1 mg QD to 15 mg QD PF-06649751 + 3 mg QD to 15 mg QD PF-06649751 + 7 mg QD to 15 mg QD PF-06649751 + 15 mg QD PF-06649751 + 1 mg QD to 7 mg QD PF-06649751 (if de-escalated in parent study) + 3 mg QD to 7 mg QD PF-06649751 (de-escalated in parent study) + 7 mg QD to 7 mg QD PF-06649751 (de-escalated in parent study) + 15 mg QD de-escalated to 7 mg QD PF-06649751 in parent study remain at 7 mg QD
Phase 2TerminatedDevelopment Stage
Parkinson's Disease With Motor Fluctuations
Parkinson's Disease With Motor Fluctuations
Jul 6, 2017 → Oct 25, 2017
About 1 mg QD to 15 mg QD PF-06649751 + 3 mg QD to 15 mg QD PF-06649751 + 7 mg QD to 15 mg QD PF-06649751 + 15 mg QD PF-06649751 + 1 mg QD to 7 mg QD PF-06649751 (if de-escalated in parent study) + 3 mg QD to 7 mg QD PF-06649751 (de-escalated in parent study) + 7 mg QD to 7 mg QD PF-06649751 (de-escalated in parent study) + 15 mg QD de-escalated to 7 mg QD PF-06649751 in parent study remain at 7 mg QD
1 mg QD to 15 mg QD PF-06649751 + 3 mg QD to 15 mg QD PF-06649751 + 7 mg QD to 15 mg QD PF-06649751 + 15 mg QD PF-06649751 + 1 mg QD to 7 mg QD PF-06649751 (if de-escalated in parent study) + 3 mg QD to 7 mg QD PF-06649751 (de-escalated in parent study) + 7 mg QD to 7 mg QD PF-06649751 (de-escalated in parent study) + 15 mg QD de-escalated to 7 mg QD PF-06649751 in parent study remain at 7 mg QD is a phase 2 stage product being developed by Pfizer for Parkinson's Disease With Motor Fluctuations. The current trial status is terminated. This product is registered under clinical trial identifier NCT03185481. Target conditions include Parkinson's Disease With Motor Fluctuations.
What happened to similar drugs?
20 of 20 similar drugs in Parkinson's Disease With Motor Fluctuations were approved
Hype Score Breakdown
Clinical Trials (1)
| NCT ID | Phase | Status |
|---|---|---|
| NCT03185481 | Phase 2 | Terminated |
Competing Products
20 competing products in Parkinson's Disease With Motor Fluctuations
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| UB-312 + Placebo | Vaxxinity | Phase 1 | 19 |
| NAV5001 + DaTscan | Navidea Biopharmaceuticals | Phase 3 | 22 |
| piclozotan + 0.9% sodium chloride (normal saline) | Daiichi Sankyo | Phase 2 | 35 |
| E2007 | Eisai | Phase 3 | 32 |
| ARICEPT | Eisai | Phase 3 | 40 |
| Perampanel | Eisai | Phase 3 | 32 |
| GPI 1485 | Eisai | Phase 2 | 35 |
| E2007 | Eisai | Phase 3 | 40 |
| Prior Donepezil 5mg + Prior Donzepezil 10mg + Prior Placebo | Eisai | Phase 3 | 40 |
| perampanel + placebo | Eisai | Phase 2 | 27 |
| Lemborexant + placebo | Eisai | Approved | 50 |
| Placebo + E2007 + E2007 | Eisai | Phase 3 | 32 |
| E2007 + E2007 + E2007 | Eisai | Phase 2 | 35 |
| E2007 | Eisai | Phase 2 | 35 |
| E2007 | Eisai | Phase 2 | 27 |
| E2007 | Eisai | Phase 2 | 27 |
| 2 mg perampanel + 4 mg perampanel + placebo comparator | Eisai | Phase 3 | 40 |
| Istradefylline (KW-6002) | Kyowa Kirin | Phase 2 | 35 |
| Istradefylline 20 mg or 40 mg | Kyowa Kirin | Phase 3 | 40 |
| Istradefylline (KW-6002) | Kyowa Kirin | Phase 3 | 40 |