Examples of using Sofosbuvir in English and their translations into Malay
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LediHep contains a combination of Ledipasvir and Sofosbuvir.
Sofosbuvir is a drug used for hepatitis C virus(HCV) infection, with a high cure rate.
Generic Harvoni is a combination of ledipasvir and sofosbuvir.
Sofosbuvir and ledipasvir are antiviral medicines that inhibits hepatitis C virus(HCV) from growing in your….
Sofocure I contains a combination of Ledipasvir and Sofosbuvir.
Hepcinat(Sofosbuvir) is an antiviral medication that prevents hepatitis C virus(HCV) from multiplying in your body.
Vosevi is a fixed-dose,combination tablet containing two previously approved drugs- sofosbuvir and velpatasvir- and a new drug, voxilaprevir.
Ledipasvir and sofosbuvir are antiviral medications that prevent the hepatitis C virus(HCV) from multiplying in your body.
Vosevi(FDA approval in July2017), is a fixed-dose, combination tablet containing two previously approved drugs(sofosbuvir and velpatasvir), and a new drug, voxilaprevir.
Ledipasvir and Sofosbuvir are antiviral medications that help to prevent hepatitis C virus(HCV) cells from multiplying in your body.
Sometimes a doctor will prescribe this along with the medication sofosbuvir, where a 12-week course of treatment for both medications totals about $150,000.
DNDi conducted the STORM-C-1 open label trial to assess the efficacy, safety,tolerance and pharmacokinetics of the drug candidate ravidasvir combined with sofosbuvir.
Vosevi is the first treatment approved forpatients who have been previously treated with sofosbuvir or other drugs for HCV that inhibit a protein called NS5A.
DND administrated the STORM-C-1 open-label trial in order to measure the efficacy, safety, tolerance,and pharmacokinetics of the drug ravidasvir in combination with sofosbuvir.
Vosevi is approved for patients who have been treated with sofosbuvir or direct-acting antiviral drugs used for treating hepatitis C virus that inhibit NS5A protein.
In a Phase III clinical trial in Egypt, conducted by Pharco, ravidasvir showed cure rates of up to 100% in patients withgenotype 4 when used in combination with sofosbuvir.
He, however, lauded Putrajaya's efforts in reducing the price of the Sofosbuvir medication for local Hepatitis C patients, where treatment could cost as much as RM500 in public hospitals.
The non-profit research and development organization Drugs for Neglected Diseases initiative(DNDi) has been running clinical trials in Malaysia, in partnership with the Ministry of Health and Egyptian drug manufacturer Pharco Pharmaceuticals,to test a pan-genotypic treatment combining sofosbuvir with the drug candidate ravidasvir.
Chronically infected adults were treated with the ravidasvir/ sofosbuvir combination for 12 weeks for patients without cirrhosis of the liver, and for 24 weeks for those with compensated cirrhosis.
Vosevi is the first treatment approved for patients who have beenpreviously treated with the direct-acting antiviral drug sofosbuvir or other drugs for HCV that inhibit a protein called NS5A.
In the second trial, investigators examined Vosevi versus sofosbuvir and velpatasvir in adults with HCV genotypes 1, 2, or 3 who previously failed treatment with sofosbuvir, but not an NS5A inhibitor drug.
The fixed-dose tablet is the first treatment approved forpatients who have been previously treated with sofosbuvir or other HCV drugs that inhibit nonstructural protein 5A(NS5A).
In September 2017,the government of Malaysia issued a“government-use” licence on sofosbuvir patents to allow 400,000 people living with hepatitis C in Malaysia to access generic HCV regimens in public hospitals.
To ensure scale-up of our hepatitis C treatment programme,the government wishes to purchase generic sofosbuvir at the lowest possible price and make it available in the public health system throughout the country.”.
In September 2017, The Star reported that the Governmentannounced it had issued a"government-use" license on sofosbuvir to allow 400,000 Hepatitis C patients in Malaysia to access generic version of the drug in public hospitals.
The second trial compared 12 weeks of Vosevi with the previously approved drugs sofosbuvir and velpatasvir in adults with genotypes 1, 2 or 3 who had previously failed treatment with sofosbuvir but not an NS5A inhibitor drug.