We care deeply about the needs and experiences of people with serious diseases and aim to champion the patient, caregiver, and community voice in everything we do.

To make the greatest impact, we are committed to listening and learning from patients, caregivers, and patient advocacy groups, and integrating their perspectives and insights into our decision-making.

Our goal is to be inclusive and representative of the communities we serve, and to develop clinical trials, therapies, and resources that consider the unique needs of patients. We value our collaborations with patient organizations and the patients and caregivers they represent, and are committed to an authentic, continuous, and transparent dialogue.

We are committed to developing innovative therapies for patients.

Clinical trials are a critical component of this effort, and help to determine whether a new therapy is safe and effective. Until regulatory authorities decide whether to approve a new therapy for a specific disease, it remains experimental and is generally not available to patients with that disease or condition outside of the clinical trials. If you would like to learn more about our clinical programs, visit:

We understand that there are critically ill patients who will not be eligible for available clinical trials and don’t have options for alternative therapies. In these circumstances, we will consider allowing access to the investigational therapy through Compassionate Use (CU) or an Early Access Program (EAP). CU is for an individual patient when no comparable or satisfactory alternative therapy options are available. An EAP is for a group of patients who have the same disease that was evaluated in clinical trials that we plan to submit to regulatory authorities in support of approval of the therapy. Both types of access programs require that the request for access to the drug is submitted by the treating physician and that the EAP & CU Core Principles are met:

EAP & CU Core Principles

• Providing access will not jeopardize either the clinical trials which determine whether the therapy is safe and effective, or regulatory pathways which make the decision whether to approve the therapy.
• The patient has a life-threatening disease and the physician believes there are no satisfactory alternative therapies on the market.
• The patient can potentially benefit from treatment and there is scientific evidence that the potential benefit outweighs risk to the patient’s safety.
• Providing access will not jeopardize the ability for Apellis to conduct essential tasks that are necessary to bring effective therapies to people suffering from the diseases we seek to treat.

Apellis has an active, global, Compassionate Use program. For any additional information please contact earlyaccess@apellis.com or submit a Compassionate Use request below.