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LY333334 + Placebo

Phase 1Completed
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Interest: 29/100
29
Hype Score

Development Stage

✓
Pre-clinical
2
Phase 1
3
Phase 2
4
Phase 3
5
Approved
Indication / Disease

Osteoporosis, Postmenopausal

Conditions

Osteoporosis, Postmenopausal

Trial Timeline

Nov 1, 2010 → May 1, 2011

NCT ID
NCT01250145

About LY333334 + Placebo

LY333334 + Placebo is a phase 1 stage product being developed by Eli Lilly for Osteoporosis, Postmenopausal. The current trial status is completed. This product is registered under clinical trial identifier NCT01250145. Target conditions include Osteoporosis, Postmenopausal.

What happened to similar drugs?

20 of 20 similar drugs in Osteoporosis, Postmenopausal were approved

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

Hype Score Breakdown

Clinical
6
Activity
8
Company
15
Novelty
0
Community
0

Clinical Trials (1)

NCT IDPhaseStatus
NCT01250145Phase 1Completed

Competing Products

20 competing products in Osteoporosis, Postmenopausal

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
raloxifene + placeboEli LillyApproved
43
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