http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2131651-A1

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filingDate 2008-03-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_07d409bf38e84f748d26dbcfa70d86f1
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publicationDate 2009-12-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2131651-A1
titleOfInvention Topical corneal analgesia using neurotensin receptor agonists and synergistic neurotensin combinations without delaying wound healing
abstract A method for administering an ocular analgesic is described. The method includes the steps of providing a topical analgesic that includes a neo-tryptophan-containing neurotensin analog and applying the topical analgesic to the ocular tissue in a dose of about 0.0005 to about 1.2 mg, alternatively about 0.0005 to about 1.0 mg, alternatively about 0.00075 to about 1.0 mg, alternatively about 0.001 mg to about 1.0 mg, alternatively about 0.001 mg to about 0.8 mg, alternatively about 0.001 mg to about 0.7 mg, alternatively about 0.001 mg to about 0.6 mg. Methods of administering a topical analgesic containing a neo-tryptophan-containing neurotensin analog are also described. The topical analgesic can be administered in a patch, gel, lotion, spray, or mist.
priorityDate 2007-03-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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