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In one embodiment the invention is defined by the combined weight percentage of hygroscopic and freely soluble diluents in the dosage form, and the weight ratio of hygroscopic diluent to freely soluble diluent.

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Incorporation of a heavy atom particularly substitution of deuterium for hydrogen, can give rise to an isotope effect that can alter the pharmacokinetics of the drug.

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In particular, the invention relates to the use of excipients that promote the bioavailability of such formulations, including alkaline buffering agents, gas forming excipients, hygroscopic excipients, water soluble diluents, wetting agents, and particular pharmaceutically acceptable salts.

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In yet another embodiment, the DMD is a DMOAD selected from the group consisting of glucosamine, chondroitin sulfate, calcitonin, alendronate, risedronate, zoledronic acid, teriparatide, VX-765, pralnacasan, SB-462795, CPA-926, ONO-4817, S 3536, PG-530742, CP-544439 and pharmaceutically acceptable salts thereof.

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In certain cases, discontinuation of therapy may be necessary.

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