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Контент предоставлен Emma Nichols, PhD and Emma Hitt Nichols. Весь контент подкастов, включая эпизоды, графику и описания подкастов, загружается и предоставляется непосредственно компанией Emma Nichols, PhD and Emma Hitt Nichols или ее партнером по платформе подкастов. Если вы считаете, что кто-то использует вашу работу, защищенную авторским правом, без вашего разрешения, вы можете выполнить процедуру, описанную здесь https://ru.player.fm/legal.
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Ilaris for Gout, Generics for ADHD, Balversa for Urothelial Cancer, INO-3107 for Recurrent Respiratory Papillomatosis, Crovalimab for PNH

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Контент предоставлен Emma Nichols, PhD and Emma Hitt Nichols. Весь контент подкастов, включая эпизоды, графику и описания подкастов, загружается и предоставляется непосредственно компанией Emma Nichols, PhD and Emma Hitt Nichols или ее партнером по платформе подкастов. Если вы считаете, что кто-то использует вашу работу, защищенную авторским правом, без вашего разрешения, вы можете выполнить процедуру, описанную здесь https://ru.player.fm/legal.

In this week's New FDA Approval's podcast episode, Dr. Emma Hitt Nichols discusses the latest FDA approvals from August 28, 2023 – September 8, 2023. Please check back every Monday morning so that you can stay up to date.

Here is information on the latest US FDA approvals, the week of August 28 – September 8, 2023.

Check out our free downloads at nascentmc.com:

See the full write ups for today's episode at nascentmc.com/podcast

Here are the highlights:

  • Ilaris for Gout Flares in Adults: FDA approved Ilaris (canakinumab) for adult gout flares when other treatments failed; previously approved for CAPS and other diseases.
  • Generics of ADHD Medication: FDA approved several generic versions of Vyvanse; Takeda's patent expired; medication was in short supply due to manufacturing issues.
  • sNDA for Balversa in mUC: Janssen submitted sNDA for Balversa for urothelial carcinoma patients with specific genetic alterations; previously granted accelerated approval in 2019.
  • INO-3107 for RRP: FDA granted Breakthrough Therapy designation for INO-3107 for recurrent respiratory papillomatosis caused mainly by HPV-6/11; Inovio to initiate a trial in 2024.
  • Crovalimab for PNH: FDA accepted BLA for crovalimab as a treatment for PNH based on positive Phase III study results; potential approval expected late 2023/early 2024.
  • Intro and outro music

Garden Of Love by Pk jazz Collective

  continue reading

60 эпизодов

Artwork
iconПоделиться
 

Fetch error

Hmmm there seems to be a problem fetching this series right now. Last successful fetch was on July 29, 2024 20:37 (3M ago)

What now? This series will be checked again in the next hour. If you believe it should be working, please verify the publisher's feed link below is valid and includes actual episode links. You can contact support to request the feed be immediately fetched.

Manage episode 407556908 series 3561458
Контент предоставлен Emma Nichols, PhD and Emma Hitt Nichols. Весь контент подкастов, включая эпизоды, графику и описания подкастов, загружается и предоставляется непосредственно компанией Emma Nichols, PhD and Emma Hitt Nichols или ее партнером по платформе подкастов. Если вы считаете, что кто-то использует вашу работу, защищенную авторским правом, без вашего разрешения, вы можете выполнить процедуру, описанную здесь https://ru.player.fm/legal.

In this week's New FDA Approval's podcast episode, Dr. Emma Hitt Nichols discusses the latest FDA approvals from August 28, 2023 – September 8, 2023. Please check back every Monday morning so that you can stay up to date.

Here is information on the latest US FDA approvals, the week of August 28 – September 8, 2023.

Check out our free downloads at nascentmc.com:

See the full write ups for today's episode at nascentmc.com/podcast

Here are the highlights:

  • Ilaris for Gout Flares in Adults: FDA approved Ilaris (canakinumab) for adult gout flares when other treatments failed; previously approved for CAPS and other diseases.
  • Generics of ADHD Medication: FDA approved several generic versions of Vyvanse; Takeda's patent expired; medication was in short supply due to manufacturing issues.
  • sNDA for Balversa in mUC: Janssen submitted sNDA for Balversa for urothelial carcinoma patients with specific genetic alterations; previously granted accelerated approval in 2019.
  • INO-3107 for RRP: FDA granted Breakthrough Therapy designation for INO-3107 for recurrent respiratory papillomatosis caused mainly by HPV-6/11; Inovio to initiate a trial in 2024.
  • Crovalimab for PNH: FDA accepted BLA for crovalimab as a treatment for PNH based on positive Phase III study results; potential approval expected late 2023/early 2024.
  • Intro and outro music

Garden Of Love by Pk jazz Collective

  continue reading

60 эпизодов

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