Cipla ready to launch low dose HIV drug 'Efavirenz'
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New Delhi, Nov 30: Drug major Cipla Ltd today said it is ready to launch low dose 'Efavirenz' used in treatment of HIV infection.
On the eve of World AIDS day, the company announced "its readiness to supply its combinations Tenofovir/Emtricitabine/ Efavirenz and Tenofovir/Lamivudine/Efavirenz with a dose of 400 mg of Efavirenz as a first-line initial therapy for HIV infection", Cipla said in a BSE filing.
"Studies now support the use of Efavirenz 400 mg as a substitute for Efavirenz 600 mg in cases where there is no co-infection with tuberculosis. Efavirenz 600 mg is currently used in antiretroviral therapy (ART) and is highly effective.
"However, it is known to have significant side effects, which can be very distressing for those taking it for treatment of HIV infection," it added.
Cipla further said: "Studies found that the reduced dose of 400 mg Efavirenz was non-inferior to the standard dose of 600 mg Efavirenz dose when combined with Tenofovir/ Emtricitabine (TDF/FTC) and Tenofovir/ Lamivudine (TDF/ 3TC) as initial HIV therapy. Both doses demonstrated similar safety profiles."
On the eve of World AIDS day, the company announced "its readiness to supply its combinations Tenofovir/Emtricitabine/ Efavirenz and Tenofovir/Lamivudine/Efavirenz with a dose of 400 mg of Efavirenz as a first-line initial therapy for HIV infection", Cipla said in a BSE filing.
"Studies now support the use of Efavirenz 400 mg as a substitute for Efavirenz 600 mg in cases where there is no co-infection with tuberculosis. Efavirenz 600 mg is currently used in antiretroviral therapy (ART) and is highly effective.
"However, it is known to have significant side effects, which can be very distressing for those taking it for treatment of HIV infection," it added.
Cipla further said: "Studies found that the reduced dose of 400 mg Efavirenz was non-inferior to the standard dose of 600 mg Efavirenz dose when combined with Tenofovir/ Emtricitabine (TDF/FTC) and Tenofovir/ Lamivudine (TDF/ 3TC) as initial HIV therapy. Both doses demonstrated similar safety profiles."
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