Facebook-f Twitter Instagram Podcast Youtube Tiktok Linkedin-in Pinterest Envelope Share
SHARE YOUR STORY!
  • About
    • Meet Our Contributors
    • Meet Our Partners
    • Meet the Patient Worthy Team
    • Collaborative Content On Patient Worthy
  • Diseases
  • Share Your Story
    • Patient Worthy Content Submission Guidelines
    • Patient Worthy Writing Prompts
    • Submit Your Story
    • Patient Stories
  • Resources
    • Library
    • Events
    • Patient Worthy FAQs
  • Podcast
  • Contact
Menu
  • About
    • Meet Our Contributors
    • Meet Our Partners
    • Meet the Patient Worthy Team
    • Collaborative Content On Patient Worthy
  • Diseases
  • Share Your Story
    • Patient Worthy Content Submission Guidelines
    • Patient Worthy Writing Prompts
    • Submit Your Story
    • Patient Stories
  • Resources
    • Library
    • Events
    • Patient Worthy FAQs
  • Podcast
  • Contact
  • Join PW

32 Search Results Found

You searched for: "primary+hyperoxaluria"
  1. Home>
  2. Search results for “primary+hyperoxaluria”>
  3. Page 2
New Treatment for Primary Hyperoxaluria Type 1 Approved in Europe

New Treatment for Primary Hyperoxaluria Type 1 Approved in Europe

According to a story from Fierce Pharma, the drug company Alnylam Pharmaceuticals has seen its investigational therapy lumasiran (marketed as Oxlumo) recently gain approval for use in the EU as…

Continue Reading New Treatment for Primary Hyperoxaluria Type 1 Approved in Europe
Phase 3 Study Results Bring Hope for Children with Primary Hyperoxaluria Type 1  

Phase 3 Study Results Bring Hope for Children with Primary Hyperoxaluria Type 1  

  According to a recent article in BioSpace, young children and infants who have been diagnosed with primary hyperoxaluria type 1 (PH1) are often faced with the use of gastrostomy…

Continue Reading Phase 3 Study Results Bring Hope for Children with Primary Hyperoxaluria Type 1  
An Experimental Treatment for Primary Hyperoxaluria has Earned Rare Pediatric Disease Designation

An Experimental Treatment for Primary Hyperoxaluria has Earned Rare Pediatric Disease Designation

According to a story from BioSpace, the biopharmaceutical company Dicerna Therapeutics, Inc. has announced recently that the US Food and Drug Administration (FDA) has granted Rare Pediatric Disease designation to…

Continue Reading An Experimental Treatment for Primary Hyperoxaluria has Earned Rare Pediatric Disease Designation
Living With Primary Hyperoxaluria: A Rare Patient Story

Living With Primary Hyperoxaluria: A Rare Patient Story

Molly Ouimet was three years old when she got her first kidney stone. Molly, who wasn't very vocal at the time, had a difficult time explaining the pain that she…

Continue Reading Living With Primary Hyperoxaluria: A Rare Patient Story
Alnylam Seeks FDA Approval for First Treatment of Primary Hyperoxaluria Type 1

Alnylam Seeks FDA Approval for First Treatment of Primary Hyperoxaluria Type 1

Copyscape score: 2% Alnylam has recently completed the third phase of their clinical trial of lumasiran, which was created for the treatment of primary hyperoxaluria type 1 (PH1). While they…

Continue Reading Alnylam Seeks FDA Approval for First Treatment of Primary Hyperoxaluria Type 1
Patients with Primary Hyperoxaluria Type 2 Are Reminded to Carefully Follow Up

Patients with Primary Hyperoxaluria Type 2 Are Reminded to Carefully Follow Up

A new joint clinicial investigation has come out with a reminder to patients with primary hyperoxaluria type 2 (PH2) to adherr to the requirements regarding careful follow up proceedings. This…

Continue Reading Patients with Primary Hyperoxaluria Type 2 Are Reminded to Carefully Follow Up
Pediatric Clinical Trial Initiated for Primary Hyperoxaluria Type 1!

Pediatric Clinical Trial Initiated for Primary Hyperoxaluria Type 1!

Alnylam Pharmaceuticals has been developing lumasiran as a potential treatment for primary hyperoxaluria type 1 (PH1). This investigation began with ILLUMINATE-A, a clinical trial whose results should be announced by…

Continue Reading Pediatric Clinical Trial Initiated for Primary Hyperoxaluria Type 1!
New Updates on Studies of Lumasiran in Patients With Primary Hyperoxaluria Type 1

New Updates on Studies of Lumasiran in Patients With Primary Hyperoxaluria Type 1

Alnylam has provided updates about their programs for patients with primary hyperoxaluria type 1 (PH1), a rare condition that affects the kidneys and bladder. As part of their Alnylam Act® program,…

Continue Reading New Updates on Studies of Lumasiran in Patients With Primary Hyperoxaluria Type 1
  • Go to the previous page
  • 1
  • 2
  • 3
  • 4
  • Go to the next page

Featured


Picture of Family


Metastatic Breast Cancer: Navigating Grief


Picture of Ralph Family walking


Rethinking What It Means to Live With Acromegaly


Illustration of mentor program members


The Let’s Chat CAR T One-on-One Mentor Program: Speaking with Someone Who Understands What You Are Going Through

SHARE YOUR STORY!
We believe rare disease patients are people, not a diagnosis. Through education, awareness and some humor, we help patients, caregivers and support persons by providing relevant and often inspirational news and stories.
Our goals are to share stories, cultivate strong community, provide the latest medical findings, connect people and pioneer production of patient worthy information. Help us attain these goals by telling us a little bit about yourself!

Let’s Work Together!

Partner With Us
Submit a Story

Keep Up to Date

Subscribe to Our Newsletter
Check Out Rare Events
Get Inspired By Our Memes

Learn More

About Us
Rare Diseases and Conditions
Terms of Use
Privacy Notice
Privacy Policy for CA Residents
EU/UK Privacy Notice
Data Privacy Framework: Consumer Privacy Policy
Consumer Health Data Privacy Policy
Cookie Notice

Facebook-f Twitter Instagram Podcast Youtube Tiktok Linkedin-in Pinterest Envelope

© Copyright 2024 Patient Worthy

Sign Up With a Patient Worthy Account and Share Your Rare Story

- OR -

Sign Up For Our Patient Panel

Make a difference, share your experiences and get paid. Opt-in and join Patient Worthy's panel for paid opportunities such as surveys, market research, patient advisory panels and more.

More Info

We're Happy You're Here!

What best describes you when it comes to rare disease? (check all that apply)

What rare disease(s)/conditions are most important to you?

Visit Home Page or

Thank you for signing up for a Patient Worthy Account!

Have a rare disease story to share? Let us know

Share Story

- OR -

Sign Up For Our Patient Panel

Make a difference, share your experiences and get paid. Opt-in and join Patient Worthy's panel for paid opportunities such as surveys, market research, patient advisory panels and more.

More Info