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QED Therapeutics focuses on creating meaningful therapies for individuals with skeletal dysplasias, particularly achondroplasia and hypochondroplasia. They are currently involved in clinical trials to advance their investigational therapy, infigratinib.
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An investigational therapy for achondroplasia that has received breakthrough therapy designation from the FDA.
Programs such as the PROPEL Infant & Toddler trial and ACCEL observational study for children with achondroplasia and hypochondroplasia.
Infigratinib is the first and only investigational therapy for achondroplasia awarded breakthrough therapy designation by the FDA.
Children with achondroplasia from birth to less than 3 years old can enroll in the PROPEL Infant & Toddler trial.
QED Therapeutics is dedicated to treating skeletal dysplasias, specifically achondroplasia and hypochondroplasia.