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Belcher Pharmaceuticals Receives Form 483 for Lab and Production Quality Issues

  • Post author:PacConAdmin
  • Post published:March 22, 2022
  • Post category:Drug Industry Daily

Belcher Pharmaceuticals received a Form 483 from the FDA for several deficiencies observed during a Nov. 1- 15, 2021, inspection of its drug manufacturing facility in Largo, Fla. Source: Drug…

Continue ReadingBelcher Pharmaceuticals Receives Form 483 for Lab and Production Quality Issues

Volastra Teams up With BMS to Develop Targeted Cancer Drugs

  • Post author:PacConAdmin
  • Post published:March 21, 2022
  • Post category:Drug Industry Daily

New York-based drug discovery company Volastra Therapeutics has signed a deal with Bristol Myers Squibb (BMS) potentially worth up to $1.1 billion to create new medicines for undisclosed targets. Source:…

Continue ReadingVolastra Teams up With BMS to Develop Targeted Cancer Drugs

Baxter Gets Form 483 for Observations of Recurring Vermin, Lack of Protocols and Access

  • Post author:PacConAdmin
  • Post published:March 21, 2022
  • Post category:Drug Industry Daily

Baxter Pharmaceuticals Solutions’ contract manufacturing facility in Bloomington, Ind., has received a Form 483 for several deficiencies observed during an FDA inspection from Nov. 2 through Nov. 10, 2021. Source:…

Continue ReadingBaxter Gets Form 483 for Observations of Recurring Vermin, Lack of Protocols and Access

USPTO to Decide on Patent Extension for AAV Tech Used in Novartis’ Zolgensma

  • Post author:PacConAdmin
  • Post published:March 21, 2022
  • Post category:Drug Industry Daily

The FDA won’t weigh in on whether Regenxbio may be granted a patent extension for its adeno-associated virus (AAV) technology used to produce Novartis’ blockbuster spinal muscular atrophy (SMA) therapy…

Continue ReadingUSPTO to Decide on Patent Extension for AAV Tech Used in Novartis’ Zolgensma

Protalix and Chiesi Report Positive Results From Fabry Disease Trial

  • Post author:PacConAdmin
  • Post published:March 21, 2022
  • Post category:Drug Industry Daily

The rare inherited condition Fabry Disease (FD) may soon have a new treatment. Source: Drug Industry Daily

Continue ReadingProtalix and Chiesi Report Positive Results From Fabry Disease Trial

BMS Sues AstraZeneca, Claiming Checkpoint Inhibitor Patent Infringement

  • Post author:PacConAdmin
  • Post published:March 21, 2022
  • Post category:Drug Industry Daily

Bristol Myers Squibb (BMS) is accusing AstraZeneca of infringing on several patents related to its blockbuster cancer immunotherapy Opdivo (nivolumab). Source: Drug Industry Daily

Continue ReadingBMS Sues AstraZeneca, Claiming Checkpoint Inhibitor Patent Infringement

EMA Panel Calls for Safety Updates for J&J’s, Moderna’s COVID-19 Vaccines

  • Post author:PacConAdmin
  • Post published:March 20, 2022
  • Post category:Drug Industry Daily

The European Medicines Agency’s (EMA) safety committee has recommended revised product safety information for Johnson & Johnson’s (J&J) and Moderna’s COVID-19 vaccines. Source: Drug Industry Daily

Continue ReadingEMA Panel Calls for Safety Updates for J&J’s, Moderna’s COVID-19 Vaccines

Biggest Decreases in Tau Predict Best Response to Aduhelm

  • Post author:PacConAdmin
  • Post published:March 20, 2022
  • Post category:Drug Industry Daily

Deep decreases from high baseline tau levels were associated with the best clinical response in patients who responded to Aduhelm during clinical trials, according to new data presented at the…

Continue ReadingBiggest Decreases in Tau Predict Best Response to Aduhelm

Democrats Push Biden to Issue Executive Orders on Drug Pricing, COVID-19 IP

  • Post author:PacConAdmin
  • Post published:March 20, 2022
  • Post category:Drug Industry Daily

There’s a push by congressional Democrats to get President Biden to issue a host of executive orders as soon as possible on key priorities, including drug pricing, because they’re not…

Continue ReadingDemocrats Push Biden to Issue Executive Orders on Drug Pricing, COVID-19 IP

Moderna and Pfizer Push for EUAs for Fourth Booster; Study Questions its Effectiveness

  • Post author:PacConAdmin
  • Post published:March 20, 2022
  • Post category:Drug Industry Daily

Moderna and Pfizer/BioNTech are both pushing to get expanded Emergency Use Authorization (EUA) for a fourth dose/second booster of their COVID-19 vaccines, but a new study questions its effectiveness in…

Continue ReadingModerna and Pfizer Push for EUAs for Fourth Booster; Study Questions its Effectiveness
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