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National Family Caregivers Month: Shining a Light on Jessica’s Story

This summer we shared the powerful story of LuPita, currently living with dementia. Today we are honored to introduce Jessica, LuPita’s daughter and care partner, in honor of November marking National Family Caregivers Month. Hear firsthand from Jessica on how she decided to take on the vital role, the importance of taking care of oneself […]

Meet our new CDO: Chad J. Swanson, Ph.D., Chief Development Officer answers questions about his career and the Prothena team

This month, we’re excited to hear from the newest member of our leadership team at Prothena! In September, Chad Swanson was appointed as Prothena’s new Chief Development Officer. A neuropharmacologist with over 20 years industry experience, Chad joined Prothena as Senior Vice President and Head of Clinical Development in January 2023. In his new role, […]

World Amyloidosis Day: Shining a Light on Steve’s Story

Tomorrow marks World Amyloidosis Day, and we at Prothena are proud to join the Amyloidosis Alliance to help raise awareness of amyloidosis, a complex disease often misunderstood and misdiagnosed by medical professionals and unheard of by the general public. In the below video, Steve, living with AL amyloidosis, talks about the difficult and long journey […]

It’s not a sprint… Christie Nie M.D. MSc. Vice President, Global Clinical Development answers questions about her career and Prothena’s clinical development team

From running marathons to developing potential breakthrough treatments, for Christie it’s all about perseverance At Prothena, our mission is to bring life-changing therapies to patients battling neurodegenerative and rare peripheral amyloid diseases. Our clinical development efforts play a vital role in moving these therapies from early research to potential treatments that could improve the lives […]

World Alzheimer’s Day: Shining a Light on Phil’s Story

Saturday, on World Alzheimer’s Day, we at Prothena joined Alzheimer’s Disease International to raise awareness of Alzheimer’s disease and challenge the stigma of this disease and other dementias. We recently shared the story of LuPita, currently living with dementia. Today, we are honored to help Phil tell his story. In another powerful tale, Phil underscores […]

Alzheimer’s Disease International CEO Paola Barbarino answers questions about the organization’s work in dementia and Alzheimer’s disease

Alzheimer’s disease is a devastating form of dementia that causes memory, thinking and behavior problems. It is believed two different proteins – Aβ (amyloid beta) and tau – are the primary contributors to its pathology. Misfolded Aβ builds up to form plaques between nerve cells in the brain. Tangles of twisted tau fibrils spread from […]

On putting the puzzle pieces together: the long journey to an AL amyloidosis diagnosis

Earlier this year, we heard advice for people living with AL amyloidosis from an AL amyloidosis patient herself, Linda. Today, we continue to elevate firsthand perspectives of people directly impacted by this rare disease. Hear from Donna, a wife and mother, and caregiver to her husband Mike who is living with AL amyloidosis. She describes […]

Carol Karp, Chief Regulatory Officer, answers questions about her career and Prothena’s regulatory team

Prothena is committed to developing novel and transformative medicines to create a better future for patients with neurodegenerative and rare peripheral amyloid diseases, which affect millions of people and their families worldwide. Before any treatment is made available to patients in the U.S., it must go through a rigorous set of clinical and nonclinical testing […]

The Longest Day: Shining a Light on LuPita’s Story

  Today marks The Longest Day. It’s the summer solstice and the day with the most sunlight all year long. Also today, we stand with the Alzheimer’s community to fight the darkness of Alzheimer’s disease and all other dementias. There has been remarkable progress in the treatment of Alzheimer’s disease in the past few years, […]

A novel mechanism of action to address unmet needs in AL amyloidosis

AL amyloidosis, a rare, progressive and often fatal disease, occurs when a type of immune cell, called plasma cells, produce high levels of an abnormal protein called light chain that misfolds and clumps together to form aggregated amyloid which the body cannot break down. Clumped together, the amyloid can travel through blood vessels, damaging cells […]