Tweetovi

Blokirali ste korisnika/cu @AlbireoPharma

Jeste li sigurni da želite vidjeti te tweetove? Time nećete deblokirati korisnika/cu @AlbireoPharma

  1. Prikvačeni tweet
    30. sij

    We are pleased to announce the advancement of new programs for odevixibat, currently in development for the treatment of PFIC. We plan to initiate a pivotal trial in biliary atresia in 1H 2020 & plan a pivotal trial in Alagille syndrome by end of 2020.

    Poništi
  2. 4. velj

    is February 29, 2020. There are more than 7,000 rare diseases, affecting millions of people worldwide. Included among them are several rare cholestatic liver diseases that most have never heard of. Help us Liver Disease.

    Poništi
  3. 29. sij

    Albireo's Senior Director of Biostatistics Holly Huang had the honor of writing a review of the recently published book, Innovative Strategies, Statistical Solutions and Simulations for Modern Clinical Trials. Read it here:

    Poništi
  4. 28. sij

    "Her itch began in the evening and lasted all night. She would scratch herself until she bled." Listen to Claire's powerful account of her daughter Eleanor's journey w/ in our new video:

    Poništi
  5. 27. sij

    is quickly approaching! This year, the theme is – and for us, that means reframing perceptions around different rare liver diseases. We can’t wait to share more with you next month!

    Poništi
  6. 24. sij

    We know how valuable the patient voice is. This we are proud of the Alagille syndrome community for raising their voices & sharing their stories to increase awareness for those living w ALGS. Check out their video:

    Poništi
  7. 24. sij

    Pediatric hepatologist & namesake for Alagille syndrome, Daniel Alagille, was born on this day. Today we honor his discovery of this rare & raise the voices of those impacted. Learn more a/b Alagille syndrome:

    Poništi
  8. 24. sij

    Today (1/24) is the first-ever GLOBAL Alagille Syndrome Awareness Day! We are proud to support the & the ALGS community, including patients, caregivers, loved ones and those working to find new resources and options.

    Poništi
  9. 23. sij
    Poništi
  10. 22. sij

    Alex and Walter were at a loss when their son Armando was diagnosed with progressive familial intrahepatic cholestasis () at 3 months old – especially after finding out that a liver transplant might be necessary.

    Poništi
  11. 21. sij

    We are a proud supporter of the first-ever global Alagille Syndrome Awareness Day on January 24, 2020! works tirelessly to improve the lives of those living with Alagille syndrome, a rare disease that can impact the liver.

    Poništi
  12. 16. sij

    "I think that is why we're doing this. This is why we're here - to try and find better ways of looking after these children." - Professor Richard Thompson, pediatric hepatologist at in London and consultant to Albireo

    Poništi
  13. 14. sij

    Professor Richard Thompson, pediatric hepatologist at & consultant to Albireo has dedicated much of his life to studying rare cholestatic liver conditions & caring for those with . He offers us a unique perspective:

    Poništi
  14. 10. sij

    From advocating for her son Trey after his diagnosis to advocating for the entire PFIC community as co-leader of the PFIC Network, Tara Kearns has had a remarkable PFIC journey. shared her family’s story here:

    Poništi
  15. 7. sij

    Caring for a loved one with progressive familial intrahepatic cholestasis () is difficult enough – a lack of understanding of the and its symptoms adds an additional burden on PFIC families.

    Poništi
  16. 6. sij

    As an ICU , Emily Ventura knows how important a strong support system is for patients and their families. Read her story here:

    Poništi
  17. 3. sij

    For patients and caregivers, each day presents a new challenge to overcome. Uncertainty shapes the lives of parents like Alex and Walter whose son Armando was diagnosed with PFIC at 3 months old.

    Poništi
  18. 31. pro 2019.

    As we start a new decade, we are grateful for our team and all we've accomplished, and also excited for all that is coming in #2020. Our is to continue our commitment to helping people & families living w/ rare pediatric cholestatic .

    Poništi
  19. 31. pro 2019.

    Everyone has a story, but we're to the 8 PFIC families who bravely shared theirs. Our aspiration is that, through education and awareness, families living with rare liver disease can have hope for a brighter future. Thanks for looking back at . !

    Poništi
  20. 30. pro 2019.

    2019 was a big year for . Families stepped up to share their stories... and started a movement of raising global awareness for progressive familial intrahepatic cholestasis. is just getting started; we see you 2020!

    Poništi

Čini se da učitavanje traje već neko vrijeme.

Twitter je možda preopterećen ili ima kratkotrajnih poteškoća u radu. Pokušajte ponovno ili potražite dodatne informacije u odjeljku Status Twittera.

    Možda bi vam se svidjelo i ovo:

    ·