamivudine (Epivir®) or 600 mg efavirenz dosed orally once daily in combination with the same agents. During the first 48 weeks of the study, four dose regimens of ISENTRESS (100, 200, 400 and 600 mg twice daily) were studied. After 48 weeks, all ISENTRESS groups received 400 mg dosed twice daily. The primary endpoints were reductions in HIV RNA less than 400 copies/mL and the evaluation of safety at 96 weeks. The evaluation of total cholesterol, LDL cholesterol and triglycerides were exploratory endpoints.
Reduction in viral load and increase in CD4 cell counts maintained through 96 weeks of treatment with ISENTRESS
At baseline, geometric mean HIV RNA for patients on the combined regimen including ISENTRESS was approximately 55,000 copies/mL (n=160) and for the efavirenz regimen was approximately 68,000 copies/mL (n=38). Mean baseline CD4 cell counts were 305 and 280 cells/mm3 for the groups receiving ISENTRESS and efavirenz, respectively.
After 96 weeks of therapy, 83 percent of patients receiving the regimen with ISENTRESS achieved reductions in HIV RNA levels below 50 copies/mL. Results were comparable for patients taking the regimen containing efavirenz, with 84 percent of patients achieving reductions in HIV RNA levels below 50 copies/mL in the same time period. Similarly, 84 percent of patients receiving the regimen containing ISENTRESS maintained reductions in HIV RNA levels to below 400 copies/mL compared to 84 percent of patients taking the regimen containing efavirenz. Patients on both treatment regimens experienced increases in CD4 cell counts. At 96 weeks of treatment, the mean increase from baseline in CD4 cell count was 221 cells/mm3 for patients taking ISENTRESS and 232 cells/mm3 for patients taking efavirenz.
Tolerability profile and effect on lipid levels
The most commonly reported adverse experiences in patients receiving ISENTRESS and efavirenz, respectively, were diarrhea (6.9 percent versus 10.5 percent), nausea (12.5 versus 13.2 percent), dizziness (8.8 versus 28.9 percent), headache (8.8 percent versus 23.7 percent), abnormal dreams (6.3 percent versus 18.4 percent), insomnia (8.1 percent versus 10.5 percent) and nightmares (0 percent versus 10.5 percent). Neuropsychiatric adverse events, which included abnormal dreams, depression, nightmare and suicidal thoughts, were reported less frequently with the ISENTRESS group compared to the efavirenz group, occurring respectively in 16 versus 32 percent of patients through Week 96; most of these had occurred earlier in the study by Week 48.
ISENTRESS had neutral effect on total and LDL cholesterol, or triglycerides. The mean changes from baseline at Week 96 for ISENTRESS and efavirenz, respectively, were +1.1 mg/dL and +24.0 mg/dL (p=0.002) for total cholesterol; -5.8 mg/dL and +4.4 mg/dL (p=0.045) for LDL cholesterol; +7.4 mg/dL and +13.0 mg/dL (p=0.017) for HDL cholesterol; -10.8 mg/dL and +13.4 mg/dL (p=0.145) for triglycerides; and -0.7 mg/dL and -0.7 mg/dL (P=0.689) for total: HDL ratio.
Important safety information about ISENTRESS
ISENTRESS does not cure HIV or AIDS and does not prevent passing HIV to others. Healthcare providers should know that immune reconstitution syndrome has been reported in patients treated with antiretroviral therapy, which may necessitate further evaluation and treatment.
In the clinical trials involving treatment-experienced patients, the most commonly reported adverse experiences of any severity (mild, moderate or severe) for ISENTRESS plus optimized background therapy (OBT) versus placebo plus OBT, respectively, regardless of drug relationship were diarrhea (16.6 percent vs. 19.5 percent), nausea (9.9 percent vs. 14.2 percent), headache (9.7 percent vs. 11.7 percent) and fever (4.9 percent vs. 10.3 percent).
Creatine kinase elevations were observed in subjects who received ISENTRESS. Myopathy and rhabdomyolysis have been reported; however, the relationship of ISENTRESS to these events is not known. ISENTRESS should be used with caution in patients at increased risk of myopathy or rhabdomyolysis, such as patients receiving concomitant medication known to cause these conditions.
Results from pooled safety analyses from three separate studies (BENCHMRK-1, BENCHMRK-2 and a Phase II dose ranging study) in treatment-experienced patients taking 400 mg of ISENTRESS dosed twice daily plus OBT or placebo plus OBT showed that after 24 weeks of therapy the rates of discontinuation of therapy due to adverse experiences were 2.0 percent in patients receiving ISENTRESS plus OBT and 1.4 percent in patients receiving placebo plus OBT. In addition, drug-related clinical adverse events of moderate to severe intensity occurring in greater than or equal to 2.0 percent of patients were diarrhea (3.7 percent vs. 4.6 percent), nausea (2.2 percent vs. 3.2 percent) and headache (2.4 percent vs. 1.4 percent) for ISENTRESS plus OBT and placebo plus OBT, respectively.
Based on the results of drug interaction studies and the clinical trials data, no dose adjustment of ISENTRESS is required when coadministered with other antiretroviral agents. Also, preclinical studies show that ISENTRESS is not metabolized by cytochrome P450 enzymes. Caution should be used when coadministering ISENTRESS with strong inducers of uridine diphosphate glucuronosyltransferase (UGT) 1A1 (e.g., rifampin) due to reduced plasma concentrations of ISENTRESS.
ISENTRESS is the first medicine to be approved in a new class of antiretroviral drugs called integrase inhibitors. ISENTRESS works by inhibiting the insertion of HIV-1 DNA into human DNA by the integrase enzyme. Inhibiting integrase from performing this essential function limits the ability of the virus to replicate and infect new cells. There are drugs in use that inhibit two other enzymes critical to the HIV-1 replication process – protease and reverse transcriptase – but ISENTRESS is the only drug approved that inhibits the integrase enzyme.
In October 2007, the U.S. Food and Drug Administration granted ISENTRESS accelerated approval for use in combination with other antiretroviral agents for the treatment of HIV-1 infection in treatment-experienced adult patients with evidence of viral replication with HIV-1 strains resistant to multiple antiretroviral agents. ISENTRESS is a single 400 mg tablet taken twice daily without regard to food. ISENTRESS does not require boosting with ritonavir.
Merck HIV Research
Merck is committed to developing innovative therapies that offer advances in the treatment of infectious diseases – including HIV. Merck's efforts to develop investigational treatments for HIV and AIDS have been under way for more than 20 years and continue today. Merck began its HIV integrase inhibitor research in 1993 and was the first to demonstrate inhibition of HIV integrase in vitro and in vivo.
Prevalence of HIV and AIDS
In 2006, more than one million Americans were living with HIV and AIDS, and it is estimated that approximately more than 56,000 new cases of HIV and AIDS are diagnosed each year in the United States.
Worldwide, an estimated 33 million people are infected with HIV and AIDS, and more than two million new infections occurred in 2007.
Merck's commitment to providing access to treatment
Merck is committed to ensuring access to our antiretroviral medicines (ARVs) through a differential pricing policy that provides our ARVs at dramatically lower prices-at which Merck does not profit-to people living in the world's least developed countries and those hardest hit by the pandemic, as defined by various United Nations indices.
Also, Merck is committed to seeking additional ways to reduce the cost of its ARVs for people living in the world's poorest countries and those hardest hit by the pandemic, including through partnering with external manufacturers and suppliers to achieve incremental efficiencies and cost savings.
In the United States, Merck is freezing the price for AIDS Drug Assistance Programs (ADAP) of ISENTRESS at its launch price until December 31, 2010. ADAP is a unique fixed-funding program with a flat federal budget whose cost burden and patient load continues to grow. In freezing the price of ISENTRESS, Merck will help mitigate the funding challenges of these programs.
Since 2006, when Merck established a worldwide expanded access program with ISENTRESS for HIV patients with limited or no treatment options, more than 9,000 patients have enrolled in early access programs for ISENTRESS globally.
Merck & Co., Inc. is a global research-driven pharmaceutical company dedicated to putting patients first. Established in 1891, Merck currently discovers, develops, manufactures and markets vaccines and medicines to address unmet medical needs. The Company devotes extensive efforts to increase access to medicines through far-reaching programs that not only donate Merck medicines but help deliver them to the people who need them. Merck also publishes unbiased health information as a not-for-profit service. For more information, visit www.merck.com.
This press release contains "forward-looking statements" as that term is defined in the Private Securities Litigation Reform Act of 1995. These statements are based on management's current expectations and involve risks and uncertainties, which may cause results to differ materially from those set forth in the statements. The forward-looking statements may include statements regarding product development, product potential or financial performance. No forward-looking statement can be guaranteed and actual results may differ materially from those projected. Merck undertakes no obligation to publicly update any forward-looking statement, whether as a result of new information, future events, or otherwise. Forward-looking statements in this press release should be evaluated together with the many uncertainties that affect Merck's business, particularly those mentioned in the risk factors and cautionary statements in Item 1A of Merck's Form 10-K for the year ended Dec. 31, 2007, and in any risk factors or cautionary statements contained in the Company's periodic reports on Form 10-Q or current reports on Form 8-K, which the Company incorporates by reference.
ISENTRESS® is a registered trademark of Merck & Co., Inc. Whitehouse Station, NJ USA.
* Bristol-Myers Squibb has exclusive marketing rights to efavirenz in the United States (including territories and possessions), Canada, United Kingdom, Republic of Ireland, France (continental only), Spain, Italy and Germany, and markets efavirenz under its trademark Sustiva®. Through its subsidiaries and marketing partners, Merck has exclusive marketing rights in all other countries worldwide, and markets efavirenz under the trademark STOCRIN®. All other brands are trademarks of their respective owners and are not trademarks of Merck & Co., Inc.
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