NULIBRY™ (fosdenopterin)


Approved for Use in the U.S.

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Prescribing Information

In 2022, Sentynl Therapeutics, Inc. acquired global rights to NULIBRY and is responsible for the ongoing development and commercialization of NULIBRY in the U.S. and developing, manufacturing and commercializing fosdenopterin globally.

our products

It is our mission to develop transformative medicines to treat patients who suffer from genetic diseases and cancers with clear genetic drivers. We prioritize focused execution to reach patients in need of options quickly while also strategically advancing high-quality programs in our pipeline. Every approved product from BridgeBio represents our commitment to delivering hope through rigorous science.