http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2019255068-A1

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filingDate 2017-09-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d424a3faa462de8db1e3e92eb3308d22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4aacfc95dee5513d6fdf0ff8aaba57a2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c1a71562c1ecc9ddb98fdcfd0b5703b0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f9d8df60bb5742cdfce35293c4574b9c
publicationDate 2019-08-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2019255068-A1
titleOfInvention Prostacyclin analogue formulations
abstract The present invention relates to an injectable pre-formulation comprising: a) at least one of a mono-, di-, or tri-acyl lipid and/or a tocopherol; b) optionally at least one phospholipid; c) at least one biocompatible, organic solvent; and d) at least one prostacyclin analogue or a salt thereof; wherein the pre-formulation forms, or is capable of forming, at least one liquid crystalline phase structure upon contact with excess aqueous fluid. Such compositions may additionally comprise polar co-solvents. Methods of treatment, particularly for management of pulmonary artery hypertension (PAH), severe PAH, Raynard's disease ischemia and related conditions are provided, as well as corresponding uses of the compositions. Administration devices comprising the formulations and kits comprising the devices are also provided.
priorityDate 2016-09-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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