Sensipar® + Vitamin D
ApprovedCompleted 0 views this week 0 watching⚡ Active
Interest: 43/100
43
Development Stage
✓
Pre-clinical✓
Phase 1✓
Phase 2✓
Phase 35
ApprovedIndication / Disease
Secondary Hyperparathyroidism
Conditions
Secondary Hyperparathyroidism
Trial Timeline
Aug 1, 2005 → Dec 1, 2006
NCT ID
NCT00135304About Sensipar® + Vitamin D
Sensipar® + Vitamin D is a approved stage product being developed by Amgen for Secondary Hyperparathyroidism. The current trial status is completed. This product is registered under clinical trial identifier NCT00135304. Target conditions include Secondary Hyperparathyroidism.
What happened to similar drugs?
6 of 20 similar drugs in Secondary Hyperparathyroidism were approved
Approved (6) Terminated (0) Active (14)
Hype Score Breakdown
Clinical
20
Activity
8
Company
15
Novelty
0
Community
0
Clinical Trials (1)
| NCT ID | Phase | Status |
|---|---|---|
| NCT00135304 | Approved | Completed |
Competing Products
20 competing products in Secondary Hyperparathyroidism
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| ASP7991 + Cinacalcet + Placebo | Astellas Pharma | Phase 2 | 35 |
| Fycompa | Eisai | Pre-clinical | 26 |
| Fycompa | Eisai | Pre-clinical | 26 |
| KHK7580 + KRN1493 | Kyowa Kirin | Phase 2/3 | 38 |
| KHK7580 | Kyowa Kirin | Phase 1 | 29 |
| KHK7580 | Kyowa Kirin | Phase 3 | 40 |
| KHK7580 | Kyowa Kirin | Phase 3 | 40 |
| Cinacalcet HCl | Kyowa Kirin | Approved | 43 |
| KHK7580 + Cinacalcet Hydrochloride | Kyowa Kirin | Phase 3 | 40 |
| Placebo + KHK7580 low dose + KHK7580 middle dose + KHK7580 high dose + KRN1493 | Kyowa Kirin | Phase 2 | 35 |
| dirucotide + Placebo | Eli Lilly | Phase 2/3 | 38 |
| dirucotide | Eli Lilly | Phase 2/3 | 30 |
| Paricalcitol + Calcitriol | AbbVie | Pre-clinical | 18 |
| paricalcitol + maxacalcitol + paricalcitol placebo + maxacalcitol placebo | AbbVie | Phase 3 | 40 |
| Paricalcitol + Calcifediol | AbbVie | Approved | 43 |
| Paricalcitol + Darbepoetin alfa | AbbVie | Approved | 43 |
| Birabresib Dose 20 mg | Merck | Phase 1 | 21 |
| Remibrutinib (blinded) + Placebo + Remibrutinib (Open label) | Novartis | Phase 3 | 47 |
| Ranibizumab | Novartis | Approved | 43 |
| BAF312 + Baseline disease modifying therapies (DMTs) + BNT162 + mRNA-1273 | Novartis | Approved | 43 |