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Amylyx: AdComm Decision Unlikely To Increase ALS Drug Approval - Vimarsana News

Amylyx: AdComm Decision Unlikely To Increase ALS Drug Approval

An FDA Advisory Committee will look at fresh data presented by ALS drug developer Amylyx (AMLX) as it attempts to secure accelerated approval. Read more here.

Cureus | Huntington's Disease: A Clinical Review - Vimarsana News

Cureus | Huntington's Disease: A Clinical Review

The Huntington's gene on chromosome 4 has a dominantly inherited CAG trinucleotide repeat expansion, ultimately resulting in Huntington's disease (HD), a completely penetrant neurological condition. The frequency is 10-100 times higher in the population descended from Europe than in East Asia. Through various processes, including impairment of proteostasis, transcription, and cell function, as well as direct toxicity of the mutant protein, mutated huntingtin triggers neuronal malfunction and loss at the cellular level. As the disease worsens, the brain becomes affected together with ...

Source: cureus.com
Patients with atopic dermatitis maintain positive outcomes with reduced dupilumab dosages - Vimarsana News

Patients with atopic dermatitis maintain positive outcomes with reduced dupilumab dosages

Patients with persistently controlled atopic dermatitis continued to experience stable and low disease activity after receiving reduced dosages of dupilumab, according to a study published in Allergy.These findings show that patient-centered dosing regimens can be successful, Lotte S. Spekhorst, MD, of the department of dermatology and allergology and National Expertise Center for Atopic

Source: healio.com
Can the Gold Coast Criteria for ALS Help Boost Clinical Trial Participation? - Vimarsana News

Can the Gold Coast Criteria for ALS Help Boost Clinical Trial Participation?

The utilization of the Gold Coast criteria for amyotrophic lateral sclerosis may in the recruitment of patients for clinical trials.

Investegate |Sanofi - Aventis Groupe Announcements | Sanofi - Aventis Groupe: Press Release: FDA approves Dupixent® (dupilumab) as first biologic medicine for children aged 6 months to 5 years with moderate-to-severe atopic dermatitis - Vimarsana News

Investegate |Sanofi - Aventis Groupe Announcements | Sanofi - Aventis Groupe: Press Release: FDA approves Dupixent® (dupilumab) as first biologic medicine for children aged 6 months to 5 years with moderate-to-severe atopic dermatitis

Investegate announcements from Sanofi - Aventis Groupe, Press Release: FDA approves Dupixent® (dupilumab) as first biologic medicine for children aged 6 months to 5 years with moderate-to-severe atopic dermatitis