Use of tavapadon in treating parkinson's disease
OwnerSridhar Duvvuriinventor
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Abstract
The present disclosure relates to methods for treating a patient diagnosed with Parkinson's Disease (PD) by administering an escalating dose of tavapadon and monitoring efficacy of PD treatment.
Claims42
A method for treating Parkinson's Disease in a patient, wherein the method comprises:
- a titration phase comprising orally administering to the patient a daily dose of tavapadon in eight sequential dose escalation steps 1-8, wherein
- step 2 comprises administering to the patient a dose of 0.5 mg per day of tavapadon on days 5-8 of treatment,
- step 6 comprises administering to the patient a dose of 2.25 mg per day of tavapadon on days 21-24 of treatment,
- step 8 comprises administering to the patient a dose of a therapeutically effective amount of 5 mg per day of tavapadon,
- thereby treating the Parkinson's Disease.
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A method for treating Parkinson's Disease in a patient, wherein the method comprises:
- a titration phase comprising orally administering to the patient:
- 0.25 mg per day dose of tavapadon for days 1-4 of the titration phase;
- 0.5 mg per day dose of tavapadon for days 5-8 of the titration phase;
- 0.75 mg per day dose of tavapadon for days 9-12 of the titration phase;
- 1.0 mg per day dose of tavapadon for days 13-16 of the titration phase;
- 1.5 mg per day dose of tavapadon for days 17-20 of the titration phase;
- 2.25 mg per day dose of tavapadon for days 21-24 of the titration phase;
- 3 mg per day dose of tavapadon for days 25-40 of the titration phase;
- and
- a therapeutically effective amount of 5 mg per day dose of tavapadon for days 41-56 of the titration phase;
- thereby treating the Parkinson's Disease.
A method for treating Parkinson's Disease in a patient, wherein the method comprises:
- i. a titration phase comprising orally administering to the patient:
- 0.25 mg per day dose of tavapadon for days 1-4 of the titration phase;
- 0.5 mg per day dose of tavapadon for days 5-8 of the titration phase;
- 0.75 mg per day dose of tavapadon for days 9-12 of the titration phase;
- 1.0 mg per day dose of tavapadon for days 13-16 of the titration phase;
- 1.5 mg per day dose of tavapadon for days 17-20 of the titration phase;
- 2.25 mg per day dose of tavapadon for days 21-24 of the titration phase;
- 3 mg per day dose of tavapadon for days 25-40 of the titration phase;
- and a therapeutically effective amount of 5 mg per day dose of tavapadon for days 41-56 of the titration phase;
- ii. followed by an adjustment phase comprising orally administering to the patient:
- a therapeutically effective amount of 10 mg per day dose of tavapadon, and
- a therapeutically effective amount of 15 mg per day dose of tavapadon,
- wherein the dose of tavapadon is adjusted over the range of 5, 10 or 15 mg based on patient tolerability;
- and
- iii. followed by a maintenance phase comprising orally administering to the patient:
- a therapeutically effective amount of 5, 10 or 15 mg per day dose of tavapadon;
- wherein the patient is administered the highest tolerated dose achieved during the adjustment phase and the maintenance phase maintains the patient on a steady dose of tavapadon,
- thereby treating the Parkinson's Disease.
A method for treating Parkinson's Disease in a patient, wherein the method comprises:
- i. a titration phase comprising orally administering to the patient:
- 0.25 mg per day dose of tavapadon for days 1-4 of the titration phase;
- 0.5 mg per day dose of tavapadon for days 5-8 of the titration phase;
- 0.75 mg per day dose of tavapadon for days 9-12 of the titration phase;
- 1.0 mg per day dose of tavapadon for days 13-16 of the titration phase;
- 1.5 mg per day dose of tavapadon for days 17-20 of the titration phase;
- 2.25 mg per day dose of tavapadon for days 21-24 of the titration phase;
- 3 mg per day dose of tavapadon for days 25-40 of the titration phase;
- and a therapeutically effective amount of 5 mg per day dose of tavapadon for days 41-56 of the titration phase;
- ii. followed by an adjustment phase comprising orally administering to the patient:
- a therapeutically effective amount of 10 mg per day dose of tavapadon, and
- wherein a patient who is unable to increase the dose from 5 mg to 10 mg on the first day of step 9 due to tolerability issues will begin a maintenance phase at the patient's maximum tolerated dose of 5 mg per day;
- and
- iii. followed by a maintenance phase comprising orally administering to the patient:
- a therapeutically effective amount of 5, 10 or 15 mg per day dose of tavapadon;
- wherein the patient is administered the highest tolerated dose achieved during the adjustment phase and the maintenance phase maintains the patient on a steady dose of tavapadon,
- thereby treating the Parkinson's Disease.
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Dependencies are inferred from the claim text.