Alendronate (Fosamax)
Pre-clinicalCompleted 1 views this week 0 watching💤 Quiet
Interest: 26/100
26
Development Stage
1
Pre-clinical2
Phase 13
Phase 24
Phase 35
ApprovedIndication / Disease
Juvenile Osteoporosis
Conditions
Juvenile Osteoporosis, Low Bone Density, Fractures
Trial Timeline
Jul 1, 2009 → Oct 1, 2010
NCT ID
NCT00920075About Alendronate (Fosamax)
Alendronate (Fosamax) is a pre-clinical stage product being developed by Merck for Juvenile Osteoporosis. The current trial status is completed. This product is registered under clinical trial identifier NCT00920075. Target conditions include Juvenile Osteoporosis, Low Bone Density, Fractures.
What happened to similar drugs?
7 of 20 similar drugs in Juvenile Osteoporosis were approved
Approved (7) Terminated (1) Active (13)
Hype Score Breakdown
Clinical
3
Activity
8
Company
15
Novelty
0
Community
0
Clinical Trials (1)
| NCT ID | Phase | Status |
|---|---|---|
| NCT00920075 | Pre-clinical | Completed |
Competing Products
20 competing products in Juvenile Osteoporosis
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| PLX-200 + Placebo | Polaryx Therapeutics | Phase 3 | 37 |
| MRA(Tocilizumab) | Chugai Pharmaceutical | Phase 3 | 40 |
| MRA(Tocilizumab) + placebo | Chugai Pharmaceutical | Phase 3 | 40 |
| MRA(Tocilizumab) | Chugai Pharmaceutical | Phase 3 | 40 |
| MRA(Tocilizumab) | Chugai Pharmaceutical | Phase 3 | 40 |
| Adalimumab | Eisai | Phase 3 | 40 |
| Abatacept | Ono Pharmaceutical | Phase 3 | 40 |
| Ixekizumab + Adalimumab | Eli Lilly | Phase 3 | 44 |
| Baricitinib + Placebo | Eli Lilly | Phase 3 | 40 |
| Baricitinib | Eli Lilly | Phase 3 | 47 |
| Baricitinib + Tocilizumab | Eli Lilly | Phase 3 | 47 |
| adalimumab + Methotrexate | AbbVie | Pre-clinical | 26 |
| Upadacitinib | AbbVie | Phase 1 | 33 |
| Upadacitinib + Tocilizumab | AbbVie | Phase 3 | 47 |
| Adalimumab + Risankizumab | AbbVie | Phase 3 | 47 |
| Adalimumab | AbbVie | Phase 3 | 40 |
| naproxen + esomeprazole | AstraZeneca | Phase 1 | 29 |
| canakinumab | Novartis | Phase 3 | 40 |
| Secukinumab | Novartis | Phase 1 | 36 |
| ACZ885 150 mg (Canakinumab) | Novartis | Phase 3 | 40 |