From Cystic Fibrosis Foundation <[email protected]>
Subject Together: a Community Update
Date January 13, 2022 9:20 PM
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The latest information for January 13, 2022


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Thursday, January 13, 2022

You're Invited to our National Annual Meeting

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We all dream of the day when CF stands for Cure Found. Join us Thursday, January 27 at 8 p.m. ET for our second National Annual Meeting ([link removed]) to hear from President and CEO Michael Boyle, MD, as we celebrate the progress made in 2021 and hear his vision for this year. You will also have the chance to ask Foundation leaders your questions about our ongoing efforts to advance a cure for CF, support the community, and provide high-quality care. We hope you can join us!

Save your seat today » ([link removed])

What's New In Cystic Fibrosis Research

We are excited to kick off the new year with several funding awards for the development of potential treatments for people living with cystic fibrosis.

We awarded $5 million BiomX ([link removed]) to conduct a Phase 1b/2a clinical trial for a potential phage therapy in Pseudomonas aeruginosa infections.

To study the potential use of inhaled colistin as an additional option to treat Pseudomonas aeruginosa infections, we awarded $4.7 million to EnBiotix Inc ([link removed]).

As part of our Path to a Cure initiative, we invested in SalioGen Therapeutics ([link removed]) to support preclinical research into a novel genetic therapy that could benefit everyone with cystic fibrosis, regardless of their mutation.

Finally, we awarded up to $3.5 million to Arrevus Inc. ([link removed]) to test a potential treatment for pulmonary exacerbations in a late phase clinical trial.

Our vision is a cure for every person with cystic fibrosis and a life free from the burden of this disease. We will not leave anyone behind.

How I Learned to Let Go as a Parent of a Child with CF

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As Abby Alten Schwartz's daughter became a teenager, she found it difficult to let her manage more of her cystic fibrosis care on her own. With the help of a therapist, Abby shares how she learned it wasn ([link removed]).

Read Abby ([link removed])

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Cystic Fibrosis Foundation
4550 Montgomery Ave, Suite 1100N
Bethesda, Maryland 20814

www.cff.org ([link removed])



4550 Montgomery Avenue, Suite 1100N | Bethesda, MD 20814 US

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