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FDA Grants Lin BioScience Rare Pediatric Disease Status for LBS-008 to Treat Stargardt Disease.

M2 PHARMA-September 18, 2018-FDA Grants Lin BioScience Rare Pediatric Disease Status for LBS-008 to Treat Stargardt Disease


- The US Food and Drug Administration has granted Rare Pediatric Disease designation to LBS-008, a first-in-class oral therapy for the treatment of Stargardt Disease, US-based drug development company Lin BioScience said.

The Priority Review Voucher Program is intended to encourage development of therapies to prevent and treat rare pediatric diseases.

If LBS-008 is approved by the FDA for Stargardt Disease, the RPD designation qualifies Lin BioScience for the Priority Review Voucher.

The voucher, which can be sold or transferred to another entity, can be used by the sponsor to receive Priority Review for a future NDA or BLA submission and reduce the candidate's FDA review time to six months.

LBS-008 is a first-in-class oral therapy that prevents the buildup of toxins in the eye that cause Stargardt Disease and atrophic Age-related Macular Degeneration (dry AMD).

The NIH's Blueprint Neurotherapeutics Network, which funded the therapy's discovery and development, provides support and funding through to the completion of Phase I clinical trials.

LBS-008 received both US and EU orphan drug designation in 2017 and 2018, respectively.

Stargardt Disease is an untreatable inherited condition that causes permanent vision loss in children during childhood and adolescence.

This rare disease is caused by a mutation in the ABCA4 gene, which leads to the accelerated formation and accumulation of toxic vitamin A dimers in the retina that cause progressive retinal cell death and permanent loss of vision.

Lin BioScience, Inc. is a drug development company targeting untreatable diseases. Its therapeutic pipeline, which includes two candidates with Orphan Drug Status, is focused on meeting the unmet needs of patients suffering from cancer, macular degeneration, liver disease and diabetes.

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Publication:M2 Pharma
Date:Sep 18, 2018
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