Treatment of relapsed and/or refractory solid tumors and non-Hodgkin's lymphomas
Methods are provided for the treatment of relapsed and/or refractory solid tumors (including neuroendocrine carcinomas (NEC)) and non-Hodgkin's lymphomas (NHLs) and the like, using substituted heterocyclic derivative compounds and pharmaceutical compositions comprising compounds useful for the inhibition of lysine specific demethylase-1 (LSD-1).
1. A method for the treatment of human merkel cell carcinoma comprising administration to a patient in need thereof an effective amount of a compound having the structure of:
or a pharmaceutically acceptable salt thereof.
2. The method of claim 1 , wherein the administration is oral administration.
3. The method of claim 1 , wherein the effective amount of the compound comprises about 1.5 mg/kg to about 10 mg/kg.
4. The method of claim 1 , wherein the compound is combined with at least one pharmaceutically acceptable excipient.
5. The method of claim 1 , wherein the compound is in the form of a tablet, pill, sachet, or capsule of hard or soft gelatin.
6. The method of claim 5 , wherein the compound is in the form of a tablet.
7. The method of claim 5 , wherein the compound is in the form of a pill.
8. The method of claim 5 , wherein the compound is in the form of a sachet.
9. The method of claim 5 , wherein the compound is in the form of a hard gelatin capsule.
10. The method of claim 5 , wherein the compound is in the form of a soft gelatin capsule.
11. The method of claim 1 , wherein the compound is in the form of a capsule comprising the compound at dosage strengths of about 0.50 mg, about 0.75 mg, or about 2.00 mg.
12. The method of claim 11 , wherein the compound is in the form of a capsule comprising the compound at a dosage strength of about 0.50 mg.
13. The method of claim 11 , wherein the compound is in the form of a capsule comprising the compound at a dosage strength of about 0.75 mg.
14. The method of claim 11 , wherein the compound is in the form of a capsule comprising the compound at a dosage strength of about 2.00 mg.