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ImprimisRx Gets Form 483 for Unsanitary Conditions, Drug Quality Issues

  • Post author:PacConAdmin
  • Post published:November 14, 2022
  • Post category:Drug Industry Daily

The FDA issued a nine-observation Form 483 to ImprimisRx’s Ledgewood, N.J., facility for unsanitary conditions and other deficiencies observed during a July 11 to Aug. 5 inspection. Source: Drug Industry…

Continue ReadingImprimisRx Gets Form 483 for Unsanitary Conditions, Drug Quality Issues

Indivior to Acquire Overdose-Reversal Drugmaker Opiant Pharmaceuticals

  • Post author:PacConAdmin
  • Post published:November 14, 2022
  • Post category:Drug Industry Daily

Richmond, Va.-based Indivior, maker of the opioid treatment Suboxone (buprenorphine-naloxone), has announced plans to purchase Opiant Pharmaceuticals, a Santa Monica, Calif., producer of the opioid overdose nasal spray Narcan (naloxone),…

Continue ReadingIndivior to Acquire Overdose-Reversal Drugmaker Opiant Pharmaceuticals

Oregon AG Sues Four Pharma Companies for Blocking AndroGel Competitors

  • Post author:PacConAdmin
  • Post published:November 14, 2022
  • Post category:Drug Industry Daily

The Oregon Attorney General has filed a lawsuit accusing four pharmaceutical companies of filing sham lawsuits to prevent competitors from bringing a lower-priced generic version of their drug to market.…

Continue ReadingOregon AG Sues Four Pharma Companies for Blocking AndroGel Competitors

In Another Alzheimer’s Flop, Gantenerumab Fails Twin Phase 3 Trials

  • Post author:PacConAdmin
  • Post published:November 14, 2022
  • Post category:Drug Industry Daily

Roche and its Genentech subsidiary announced disappointing topline data from twin phase 3 trials of their antiamyloid antibody, gantenerumab, for treating Alzheimer’s. Source: Drug Industry Daily

Continue ReadingIn Another Alzheimer’s Flop, Gantenerumab Fails Twin Phase 3 Trials

Appco Pharma Gets Form 483 for Missing Records

  • Post author:PacConAdmin
  • Post published:November 11, 2022
  • Post category:Drug Industry Daily

Appco Pharma’s Piscataway, N.J. generic drug manufacturing facility was dinged by the FDA for lacking temperature and humidity records for some equipment and other documentation lapses listed in a five-observation…

Continue ReadingAppco Pharma Gets Form 483 for Missing Records

FDA Pushes Back Comment Period on IRB, Informed Consent Rules Until End of Year

  • Post author:PacConAdmin
  • Post published:November 11, 2022
  • Post category:Drug Industry Daily

In response to requests for a later deadline, the FDA has granted more time to comment on a pair of long-awaited proposed rules on institutional review board (IRB) reviews and…

Continue ReadingFDA Pushes Back Comment Period on IRB, Informed Consent Rules Until End of Year

GSK to Restrict Ovarian Cancer Drug’s Indication

  • Post author:PacConAdmin
  • Post published:November 11, 2022
  • Post category:Drug Industry Daily

The FDA has asked GSK to restrict its second-line maintenance indication for its ovarian cancer drug Zejula (niraparib) to patients with deleterious or suspected deleterious germline BRCA mutations, maintaining approval…

Continue ReadingGSK to Restrict Ovarian Cancer Drug’s Indication

FTC Challenges Abuse of FDA’s Orange Book to Block Drug Competition

  • Post author:PacConAdmin
  • Post published:November 11, 2022
  • Post category:Drug Industry Daily

The Federal Trade Commission (FTC) has filed an amicus brief in the U.S. District Court for the District of Delaware arguing that some branded drug manufacturers have a history of…

Continue ReadingFTC Challenges Abuse of FDA’s Orange Book to Block Drug Competition

FDA Seeks Comment on ICH Draft Guidance on Viral Safety of Biotechnology Products

  • Post author:PacConAdmin
  • Post published:November 10, 2022
  • Post category:Drug Industry Daily

The FDA is seeking public comment on an International Council for Harmonisation (ICH) draft guidance that describes risk-based principles and mitigation strategies to assure viral safety in biotechnology products from…

Continue ReadingFDA Seeks Comment on ICH Draft Guidance on Viral Safety of Biotechnology Products

EQRx Drops US Plans for Sugemalimab as NSCLC Therapy

  • Post author:PacConAdmin
  • Post published:November 10, 2022
  • Post category:Drug Industry Daily

EQRx Therapeutics is dropping its U.S. developmental efforts for sugemalimab plus chemotherapy, a combination it was working on as a treatment for stage IV nonsmall cell lung cancer (NSCLC). Source:…

Continue ReadingEQRx Drops US Plans for Sugemalimab as NSCLC Therapy
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