Compositions for treating CMT and related disorders

1. A method of treating Charcot-Marie-Tooth disease or a neuropathy, comprising administering to a subject in need thereof a composition comprising an effective amount of at least baclofen, D-sorbitol and naltrexone, or pharmaceutically acceptable salts thereof, wherein baclofen, D-sorbitol and naltrexone are in a relative weight ratio of 8.6/300/1.

2. The method of claim 1 , wherein the composition further comprises a pharmaceutically suitable excipient or carrier.

3. The method of claim 1 , wherein the composition is formulated with a drug eluting polymer, a biomolecule, a micelle or liposome-forming lipids or oil in water emulsions, or pegylated or solid nanoparticles or microparticles for oral or parenteral or intrathecal administration.

4. The method of claim 1 , wherein the neuropathy is selected from idiopathic neuropathies, diabetic neuropathy, toxic neuropathies, neuropathies induced by drug treatments, neuropathies provoked by HIV, neuropathies provoked by radiation, neuropathies provoked by heavy metals, neuropathies provoked by vitamin deficiency states, or traumatic neuropathies.

5. The method of claim 4 , wherein the traumatic neuropathies arise from brain injury, spinal cord injury, or peripheral nerves injuries.

6. A method of improving nerve regeneration in a subject suffering from Charcot-Marie-Tooth disease, amyotrophic lateral sclerosis, or a neuropathy selected from an idiopathic neuropathy, diabetic neuropathy, a toxic neuropathy, a neuropathy induced by drug treatment, a neuropathy provoked by HIV, a neuropathy provoked by radiation, a neuropathy provoked by heavy metals, a neuropathy provoked by vitamin deficiency states, or a traumatic neuropathy, said method comprising administering to said subject an amount of a composition effective to improve nerve regeneration in said subject, said composition comprising baclofen, D-sorbitol and naltrexone or pharmaceutically acceptable salts thereof, wherein baclofen, D-sorbitol and naltrexone are in a relative weight ratio of 8.6/300/1.

7. The method of claim 6 , wherein the composition further comprises a pharmaceutically suitable excipient or carrier.

8. The method of claim 6 , wherein the composition is formulated with a drug eluting polymer, a biomolecule, a micelle or liposome-forming lipids or oil in water emulsions, or pegylated or solid nanoparticles or microparticles for oral or parenteral or intrathecal administration.

9. The method of claim 6 , wherein improving nerve regeneration comprises improving or accelerating recovery.

10. The method of claim 6 , wherein improving nerve regeneration comprises improving nerve myelination or restoring, at least partially, axon morphology or electrophysiological functions.

11. The method of claim 6 , wherein the traumatic neuropathy arises from brain injury, spinal cord injury, or peripheral nerves injuries.