ABSTRACT OF DISCLOSURE The invention relates to a process for preparing the (20S) 3.alpha .- [(aminoacetyl) amino] 5a-pregnan-20-ol and its addition salts with organic acids or pharmaceu-tically acceptable mineral that consists essentially of subjecting the funtumidine to the action of an amino acid: , Then to cleave the group R and, where appropriate, salifying the product so obtained. The (20S) 3.alpha .- [(aminoacetyl) amino] 5.alpha.-pregnan-20-ol and its addition salts with organic or inorganic acids in particular stimulate the defenses of the organism in particular potentiating the production of immunoglobulin E.
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