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Acorda Therapeutics Stock News
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At Close: Apr 26, 2024
India's drug regulator grants Gilead Sciences marketing authorization for remdesivir
04:02pm, Tuesday, 02'nd Jun 2020
Read more about India's drug regulator grants Gilead Sciences marketing authorization for remdesivir on Devdiscourse
COVID-19: India’s drug regulator grants Gilead Sciences marketing authorisation for remdesivir
01:19pm, Tuesday, 02'nd Jun 2020
An earlier study results showed that when treating patients with severe disease - those who require non-invasive supplemental oxygen - 5 days of remdesivir led to similar improvements as a 10-day cour
Novacyt shares drop as France refuses to refund virus test
10:52am, Tuesday, 02'nd Jun 2020
Read more about Novacyt shares drop as France refuses to refund virus test on Devdiscourse
India's drug regulator grants Gilead Sciences marketing authorisation for remdesivir
06:59am, Tuesday, 02'nd Jun 2020
Read more about India's drug regulator grants Gilead Sciences marketing authorisation for remdesivir on Devdiscourse
Strides Pharma gets USFDA nod for generic ointment to treat skin conditions
06:43am, Tuesday, 02'nd Jun 2020
Read more about Strides Pharma gets USFDA nod for generic ointment to treat skin conditions on Devdiscourse
India's drug regulator grants Gilead Sciences marketing authorisation for remdesivir
03:23am, Tuesday, 02'nd Jun 2020
India's drug regulator has granted US pharma giant Gilead Sciences marketing authorisation for its anti-viral drug remdesivir for "restricted emergency use" on hospitalised COVID-19 patients.
Sensex, Nifty close nearly 2% higher, shrug Moody’s downgrade
03:11am, Tuesday, 02'nd Jun 2020
Sensex advanced 522 points or 1.6% to close at 33,825. Nifty climbed 153 points or 1.6% to end at 9,979.Bajaj Finance, Kotak Bank and IndusInd Bank, surging 6-8% were top Sensex gainers
India's drug regulator grants Gilead Sciences marketing authorisation for remdesivir
01:54am, Tuesday, 02'nd Jun 2020
India's drug regulator has granted US pharma giant Gilead Sciences marketing authorisation for its anti-viral drug remdesivir for 'restricted emergency use' on hospitalised COVID-19 patients in view o
India's drug regulator grants Gilead Sciences marketing authorization for remdesivir
07:27pm, Monday, 01'st Jun 2020
Read more about India's drug regulator grants Gilead Sciences marketing authorization for remdesivir on Devdiscourse
FDA Issues Emergency Use Authorization for Impella RP as Therapy for COVID-19 Patients with Right Heart Failure
12:00am, Monday, 01'st Jun 2020
The United States Food and Drug Administration (FDA) has issued an emergency use authorization (EUA) for Impella RP to include patients suffering from
Hikma Pharmaceuticals : USA launches Dicyclomine Hydrochloride Oral Solution USP in US | MarketScreener
12:12pm, Friday, 29'th May 2020INSIDE STORY: How Kogi is turning a blind eye to patients with COVID-19 symptoms - TheCable
09:11am, Thursday, 28'th May 2020
It was scorching hot on Saturday afternoon in Lokoja, Kogi, when Godwin (not real name) managed to drag himself to one of the hospitals in th
Biocon gets DCGI nod for device to treat critical COVID-19 patients
11:22am, Wednesday, 27'th May 2020
The company has been granted licence for emergency use of CytoSorb, an extracorporeal blood purification device CytoSorb to reduce pro-inflammatory cytokines levels, to treat COVID-19 patients who are
Aurinia Pharmaceuticals Inc. (Nasdaq:AUPH / TSX:AUP) (“Aurinia” or the “Company”), a late-stage clinical biopharmaceutical company focused on advancin
Germany Respiratory Devices Market 2019-2025 - ResearchAndMarkets.com
12:00am, Monday, 25'th May 2020
The