Total Orphan Drugs - Covering the Rare Disease Drug Industry

ALS Ice Bucket Challenge - Where Is The Money Going?

How to Start a Biotech: Fundraising and the Future of the Orphan Drug Industry

Gene Therapy Trial For Patients With Mechanical Heart Pumps Has Begun

The Top 20 Selling Orphan Drugs of 2020

Crowdfunding for Orphan Drug Research: Paving the Way for Early Stage Research on Rare Diseases

Team Of Indian Doctors Use 3D Printed Skull To Visualize Skull Before Surgery

FDA Approved Ruxolitinib Shown to Restore Hair Growth in Alopecia Patients

RedHill and RESprotect Sign a Deal Over Chemotherapy Drug

CureDuchenne to Provide Prosensa with $7 Million in Funding for Muscular Dystrophy Drug Research

The Perlstein Lab Raises $2 Million for the Production of Treatments for Rare Diseases

Drug Derived From Milk of Genetically Modified Rabbits to Treat Rare Swelling Disorder

Patient-Centered Clinical Trials Explained

Arena Pharmaceutical’s Pulmonary Arterial Hyeprtension Drug Receives Orphan Drug Status

Promedior’s Myelofibrosis Drug Receives FDA Orphan Drug Designation

The Next Global Child Health Care Priority: Pediatric Cancer Strategies

Insys Therapeutics Receives FDA Orphan Drug Designation for Cannabis Based Drug

FDA to Focus on Female Sexual Disorders at Upcoming Patient Meeting

Mirati Therapeutics Receives Orphan Designation for B-Cell Lymphoma Drug

AbbVie Granted Orphan Drug Status for Glioblastoma Therapy

British Prime Minister David Cameron Announces £300 Million Big Data Human Genome Database Project

BioMarin Sells FDA Priority Review Worth $67.5 Million

FDA Expands Approval of Imbruvica to Treat Chronic Lymphocytic Leukemia

Cystic Fibrosis Patients Sue Medicaid for Refusing Drug Kalydeco

Scotland’s New Rare Disease Action Plan

FDA Patient Focused Drug Development Initiative

Incorporating the patients perspective: Director of NORD Gives Recommendations at Capitol Hill Hearing

The ALS Ice Bucket Challenge: Effectively Raising Global Awareness for an Orphan Disease

Patient Group Victory in Muscular Dystrophy Drug Research

Genzyme Prices Gaucher Disease Drug at $310,250 a Year

Family Photo Scans: The Future of Rare Disease Diagnosis

Hepatitis C: Soon to Become a Rare Disease?

PTC Therapeutics Receives EU Approval for Muscular Dystrophy Drug

Evotec and Shire Team Up to Tackle Fabry’s Disease

KaloBios Ends Drug Development Deal with Sanofi Pasteur