Change Life Stories

Shanna, Oren and Damian Living with Hereditary Angioedema Type 1

There’s so much uncertainty with rare disease — the best treatment is your own confidence in making the decisions that are right for you.

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Nancy Living with ATTR Amyloidosis with Polyneuropathy

I look at my dad and think, ‘Is that what’s going to happen to me in the future?’

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Milton Living with ATTR Amyloidosis with Cardiomyopathy

When I think about memories, I smile. My memories keep me going.

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News Updates

March 26, 2025

Intellia Therapeutics Announces FDA Regenerative Medicine Advanced Therapy (RMAT) Designation Granted to Nexiguran Ziclumeran (nex-z) for the Treatment of Transthyretin (ATTR) Amyloidosis with Cardiomyopathy

March 4, 2025

Intellia Therapeutics Reports Inducement Grants under Nasdaq Listing Rule 5635(c)(4)

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Aiming to make the impossible, possible

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Transforming lives of people with severe diseases by developing potentially curative genome editing treatments.

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See how you can change life stories with genome editing.

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News Updates

Aiming to make the impossible, possible

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Full-Spectrum Approach

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