Organic compounds
The invention relates to particular substituted heterocycle fused gamma-carbolines, their prodrugs, in free, solid, pharmaceutically acceptable salt and/or substantially pure form as described herein, pharmaceutical compositions thereof, and methods of use in the treatment of diseases involving the 5-HT 2A receptor, the serotonin transporter (SERT), pathways involving the dopamine D 1 and D 2 receptor signaling system, and/or the μ-opioid receptor.
1. A method for the treatment of a central nervous system disorder, comprising administering to a patient in need thereof a compound of a Formula I:
wherein:
X is —NH—;
L is O;
Z is —O— or —C(O)—;
in free or salt form;
wherein the disorder is selected from the group consisting of obsessive-compulsive disorder (OCD), obsessive-compulsive personality disorder (OCPD), general anxiety disorder, social anxiety disorder, panic disorder, agoraphobia, compulsive gambling disorder, compulsive eating disorder, body dysmorphic disorder, hypochondriasis, pathological grooming disorder, kleptomania, pyromania, attention deficit-hyperactivity disorder (ADHD), attention deficit disorder (ADD), impulse control disorder, pain disorders, cephalic pain, neuropathic pain, idiopathic pain, chronic pain, fibromyalgia, chronic fatigue, opiate dependency, cocaine dependency, amphetamine dependency, alcohol dependency, and combinations thereof.
2. The method according to claim 1 , wherein the compound is:
3. The method according to claim 1 , wherein the compound is:
4. The method according to claim 1 , wherein the compound is in the form of a pharmaceutically acceptable salt.
5. The method according to claim 1 , wherein the compound is administered to the patient in the form of a pharmaceutically acceptable composition comprising the compound in free or pharmaceutically acceptable salt form, in admixture with a pharmaceutically acceptable diluent or carrier.
6. The method of claim 5 , wherein the pharmaceutically acceptable diluent or carrier comprises a polymeric matrix.
7. The method according to claim 6 , wherein the polymeric matrix is a biodegradable poly(d,l-lactide-co-glycolide) microsphere.
8. The method according to claim 1 wherein the central nervous system disorder is selected from obsessive-compulsive disorder (OCD), obsessive-compulsive personality disorder (OCPD), general anxiety disorder, social anxiety disorder, panic disorder, agoraphobia, compulsive gambling disorder, compulsive eating disorder, body dysmorphic disorder, hypochondriasis, pathological grooming disorder, kleptomania, pyromania, attention deficit-hyperactivity disorder (ADHD), attention deficit disorder (ADD) and impulse control disorder.
9. The method according to claim 8 , wherein the central nervous system disorder is obsessive-compulsive disorder (OCD) or obsessive-compulsive personality disorder (OCPD).
10. The method according to claim 1 , wherein said patient is not responsive to or cannot tolerate the side effects from treatment with selective serotonin reuptake inhibitors (SSRIs).
11. The method according to claim 10 , wherein the selective serotonin reuptake inhibitor (SSRI) is selected from the group consisting of citalopram, escitalopram, fluoxetine, fluvoxamine, paroxetine, and sertraline.
12. The method according to claim 1 , wherein said patient is not responsive to or cannot tolerate the side effects from treatment with serotonin-norepinephrine reuptake inhibitors (SNRIs).
13. The method according to claim 12 , wherein the serotonin-norepinephrine reuptake inhibitor (SNRI) is selected from the group consisting of venlafaxine, sibutramine, duloxetine, atomoxetine, desvenlafaxine, milnacipran, and levomilnacipran.
14. The method according to claim 1 , wherein said patient is not responsive to or cannot tolerate the side effects from treatment with antipsychotic agents.
15. The method according to claim 14 , wherein the antipsychotic agent is selected from the group consisting of clomipramine, risperidone, quetiapine and olanzapine.