Tegaserod
Phase 2Completed 0 watching 0 views this week⚡ Active
52
Development Stage
✓
Pre-clinical✓
Phase 13
Phase 24
Phase 35
ApprovedIndication / Disease
Symptomatic Gastroespohageal Reflux Disease
Conditions
Symptomatic Gastroespohageal Reflux Disease
Trial Timeline
Jan 1, 2004 → Jun 1, 2005
NCT ID
NCT00149851About Tegaserod
Tegaserod is a phase 2 stage product being developed by Novartis for Symptomatic Gastroespohageal Reflux Disease. The current trial status is completed. This product is registered under clinical trial identifier NCT00149851. Target conditions include Symptomatic Gastroespohageal Reflux Disease.
Hype Score Breakdown
Clinical
17
Activity
12
Company
10
Novelty
5
Community
5
Clinical Trials (20)
| NCT ID | Phase | Status |
|---|---|---|
| NCT00511771 | Pre-clinical | Completed |
| NCT00414024 | Phase 3 | Terminated |
| NCT00390975 | Approved | Terminated |
| NCT00399659 | Phase 3 | Terminated |
| NCT00365820 | Phase 2/3 | Terminated |
| NCT00348634 | Approved | Terminated |
| NCT00171457 | Phase 3 | Completed |
| NCT00171470 | Phase 3 | Completed |
| NCT00139568 | Phase 3 | Completed |
| NCT00563758 | Pre-clinical | Terminated |
| NCT00563615 | Pre-clinical | UNKNOWN |
| NCT00171431 | Phase 3 | Terminated |
| NCT00232037 | Phase 3 | Completed |
| NCT00232102 | Phase 3 | Completed |
| NCT00232089 | Phase 3 | Completed |
| NCT00142974 | Phase 2 | Terminated |
| NCT00142987 | Approved | Completed |
| NCT00149877 | Approved | Completed |
| NCT00141089 | Phase 3 | Completed |
| NCT00171483 | Phase 3 | Completed |
Competing Products
20 competing products in Symptomatic Gastroespohageal Reflux Disease
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| Sodium hyaluronate + placebo injection | Daiichi Sankyo | Phase 3 | 77 |
| ISV-305 | Sun Pharmaceutical | Phase 3 | 77 |
| rabeprazole sodium + Placebo | Eisai | Phase 3 | 77 |
| Verinurad + Febuxostat + Dapagliflozin | AstraZeneca | Phase 2 | 52 |
| RDEA3170 + Febuxostat + Benzbromarone | AstraZeneca | Phase 1/2 | 41 |
| Esomeprazole + Matching placebo | AstraZeneca | Phase 3 | 77 |
| DFV890 + Placebo | Novartis | Phase 2 | 52 |
| Omalizumab + Omalizumab + Placebo | Novartis | Phase 2 | 52 |
| Pasireotide + Octreotide | Novartis | Phase 3 | 77 |
| valsartan | Novartis | Approved | 85 |
| Atorvastatin - Cholestyramine - Sitosterol | Pfizer | Pre-clinical | 22 |
| Epoetin biosimilar | Pfizer | Pre-clinical | 22 |
| Apixaban + Standard of care | Pfizer | Phase 3 | 76 |
| Azithromycin plus chloroquine | Pfizer | Phase 3 | 76 |
| Mavacamten | Bristol Myers Squibb | Approved | 84 |
| Aficamten + Placebo | Sanofi | Phase 3 | 76 |
| Vandetanib 300 mg | Sanofi | Pre-clinical | 22 |
| REGN7508 + Acetylsalicylic Acid (ASA) + Placebo | Regeneron Pharmaceuticals | Phase 3 | 76 |
| Rivaroxaban + Placebo | Bayer | Phase 3 | 74 |
| Droxidopa capsules + Placebo capsules | Lundbeck | Approved | 82 |