The most common moderate/severe related adverse events in the
once-daily and twice-daily groups respectively were: diarrhea (17 percent
versus 15 percent), nausea (seven percent versus five percent), vomiting
(three percent versus four percent), and increased triglycerides (two
percent in both groups). There was no statistical difference between the
groups.
-- At week 48, the overall impact of Kaletra, dosed once-daily or
twice-daily, on grade 3-4 lab abnormalities, including cholesterol and
triglycerides, the liver enzymes, SGOT/AST, and creatinine clearance was
similar.
-- At week 48, there was a statistically significant difference in the
increase of total cholesterol between the once-daily and twice-daily group.
About Abbott's Commitment to Fighting HIV/AIDS
HIV/AIDS is a global problem that demands shared commitment and shared
responsibility. Abbott is committed to working with governments,
multilateral organizations, nongovernmental organizations and patient
groups to expand access to HIV treatments around the world. Abbott has also
made significant investments in expanding manufacturing capacity to meet
the growing demand for HIV treatment in developing countries.
Abbott's lopinavir/ritonavir formulations are among the lowest-priced
protease inhibitors in the developing world. Abbott has been providing its
HIV medicines at a price of US$500 per adult patient per year in all
African and least developed countries since 2002, making these medicines
more affordable than any generic copies.
Abbott and the company's philanthropic foundation, Abbott Fund, have
invested more than US$100 million in the fight against HIV/AIDS in Africa
and the developing world. Abbott Fund-supported programs have served more
than 700,000 children and families. In addition, more than 250,000 patients
have been tested through Abbott Fund-supported voluntary counseling and
testing programs, with thousands being referred to treatment programs.
Abb
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Page: 1 2 3 4 5 6 7 8 Related medicine technology :1.
New Phase 3 Study in Treatment-Naive Adults with HIV Evaluates Efficacy and Safety of Once-Daily PREZISTA(TM)/ritonavir vs. KALETRA(R) as Part of HIV Combination Therapy2.
Ranbaxy Receives Approval to Manufacture and Market Hydrocodone Bitartrate and Acetaminophen Tablets USP3.
Tablet PC Technology Helps Doctors and Patients Focus on Chemotherapy Side Effects, According to Thomson Healthcare Study4.
Health Canada Approves ATRIPLA(R) (efavirenz 600 mg/emtricitabine 200 mg/ tenofovir disoproxil fumarate 300 mg), the First Once-Daily Single Tablet Regimen for HIV5.
New Data Show Improvements in Work Performance in Patients with Chronic Insomnia Treated with AMBIEN CR(R) (zolpidem tartrate extended-release) Tablets CIV6.
A Phase II, Randomized, Double Blind, Placebo-Controlled Dose-Escalating Study, Meets the Clinical Endpoints of MTR106 Tablets During the Treatment of Acute Migraine Attacks Without Aura in Females7.
UCB Announces Positive Phase III Trial Results for Keppra XR(TM) (levetiracetam) Extended-Release Tablets8.
European Commission Approves ATRIPLA(R) (efavirenz 600 mg/emtricitabine 200 mg/tenofovir disoproxil fumarate 300 mg), the First Once-Daily Single Tablet Regimen for Virologically Suppressed Adults With HIV-1 Infection9.
Keppra XR(TM) Extended-Release Tablets Filed with the FDA10.
Lotus Pharmaceuticals, Inc. Achieves Significant Milestones in the Development of Isosorbide Mononitrate Sustained Release Tablets11.
Treximet(TM) (Sumatriptan and Naproxen Sodium) Tablets Approved by FDA for Acute Treatment of Migraine