BioSpace looks at the 10 biggest drug approvals of 2021, headlined by Biogen’s Aduhelm (aducanumab) for Alzheimer’s disease and Pfizer and BioNTech’s COVID-19 vaccine Comirnaty.
Research Roundup: ADHD Drug Appears to Delay Alzheimer’s Symptoms and More
ADHD, Alzheimer’s disease, Brain, Clinical Trials, COVID-19 booster shots, Dementia, Exercise, HIV, Medical Journals, Memory, mRNA-1273/Moderna COVID-19 Vaccine (Moderna), Omicron (B.1.1.529) (South Africa), R&D, Therapeutics, Tuberculosis, TumorsResearchers at Emory investigated the use of an FDA-approved ADHD medication on patients with mild Alzheimer’s symptoms and found it appeared to reduce levels of tau.
Several studies point to promising new approaches to treating and preventing Alzheimer’s disease and a deeper understanding of how the disease progresses.
Eli Lilly is undertaking a strategic transformation that will result in the formation of new business units. The Indianapolis company’s Bio-Medicines unit will split into two separate businesses, with one focused on neuroscience and the other concentrated on immunology.
Eli Lilly and Company announced the launch of a head-to-head study to compare once-monthly injectable Emgality (galcanezumab-gnlm) with Nurtec ODT (rimegepant) for the prevention of migraine.
The U.S. Food and Drug Administration approved Biohaven Pharmaceutical Holding Company Ltd.’s Nurtec ODT (rimegepant 75 mg) for the preventive treatment of migraine. Nurtec ODT is indicated for adult patients with episodic migraine, e.g. those who experience less than 15 headache days per month.
Biogen and Capsigen forged a strategic collaboration to engineer novel adeno-associated virus (AAV) capsids that have the potential to become transformative gene therapies that treat underlying genetic causes of various central nervous system and neuromuscular disorders.
The U.S. Food and Drug Administration accepted AbbVie’s New Drug Application for atogepant, an investigational orally administered calcitonin gene-related peptide (CGRP) receptor antagonist for the preventive treatment of migraine in adults who meet criteria for episodic migraine.
The U.S. Food and Drug Administration accepted for review Impel NeuroPharma’s 5O5(b)(2) New Drug Application (NDA) for INP104 for the acute treatment of migraine headaches with or without aura in adults.
Biggest Novel Drug Approvals in 2020
"Bad" LDL Cholesterol, Acute Migraine, Antibodies, Coronavirus Disease (COVID-19) Pandemic, Coronavirus Disease 2019 (COVID-19), EvaluatePharma, FDA, Future Blockbusters, New Drug Approvals, Peanut Allergies, Relapsing Multiple Sclerosis (RMS), Spinal Muscular Atrophy (SMA), Therapeutics, Thyroid Eye Disease (TED), Triple Negative Breast Cancer (TNBC)BioSpace reviewed the top 10 novel drug approvals of 2020, loosely based on projected earnings in the upcoming years.