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Hikma Pharma Launches KLOXXADO Nasal Spray 8mg

Hikma Pharma Launches KLOXXADO Nasal Spray 8mg
finanznachrichten.de - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from finanznachrichten.de Daily Mail and Mail on Sunday newspapers.

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Emergent BioSolutions Inc (EBS) Q4 2020 Earnings Call Transcript

Emergent BioSolutions Inc (EBS) Q4 2020 Earnings Call Transcript
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DBFD Launches Drug Abuse Response Team (DART)

Feb 15, 2021 1:03 PM
Daytona Beach, FL - A collaborative effort between the Daytona Beach Fire Department (DBFD) Community Paramedicine Program, the Daytona Beach Police Department (DBPD), and the Stewart-Marchman Alliance is already seeing results. The goal of the Drug Abuse Response Team (DART) is to identify drug users and assist in bringing them to recovery programs directly from the field. The team has completed eight field visits while seeing more than 30 individuals during the first weeks of operation. The clients are provided Narcan Nasal Spray that will reverse the effects of an opioid overdose in an emergency. They are also provided with an informational packet that includes resources on substance abuse and contact information for local assistance programs. DART members talk to clients and encourage them to take advantage of the program in order for them to rehabilitate and overcome drug addiction. If you know someone who may benefit from DART or would ....

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Orexo expects FDA filing of OX124 mid 2022

Orexo expects FDA filing of OX124 mid 2022
- OX124 is designed to reverse the effect of the most powerful synthetic opioids
- Synthetic opioids are behind the majority of fatal overdoses in the US, a development expected to increase due to Covid-19
- New Drug Application (NDA) filing expected mid 2022
UPPSALA, Sweden, Jan. 29, 2021 /PRNewswire/ Orexo AB (publ.),
(STO: ORX) (OTCQX: ORXOY) today announces that it is expecting to file its flagship pharmaceutical pipeline asset OX124 with the US Food and Drug Administration mid-2022. OX124 is expected to follow the FDA s standard submission and review timelines, as the FDA did not grant Fast Track Designation to the product. Given the medical need to swiftly make powerful rescue medications available to those in need, Orexo will continue to work closely with the FDA to expedite the route to approval. The FDA s decision is not related to the product, but is based on an overall assessment whether the development p ....

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