Researchers Find that Disturbances in the Body’s Internal Clock Increase the Risk of Parkinson’s Disease Threefold

According to a recent article in Parkinson’s News Today, researchers at the UCSF Weill Institute discovered that disturbances in circadian rhythm increased a person’s risk of Parkinson's disease threefold. Circadian…

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New Meniere’s Disease Treatment Has FDA Approval to Advance to a Phase III Trial

Sound Pharmaceuticals announced the first-ever Phase III clinical trial protocol for Meniere’s disease to be approved by the FDA. Meniere’s disease (MD) is a neurotologic disorder that involves tinnitus (ringing…

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Oral Octreotide Approved to Treat Acromegaly
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Oral Octreotide Approved to Treat Acromegaly

As shared in Medscape, the FDA recently approved oral octreotide (Mycapssa) for the treatment of patients with acromegaly. These delayed-release capsules are the first approved oral somatostatin analog ever approved.…

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UK Moves to Make Whole Genome Sequencing Standard in the NHS, Improving Diagnosis for Rare Disease Patients

A recent study has demonstrated that through standardizing the whole genome sequencing process and making it routine for patients, we can improve rare disease diagnosis across the board. Earlier diagnosis…

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Positive Results from Trial of Sotatercept, a Treatment for Pulmonary Arterial Hypertension
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Positive Results from Trial of Sotatercept, a Treatment for Pulmonary Arterial Hypertension

Acceleron Pharma has released the results from Phase 2 of their PULSAR trial, which studied sotatercept as a treatment for pulmonary arterial hypertension. Researchers are very excited by the positive…

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Botox is on Its Way to Become a New Therapeutic Option for Children with Neurogenic Detrusor Overactivity

Botox Botox was first approved as a treatment for strabismus and blepharospasm, rare eye conditions, in 1989. Now, it is approved for 11 different conditions including cervical dystonia, chronic migraines,…

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A New Partnership will Advance Exosome-Based Gene Therapy for Neuromuscular Diseases
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A New Partnership will Advance Exosome-Based Gene Therapy for Neuromuscular Diseases

By engineering exosomes, Sarepta Therapeutics believes they can utilize gene therapies, RNA therapies, and gene editing without triggering an immune response in the body. They have just announced a new…

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FDA Approves CRYSVITA for Tumor-Induced Osteomalacia
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FDA Approves CRYSVITA for Tumor-Induced Osteomalacia

Ultragenyx Pharmaceutical's therapy, CRYSVITA, has recently been approved by the FDA for the treatment of FGF23-related hypophosphatemia in tumor-induced osteomalacia (TIO) associated with phosphaturic mesenchymal tumors. This approval comes after…

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