BiotechTube

raloxifene + placebo

ApprovedCompleted
1 views this week 0 watching⚡ Active
Interest: 43/100
43
Hype Score

Development Stage

✓
Pre-clinical
✓
Phase 1
✓
Phase 2
✓
Phase 3
5
Approved
Indication / Disease

Osteoporosis

Conditions

Osteoporosis

Trial Timeline

Sep 1, 2006 → Feb 1, 2010

NCT ID
NCT00371956

About raloxifene + placebo

raloxifene + placebo is a approved stage product being developed by Eli Lilly for Osteoporosis. The current trial status is completed. This product is registered under clinical trial identifier NCT00371956. Target conditions include Osteoporosis.

What happened to similar drugs?

20 of 20 similar drugs in Osteoporosis were approved

Approved (20) Terminated (0) Active (0)
✅raloxifene + PlaceboEli LillyApproved
✅MENATETRANONEEisaiApproved
✅Menatetrenone (Vitamin K2)EisaiApproved
✅teriparatideEli LillyApproved
✅Teriparatide + Aspara-CA 600 mg + Alfarol 1.0 µgEli LillyApproved
✅Teriparatide + Strontium ranelateEli LillyApproved
✅Teriparatide + Zoledronic AcidEli LillyApproved

Hype Score Breakdown

Clinical
20
Activity
8
Company
15
Novelty
0
Community
0

Clinical Trials (3)

NCT IDPhaseStatus
NCT00371956ApprovedCompleted
NCT00532246ApprovedCompleted
NCT00190593Phase 3Completed

Competing Products

20 competing products in Osteoporosis

See all competitors
ProductCompanyStageHype Score
ENZ215 + ProliaAlkem LaboratoriesPhase 3
40
Teriparatide + Alendronate Sodium + Placebo + PlaceboEli LillyPhase 3
40
TeriparatideEli LillyPhase 3
40
teriparatide + teriparatide + Placebo + Calcium Supplement + Vitamin D SupplementEli LillyPhase 3
40
raloxifene + PlaceboEli LillyApproved
43
Subcutaneous Teriparatide + Transdermal TeriparatideEli LillyPhase 2
35
teriparatide 20 micrograms/day subcutaneous + calcitonin 100 IU/day subcutaneousEli LillyPhase 3
40
Teriparatide + Salmon CalcitoninEli LillyPhase 3
40
ForteoEli LillyPre-clinical
22
arzoxifene + PlaceboEli LillyPhase 2
35
teriparatide 20 micrograms/day subcutaneous + salmon calcitonin 100 IU/day subcutaneousEli LillyPhase 3
40
CT-P41 + US-licensed ProliaCelltrionPhase 3
40
ED-71 + Alfacalcidol + ED-71 placebo + Alfacalcidol placeboChugai PharmaceuticalPhase 3
40
Eldecalcitol soft capsulesChugai PharmaceuticalPre-clinical
22
ibandronic acid 0.5mg + RIS placebo + 1.0mg ibandronic acid + ibandronic acid placebo + 2.5mg RISChugai PharmaceuticalPhase 3
40
Denosumab + Placebo + Alendronate sodium hydrateDaiichi SankyoPhase 3
40
YM529 / ONO-5920Astellas PharmaPhase 2/3
38
ONO-5920Astellas PharmaPhase 3
40
Minodronic acid hydrateAstellas PharmaPhase 3
40
ONO-5920 / YM529Astellas PharmaPhase 1
29