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Mashup Score: 0
The FDA deemed AstraZeneca’s PT027 to have a favorable risk-benefit profile for treating asthma in patients aged 18 or older but was less keen on supporting the drug in younger populations.
Source: BioSpaceCategories: Healthcare Professionals, Latest HeadlinesTweet
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Mashup Score: 0
San Diego-based Arcturus Therapeutics signed a strategic collaboration and licensing deal with CSL Seqirus to help develop and commercialize vaccines.
Source: BioSpaceCategories: Infectious Disease, Latest HeadlinesTweet
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Mashup Score: 0GSK’s Blenrep for Multiple Myeloma Misses Mark in Phase III Confirmatory Trial | BioSpace - 2 year(s) ago
GSKs Blenrep misses the mark in the Phase III DREAMM-3 trial for relapsed or refractory multiple myeloma (RRMM), possibly putting the drug’s continued approval at risk.
Source: BioSpaceCategories: Hem/Oncs, Latest HeadlinesTweet
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Mashup Score: 4Roche introduces the navify brand for its digital health solutions at HLTH 2022 | BioSpace - 2 year(s) ago
Roche introduces the navify brand for its digital health solutions at HLTH 2022 – read this article along with other careers information, tips and advice on BioSpace
Source: BioSpaceCategories: Healthcare Professionals, Latest HeadlinesTweet
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Mashup Score: 1Roche introduces the navify brand for its digital health solutions at HLTH 2022 | BioSpace - 2 year(s) ago
Roche introduces the navify brand for its digital health solutions at HLTH 2022 – read this article along with other careers information, tips and advice on BioSpace
Source: BioSpaceCategories: Healthcare Professionals, Latest HeadlinesTweet
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Mashup Score: 2
An investigator in the Phase III trial for Biogen and Eisai’s experimental Alzhiemer’s drug, lecanemab, is attributing a patient’s death to the treatment.
Source: BioSpaceCategories: Hem/Oncs, Latest HeadlinesTweet-
@barttels2 @MadhavThambiset @AlbertoEspay @AE_MD @LonSchneiderMD @ProfRobHoward @jasonkarlawish @MemoryDoc @geoperry @samgandy @cureffi @adamfeuerstein @damiangarde @PLutsey @Jasonmmast @EisaiUS @maxonwifi Eisai Responds to Claims Linking Patient Death to Lecanemab https://t.co/Jdh98VKHES via @H_M_MAC
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Mashup Score: 0Gilead's Hopes for HDV Approval Delayed after CRL | BioSpace - 2 year(s) ago
The FDA issued a Complete Response Letter regarding Gilead’s Biologics License Application for bulevirtide, citing concerns regarding the manufacture and delivery of the drug.
Source: BioSpaceCategories: Infectious Disease, Latest HeadlinesTweet
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Mashup Score: 0
An FDA adcomm that met Wednesday to vote on GlaxoSmithKline’s daprodustat for adult patients with anemia due to chronic kidney disease (CKD) produced mixed results.
Source: BioSpaceCategories: Cardiologists, Latest HeadlinesTweet
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Mashup Score: 1
Biogen and others are seeing the value in, particularly, non-prescription digital therapeutics, as complementary companion therapies to disease-modifying drugs.
Source: BioSpaceCategories: Healthcare Professionals, Latest HeadlinesTweet
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Mashup Score: 0Early Human Data Validates Effectiveness of Pfizer-BioNTech Omicron Booster | BioSpace - 2 year(s) ago
Pfizer and BioNTech released early data Thursday morning from a Phase II/III trial assessing an Omicron-specific booster that showed it provided significant protection, confirming early research.
Source: BioSpaceCategories: Infectious Disease, Latest HeadlinesTweet
FDA Adcomm Backs AstraZeneca's Asthma Drug for Adults, but not Children | BioSpace https://t.co/JXUknr9Jnk