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  • Science
    • PNH
    • Geographic Atrophy
    • C3G and Primary IC-MPGN
    • HSCT-TMA
    • Pipeline
  • Medical Research
    • Scientific Focus
    • Investigator Initiated Trials
    • Collaborative Research
    • Medical Writing Grants
    • Retina Fellow Research Grant
    • Exploratory Data Analysis
  • Congress & Manuscripts
    • Congress Presentations
    • Manuscripts
  • Resources
    • Medical Information
    • Early Access & Compassionate Use Program
    • Prescribing Information
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  • Search
  • This website is intended only for use by U.S. Healthcare Professionals.

Early Access & Compassionate Use Program

We are committed to developing innovative therapies for patients with serious diseases.

Clinical trials are a critical component of this effort, and they help to determine whether a new therapy is safe and effective. Until regulatory authorities make the decision 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 www.clinicaltrials.gov.

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 Compassionate Use program in the United States.  For any additional information please contact earlyaccess@apellis.com or submit a Compassionate Use request below.

COMPASSIONATE USE REQUEST

Report an Adverse Event or Product complaint

Please call 833-866-3346

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833-866-3346 (833-TO-MEDINFO)

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Geographic Atrophy Risk Calculator Important Usage Information

Intended Use

•  This Geographic Atrophy (GA) Risk Calculator is only intended for disease state awareness and for use by an eye doctor to understand the factors for disease progression. This is not a diagnostic tool or a tool to assist in treatment selection.

•  All decisions about patient care and diagnosis shall be made by a patient’s physician using his or her independent clinical judgment.

•  The GA Risk Calculator predicts a potential 5-year risk of outcomes for a GA patient (time to severe visual impairment (Snellen 20/200) and time to subfoveal involvement). This tool was developed utilizing risk equations using retrospective electronic health records of GA data from Cleveland Clinic patients (n=410). Statistical tests identified the most prominent predictors for time to severe visual impairment prediction as baseline visual acuity, subfoveal lesion, age, sex, smoking, fellow eye GA and select comorbidities. Validation was conducted using the Sham arms of Oaks (ClinicalTrials.gov, NCT03525613) and Derby (NCT03525600) trials. There is no treatment-related data incorporated in the tool nor is this tool intended to make any treatment assessments or recommendations.

•  The risk calculator being presented is for illustrative purposes only. Patient disease experience and/or progression may vary and depends on many individual factors including, but not limited to, the patient’s clinical history.

Limitations

•  Patients enrolled in clinical trials are expected to differ from those seen in routine clinical practice on important risk factors, such as time from GA onset and other severity measures.

•  More frequent data collection during clinical trials (monthly) than routine practice (~quarterly) could impact estimates of time to event outcomes.

•  The risk calculator predicts 5-year outcomes. However, the rate of progression on these outcomes can change with time within those 5-years.

•  These calculated predictions do not guarantee onset of identified outcomes.

Proceed to GA Risk Calculator

Developed by Apellis Pharmaceuticals, Inc. in collaboration with The Cleveland Clinic Foundation

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