An Amince da Sabon Binciken Asibiti don Maganin Farko-Mataki na Cutar Parkinson

A KYAUTA Kyauta 2 | eTurboNews | eTN
Written by Linda Hohnholz

A ranar 13 ga Janairu, 2022, Green Valley (Shanghai) Pharmaceuticals Co., Ltd. ta karɓi wasiƙar daga Hukumar Abinci da Magunguna ta Amurka (FDA) kan aikace-aikacen Sabbin Magunguna (IND) don gwajin gwaji na asibiti na duniya da yawa-II na Oligomannate (an kasuwa a matsayin "GV-971"), sabon magungunan kamfanin don magance cutar Alzheimer (AD). Wasiƙar ta nuna "Nazari na iya Ci gaba" tare da bincike na asibiti da aka ba da shawarar a cikin kula da marasa lafiya tare da cutar Parkinson na farko (PD). Kwanan aikin IND shine Disamba 16, 2021.

Wannan abun ciki na membobin SUBSCRIPTION KYAUTA ne kawai.
Shiga Yanzu shiga

A ranar 13 ga Janairu, 2022, Green Valley (Shanghai) Pharmaceuticals Co., Ltd. ta karɓi wasiƙar daga Hukumar Abinci da Magunguna ta Amurka (FDA) kan aikace-aikacen Sabbin Magunguna na Bincike (IND) don gwajin gwaji na asibiti na duniya da yawa-II na Oligomannate (wanda aka sayar da shi azaman "GV-971"), sabon magungunan kamfanin don magance cutar Alzheimer (AD). Wasiƙar ta nuna "Nazari na iya Ci gaba" tare da bincike na asibiti da aka ba da shawara a cikin kula da marasa lafiya masu ciwon Parkinson na farko (PD). Kwanan aikin IND shine Disamba 16, 2021.

Wannan abun ciki na membobin SUBSCRIPTION KYAUTA ne kawai.
Shiga Yanzu shiga

ABUBUWAN DA ZA KU GUDU DAGA WANNAN LABARI:

  • received the letter from the US Food and Drug Administration (FDA) on the Investigational New Drug (IND) application for the global multi-center phase-II clinical trial of Oligomannate (marketed as “GV-971”), the company’s innovative drug for treating Alzheimer’s disease (AD).
  • The IND effective date is December 16, 2021.
  • The letter indicated the “Study May Proceed”.

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Linda Hohnholz

Edita a shugaba don eTurboNews bisa ga eTN HQ.

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