Patients & Families

We are committed to our responsibility to seek innovation, understand the challenges faced by patients and their families, communicate with them clearly and openly, and to develop medicines that transform their lives.

Life with Angelman Syndrome: Small Victories, Big Impact

Small victories in improvements to motor skills can have a big impact for people living with Angelman syndrome and their families.

Life with Angelman Syndrome: The Impact of Sleep Deprivation

Angelman syndrome can cause severe sleep disturbance, not only for the person affected, but also for the rest of the family.

Life with Angelman Syndrome: Maintaining Focus & Concentration

For people living with Angelman syndrome, hyperactivity and anxiety are very common. Extreme emotions and over-excitement can be a struggle to manage.

“As wave is driven by wave
And each, pursued, pursues the wave ahead,
So time flies on and follows, flies, and follows,
Always, for ever and new. What was before
Is left behind; what never was is now;
And every passing moment is renewed.”

– Ovid, Metamorphoses


Using our BoldMedicine research expertise, we are focused on developing impactful medicines to transform the lives of people with rare neurological disorders.

We recognize that the responsibility of developing medicines for rare neurological disorders requires a boldness built on tenacity and optimism. For Ovid, the difference between drugs and medicine articulates the difference between product and purpose. Medicine is about enhancing health and treating conditions that can challenge everyday life.

Our goal is to transform the lives of our patients and their families though our BoldMedicine approach.

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Our People

Ovidians courageously take on the challenges and opportunities of drug development for rare neurological disorders with responsibility, agility and passion.

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