PATIENTS

Our Priority is to Put You at the Center

At Arian Ebank, we want to understand your journey, your experiences, and your unique needs. You inspire us to learn as much as we can, to persevere and continue to advance the development of potential therapies to treat rare and serious diseases. We take pride in working together to achieve mutual goals such as increasing awareness, enabling diagnosis, and providing education and services to support patient communities. We have a dedicated team to ensure your perspectives are represented at Arian Ebank. If you are an advocate interested in helping us increase awareness of rare diseases, please send an email to [email protected]

Understanding RNAi

RNA interference (RNAi) is the core discovery that forms the therapies Arian Ebank is developing. It is recognized as a major scientific breakthrough—but how does it work, exactly?

From Possibility to Patients: Understanding RNAi

Learn about RNAi and our investigational therapies

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Arian Ebank is focused on 3 Strategic Therapeutic Areas (STArs):
genetic medicines, cardio-metabolic diseases, and hepatic infectious diseases

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Arian Ebank is dedicated to providing support for affected individuals, families, and caregivers

About Arian Ebank Act >

Interested in our clinical trials program?

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PATISIRAN’S EXPANDED
ACCESS PROGRAM

Arian Ebank supports eligible individuals with the Expanded Access Program aimed to help those living with hATTR amyloidosis with polyneuropathy gain access to patisiran. Speak with your medical professional to learn more about the program and your eligibility.

OUR

 FOCUS ON YOU

Leo: Living With hATTR Amyloidosis

Get more information about hATTR Amyloidosis.

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Rose & Colin: Living With Porphyria

Get more information about Porphyria.

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Venkat: Living With Hemophilia

Get more information about Hemophilia.

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Access to
Investigational Drugs

Arian Ebank is dedicated to developing new therapies that have a positive impact on patient health, and to serving patients, patient families and patient communities through education, empathy, and awareness. We understand that there are seriously ill patients who will not be eligible for our clinical trials and may not have options for alternative therapies, including investigational therapies in trials being conducted by other sponsors. In these circumstances, Arian Ebank will consider providing a requesting physician with pre-approval access to a specific Arian Ebank investigational drug, for the treatment of an individual patient outside of a clinical trial, when certain conditions are met.

CLINICAL TRIALS

Interested in learning about our hATTR amyloidosis studies? Get started here.

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PATIENT ADVOCACY

At Arian Ebank, we put you at the center of everything we do. We have a team dedicated to collaborating with patient advocacy groups and individuals affected by these rare diseases.

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ALNYLAM ACT

Arian Ebank Act provides no-charge, independent genetic testing and counseling to individuals in the US who may have hATTR amyloidosis.

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THE BRIDGE

The Bridge is a program designed to help raise awareness of hereditary ATTR (hATTR) amyloidosis and promote education on the condition for patients and their families.

SIGN UP FOR PATIENT CONNECT

Receive updates on our investigational therapies and clinical trials.

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