Compositions and methods of using modified release solabegron for lower urinary tract symptoms
This application relates to pharmaceutical compositions, comprising solabegron that are useful for the treatment of lower urinary tract symptoms such as, for example, overactive bladder and prostate disorders. Additionally, this application relates to methods for treating lower urinary tract symptoms utilizing the pharmaceutical compositions, comprising solabegron. In some embodiments, the pharmaceutical compositions, comprising solabegron comprise a dual release drug delivery system.
1. A pharmaceutical composition comprising:
an immediate release composition comprising about 75 mg of solabegron and at least one pharmaceutically acceptable carrier, and
a delayed release composition comprising about 200 mg of solabegron and at least one pharmaceutically acceptable carrier, and
wherein the pharmaceutical composition achieves a first plasma C max of about 0.5 μg/ml to about 4 μg/ml in about 0.75 hours to about 4 hours after administration, a second plasma C max of about 0.5 μg/ml to about 4 μg/ml in about 6 hours to about 16 hours after administration, a first plasma C min of about 0.25 mg/ml to about 1.5 mg/ml between the first plasma C max and the second plasma C max in about 4 hours to about 8 hours after administration, a second plasma C min of about 0.01 mg/ml to about 1 mg/ml before about 24 hours after administration, and wherein the second plasma C min is achieved after the second plasma C max , and
wherein the pharmaceutical composition reduces desensitization of a beta-3 adrenoceptor when compared to an immediate release pharmaceutical composition comprising an equivalent amount of solabegron administered twice daily, and
wherein the pharmaceutical composition is a solid.
2. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition is a tablet, a bi-layer tablet, a capsule, a multiparticulate, a drug coated sphere, a matrix tablet, or a multicore tablet.
3. The pharmaceutical composition of claim 1 , wherein the immediate release composition is coated on a core comprising the delayed release composition.
4. The pharmaceutical composition of claim 2 , wherein the multiparticulate composition comprises a first population of immediate release solabegron pellets and a second population of delayed release solabegron pellets, and the first population of pellets is configured to release solabegron in upper GI tract, and the second population of pellets is configured to release solabegron in lower GI tract.
5. The pharmaceutical composition of claim 1 , wherein the solabegron is an amorphous solid form of solabegron.
6. The pharmaceutical composition of claim 1 , wherein the solabegron is a crystalline solid form of solabegron.
7. The pharmaceutical composition of claim 1 , wherein the solabegron is a pharmaceutically acceptable salt of solabegron.
8. The pharmaceutical composition of claim 1 , further comprising one more additional therapeutic agents selected from the groups consisting of antimuscarinic agents, alpha adrenoceptor blockers, botulinum toxin, purinergics, cannabinoids, transient receptor potential (TRP) protein inhibitors, prostaglandins, percutaneous tibial nerve stimulation, 5-alpha reductase inhibitors, phosphodiesterase-5 inhibitors, and combination thereof.
9. A pharmaceutical composition comprising:
an immediate release composition comprising about 125 mg of solabegron and at least one pharmaceutically acceptable carrier, and
a delayed release composition comprising about 275 mg of solabegron and at least one pharmaceutically acceptable carrier, and
wherein the pharmaceutical composition achieves a first plasma C max of about 0.5 μg/ml to about 4 μg/ml in about 0.75 hours to about 4 hours after administration, a second plasma C max of about 0.5 μg/ml to about 4 μg/ml in about 6 hours to about 16 hours after administration, a first plasma C min of about 0.25 mg/ml to about 1.5 mg/ml between the first plasma C max and the second plasma C max in about 4 hours to about 8 hours after administration, a second plasma C min of about 0.01 mg/ml to about 1 mg/ml before about 24 hours after administration, and wherein the second plasma C min is achieved after the second plasma C max , and
wherein the pharmaceutical composition reduces desensitization of a beta-3 adrenoceptor when compared to an immediate release pharmaceutical composition comprising an equivalent amount of solabegron administered twice daily, and
wherein the pharmaceutical composition is a solid.
10. The pharmaceutical composition of claim 9 , wherein the pharmaceutical composition is a tablet, a bi-layer tablet, a capsule, a multiparticulate, a drug coated sphere, a matrix tablet, or a multicore tablet.
11. The pharmaceutical composition of claim 9 , wherein the immediate release composition is coated on a core comprising the delayed release composition.
12. The pharmaceutical composition of claim 10 , wherein the multiparticulate composition comprises a first population of immediate release solabegron pellets and a second population of delayed release solabegron pellets, and the first population of pellets is configured to release solabegron in upper GI tract, and the second population of pellets is configured to release solabegron in lower GI tract.
13. The pharmaceutical composition of claim 9 , wherein the solabegron is an amorphous solid form of solabegron.
14. The pharmaceutical composition of claim 9 , wherein the solabegron is a crystalline solid form of solabegron.
15. The pharmaceutical composition of claim 9 , wherein the solabegron is a pharmaceutically acceptable salt of solabegron.
16. The pharmaceutical composition of claim 9 , further comprising one more additional therapeutic agents selected from the groups consisting of antimuscarinic agents, alpha adrenoceptor blockers, botulinum toxin, purinergics, cannabinoids, transient receptor potential (TRP) protein inhibitors, prostaglandins, percutaneous tibial nerve stimulation, 5-alpha reductase inhibitors, phosphodiesterase-5 inhibitors, and combination thereof.