Depression Symptom Experience Among Patients with Epilepsy Reporting a Diagnosis of Focal Seizures (FS): A Patient-Reported Outcomes Study
Joanne Wagner, Bhagyashree Oak, Brittany Smith, Amond Athavale, Alvin Ong, Cynthia Harden
At Xenon, we are focused on developing medicines that modulate ion channels to address neurological and psychiatric disorders. Our lead investigational candidate, azetukalner, is a Kv7 potassium channel opener in late-stage clinical development for multiple epilepsy indications (focal and generalized seizures) and depression (major depressive disorder and bipolar depression). Our early-stage pipeline leverages this same ion channel expertise to target chronic and acute pain and severe genetically defined epilepsies, like Dravet syndrome.

The AES Annual Meeting brings together healthcare providers, scientists, advocates, industry, and other professionals dedicated to better outcomes for people with epilepsy.
Saturday, December 6, 2025 | 12 PM ET – Monday, December 8, 2025 | 2 PM ET
Booths #133 and #233
A conversation focused on "Exploring Depression and Anxiety in Epilepsy: A Practical Dialogue with Patients and Providers"
Saturday, December 6, 2025
6 PM – 9 PM ET
Room B213
Sunday, December 7, 2025
2 PM – 5 PM ET
Room B305
Saturday, December 6, 2025
12 PM – 2 PM ET
Exhibit Hall B2, Poster Session 1
Joanne Wagner, Bhagyashree Oak, Brittany Smith, Amond Athavale, Alvin Ong, Cynthia Harden
Samuel Terman, Alving Ong, Tigwa Davis, Anthony Yu, Yecheng Huang, CJ Park, Dan Thorton
Danielle Becker, Jacqueline A. French, Jenny Qian, Lee Gervitz
Sunday, December 7, 2025
12 PM – 2 PM ET
Exhibit Hall B2, Poster Session 2
Alvin Ong, Joanne Wagner, Bhagyashree Oak, Brittany Smith, Amond Athavale, Cynthia Harden
John Stern, Danielle Becker, Steve Chung, Michael Macken, David King-Stephen, Andrew Zillgitt, Mohamad Koubeissi
Monday, December 8, 2025
12 PM – 1:45 PM ET
Exhibit Hall B2, Poster Session 3
Samuel Goodchild, Kristen Buford, Celine Dube, Samrat Thouta, Arjun Mahadevan, Matt Waldbrook, Alison Cutts, Megan Soriano, Maja Filipovic, Vishaal Rajani, Emily Hurley, Verner Lofstrand, Helen Clement, Davie Kim, Steven Wesolowski, James Empfield, JP Johnson Jr.
Jacqueline French, Roger Porter, Emilio Perucca, Martin Brodie, Cynthia Harden, Jenny Qian, Constanza Luzon Rosenblut, Christopher Kenney, Gregory N. Beatch
To meet a Medical Science Liaison (MSL) in your region, please fill out this form.
Hear from leading voices in the epilepsy field as they discuss current treatments and opportunities to improve patient care
We are actively enrolling patients in late-stage clinical trials across a spectrum of challenging neurological and psychiatric disorders, building upon promising Phase 2 data. This pivotal studies include:
Xenon Pharmaceuticals is committed to developing innovative, safe, and effective therapeutics to improve the lives of patients with neurological disorders, and we recognize the value of collaborating with patients, families, advocacy organizations, physicians and other healthcare professionals, researchers, and regulatory authorities to accomplish this goal.
We understand that patients, families, and physicians may be interested in accessing Xenon’s investigational drugs prior to regulatory approval through an expanded access program (sometimes referred to as “compassionate use program”). Expanded access programs allow patients with serious or immediately life‑threatening diseases, who have exhausted all other treatment options, to access an investigational drug outside of a clinical trial and prior to regulatory approval.
Xenon does not currently have an expanded access program that makes our investigational drugs available to patients other than by participating in one of our clinical trials. Clinical trials are controlled studies in humans designed to establish whether an investigational drug is safe and effective. Xenon believes clinical trials are the most appropriate way to efficiently collect all data necessary to seek regulatory approvals. At this time, Xenon does not have sufficient information about the potential risks and benefits of our investigational drugs to ensure that patient access outside the regulated clinical trial process does not delay or compromise our clinical trials and, ultimately, broad availability to the entire patient community.
Physicians, patients, and caregivers interested in learning more about Xenon’s ongoing clinical trials can find additional information at ClinicalTrials.gov.
Xenon may revise this policy at any time. If you have additional questions, please contact us at info@xenon-pharma.com.