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FDA

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  • FDA
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‘First probable case of Monkeypox in West Virginia’ -WTRF.com Report

By Benzinga Newsdesk
July 8, 11:02 AM
https://www.wtrf.com/west-virginia/first-probable-case-of-monkeypox-in-west-virginia/?utm_medium=referral&utm_campaign=socialflow&utm_source=t.co

AEMD

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  • FDA
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‘First cases of monkeypox confirmed in South Carolina’ -News19 Report

By Benzinga Newsdesk
July 8, 9:27 AM
https://www.wltx.com/article/news/health/confirmed-first-cases-of-monkeypox-in-south-carolina-midlands-lowcountry-dhec/101-710eb9a5-4f1c-44d0-9b35-0a59923a70f7

AEMD

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  • Biotech
  • FDA
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Horizon Therapeutics Receives FDA Approval For Uncontrolled Gout Candidate

By Ragothaman Srinivasan
July 8, 9:03 AM
The U.S. Food and Drug Administration (FDA) has approved Horizon Therapeutics’ (NASDAQ: HZNP) supplemental Biologics License Application (sBLA) for expanding the labeling to include KRYSTEXXA (pegloticase) injection co-administered with methotrexate, in patients with uncontrolled gout.

HZNP

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The Daily Biotech Pulse: Pfizer Inks Pact With Africa For COVID-19 Pills, Emergent Bio & Ridgeback To Increase Access To Ebola Treatment, ADC Therapeutics & Sobi In European Pact For Lymphoma Drug

By Vandana Singh
July 8, 8:19 AM
Here's a roundup of top developments in the biotech space over the last 24 hours:

ADCT

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  • FDA
  • News

Novavax Files In Switzerland For Expanded Conditional Marketing Authorization Of Nuvaxovid For Adolescents Aged 12-17, Booster In Individuals Aged 18 & Over

By Benzinga Newsdesk
July 7, 5:48 PM
-Reuters

NVAX

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  • Biotech
  • FDA
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Inventiva Announces The Screening Of The First Patient In LEGEND, A Phase IIa Combination Trial With Lanifibranor And Empagliflozin In Patients With NASH And T2D

By Benzinga Newsdesk
July 7, 4:01 PM
The Phase IIa Proof-of-Concept study is designed to assess the safety and efficacy of lanifibranor in combination with the SGLT2 inhibitor empagliflozin for the treatment of patients with non-cirrhotic non-alcoholic

IVA

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  • FDA
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‘Louisiana confirms first case of monkeypox’ -Nola.com

By Benzinga Newsdesk
July 7, 1:10 PM
https://www.nola.com/news/healthcare_hospitals/article_42100524-fbf9-11ec-bd50-1719af89cf9b.html

AEMD

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1 minute read
  • FDA
  • News

Six Countries Seek Expansion Of Partial IP Waiver For Covid-19 Vaccines To Drugs And Tests By Year-End

By Benzinga Newsdesk
July 7, 10:38 AM
-Reuters

AZN

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The Daily Biotech Pulse: Merck’s Seagen Buyout Advances, Adverum Restructures, Pharmacists Get OK To Prescribe Pfizer COVID-19 Pill

By Vandana Singh
July 7, 10:03 AM
Here's a roundup of top developments in the biotech space over the last 24 hours:

ADVM

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1 minute read
  • FDA
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Public Health Authority Slovakia Confirms First Case Of Monkeypox

By Benzinga Newsdesk
July 7, 9:56 AM
-Reuters

AEMD

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