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Glenmark, Cipla stocks surge after nod to launch drugs for mild-to-moderat
Updated : 6 years, 2 months ago IST
Mumbai (Maharashtra) [India], June 22 (ANI): Glenmark Pharmaceuticals' share price surged 30 per cent on Monday to Rs 531.80 per unit after it became the first pharmaceutical company in India to receive regulatory approval to make and sell oral antiviral drug favipiravir for treating mild-to
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Drug with new approach on impeding DNA repair shows promising results: Stu
Updated : 6 years, 2 months ago IST
Boston [USA], June 21 (ANI): Patients with high-grade serious ovarian cancer (HGSOC) who were treated with the drug, berzosertib, and chemotherapy lived substantially longer before their disease began to worsen than did those treated with chemotherapy alone, according to a recent study.
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Domestic pharma giants-- Cipla, Hetero got DCGI's nod to manufacture, sell
Updated : 6 years, 2 months ago IST
New Delhi [India], June 21 (ANI): In a significant development, India's top drug regulator has given nod to two domestic pharmaceutical companies--Cipla and Hetero for marketing authorization of anti-viral drug Remdesivir only for "restricted emergency use" on COVID-19 patients with moderate
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Anti-viral drug Favipiravir shows clinical improvement in mild, moderate C
Updated : 6 years, 2 months ago IST
New Delhi [India], June 20 (ANI): Domestic pharmaceuticals Glenmark on Saturday informed that their antiviral drug -- Favipiravir -- has shown clinical improvement of up to 88 per cent in mild to moderate COVID-19 cases, including those with co-morbidities.
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Anti-viral drug favipiravir gets DGCI nod for 'restricted emergency use' i
Updated : 6 years, 2 months ago IST
New Delhi [India], June 19 (ANI): The Drug Controller General of India (DCGI) has granted permission to anti-viral drug favipiravir for "restricted emergency use" in mild to moderate cases of COVID-19, a senior government official confirmed to ANI.
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CSIR gets nod for Phase III trial of antiviral drug Umifenovir
Updated : 6 years, 2 months ago IST
New Delhi [India], June 19 (ANI): CSIR constituent lab CSIR-Central Drug Research Institute (CDRI) Lucknow has received permission for carrying out Phase III trial of antiviral drug Umifenovir, Union Health Minister Dr Harsh Vardhan said on Friday.
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US left with 63 million doses of anti-malarial drug after FDA revoked its
Updated : 6 years, 2 months ago IST
Washington D.C. [USA], June 19 (ANI): The US federal government is now left with 63 million doses of hydroxychloroquine sulfate (HCQ) in its stockpile after the Food and Drug Administration (FDA) earlier this week, revoked the permission for use of anti-malarial drug in treating COVID-19
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Cipla expands partnership with Roche Pharma to improve access for oncology
Updated : 6 years, 2 months ago IST
Mumbai (Maharashtra) [India], June 18 (ANI): Pharmaceutical majors Cipla and Roche Products India said on Thursday they have entered into an agreement to provide better access to innovative medicines for patients in India.
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Aarya: Sushmita Sen introduces Sikandar Kher as Daulat
Updated : 6 years, 2 months ago IST
New Delhi [India], June 17 (ANI): Actor Sushmita Sen on Wednesday took to social media and introduced co-actor Sikandar Kher's character - Daulat, who is to be seen alongside Sen in her upcoming debut web series 'Aarya.'
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Dexamethasone drug emerges as a fresh hope in fight against COVID-19
Updated : 6 years, 3 months ago IST
New Delhi [India], June 17 (ANI): United Kingdom's RECOVERY trial has emerged as a new hope in the fight against COVID-19 pandemic with researchers claiming that dexamethasone, the inexpensive and widely available steroid is the first drug that has proven to reduce deaths in COVID-19 patient
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Preliminary study reveals steroid dexamethasone helps treating critical CO
Updated : 6 years, 3 months ago IST
London [UK], June 16 (ANI): Amid the rising number of coronavirus cases globally and the rush to find proper vaccinations for the disease, two researchers in the UK have found steroid drug dexamethasone helpful in treating the critical patients dependent on ventilators or oxygen.
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MedAlliance gains CE Mark approval for coronary SELUTION SLR™ Siroli
Updated : 6 years, 3 months ago IST
Mumbai (Maharashtra) [India] June 16 (ANI/PRNewswire): MedAlliance has announced the award of its second CE Mark: SELUTION SLR™ 014 PTCA, a novel Sirolimus Drug Eluting Balloon (DEB), for the treatment of coronary arterial disease.
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