2
ALL2
Regeneron PharmaceuticalsYear
2
ALL1
20241
2021DEALS // DEV.
2
ALL2
DevelopmentsCountry
2
ALL2
U.S.A2
ALL2
InapplicableTherapeutic Area
2
ALL1
Cardiology/Vascular Diseases1
Genetic DiseaseStudy Phase
2
ALL2
Approved FDFDeal Type
2
ALL2
InapplicableProduct Type
2
ALL2
AntibodyDosage Form
2
ALL1
Injection1
Subcutaneous InjectionLead Product
2
ALL2
AlirocumabTarget
2
ALL2
PCSK9Lead Product(s) : Alirocumab
Therapeutic Area : Cardiology/Vascular Diseases
Study Phase : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Praluent Injection Receives FDA Approval To Treat Children With Genetic High Cholesterol
Details : Praluent (alirocumab) inhibits the binding of PCSK9 to the LDL receptor. It is now approved for the treatment of pediatric patients aged 8 and older with heterozygous familial hypercholesterolemia.
Product Name : Praluent
Product Type : Antibody
Upfront Cash : Inapplicable
November 03, 2024
Lead Product(s) : Alirocumab
Therapeutic Area : Cardiology/Vascular Diseases
Highest Development Status : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : Alirocumab
Therapeutic Area : Genetic Disease
Study Phase : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
FDA Approves Add-on Therapy for Patients with Genetic form of Severely High Cholesterol
Details : The effectiveness and safety of Praluent were evaluated in a 12-week, double-blind, randomized trial among adult patients with HoFH. In the trial, 45 patients received 150 mg of Praluent every two weeks and 24 patients received a placebo.
Product Name : Praluent
Product Type : Antibody
Upfront Cash : Inapplicable
January 04, 2021
Lead Product(s) : Alirocumab
Therapeutic Area : Genetic Disease
Highest Development Status : Approved FDF
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable