-
Categories
-
Pharmaceutical Intermediates
-
Active Pharmaceutical Ingredients
-
Food Additives
- Industrial Coatings
- Agrochemicals
- Dyes and Pigments
- Surfactant
- Flavors and Fragrances
- Chemical Reagents
- Catalyst and Auxiliary
- Natural Products
- Inorganic Chemistry
-
Organic Chemistry
-
Biochemical Engineering
- Analytical Chemistry
-
Cosmetic Ingredient
- Water Treatment Chemical
-
Pharmaceutical Intermediates
Promotion
ECHEMI Mall
Wholesale
Weekly Price
Exhibition
News
-
Trade Service
On September 7, 2021, Alnylam Pharmaceuticals announced the latest results obtained in a phase 3 clinical trial of its RNAi drug vutrisiran in the treatment of patients with transthyretin-mediated (ATTR) amyloidosis
Hereditary transthyretin-mediated (hATTR) amyloidosis is a hereditary and progressive debilitating and fatal disease caused by mutations in the TTR gene
Vutrisiran is a subcutaneously administered RNAi therapeutic drug that is being developed to treat ATTR amyloidosis, including hATTR and wild-type ATTR (wtATTR) amyloidosis
▲Introduction of Onpattro and vutrisiran (picture source: Alnylam official website)
The data obtained this time further supports the primary and secondary endpoint results previously reported in the HELIOS-A trial, which was carried out in 164 patients with hATTR amyloidosis with polyneuropathy
The results of data analysis showed that at the 9th month, the trial reached the primary endpoint and all secondary endpoints
In terms of safety, compared with placebo, vutrisiran showed encouraging safety and tolerability characteristics
Reference materials:
Reference materials:[1] Alnylam Presents Additional 9-Month Data from HELIOS-A Phase 3 Study of Vutrisiran at the European ATTR (EU-ATTR) Amyloidosis Meeting.
[1] Alnylam Presents Additional 9-Month Data from HELIOS-A Phase 3 Study of Vutrisiran at the European ATTR (EU-ATTR) Amyloidosis Meeting.
Retrieved September 7, 2021, from https:// home/20210907005432/en