The present application describes novel cyclic sulfonyl derivatives of formula
I:
##STR1##
or pharmaceutically acceptable salt forms thereof, wherein ring B is a 5-7 membered
cyclic system containing from 0-2 heteroatoms selected from O, N, NRa,
and S(O)p, and 0-1 carbonyl groups and the other variables are defined
in the present specification, which are useful as metalloprotease inhibitors.