secukinumab + placebo
Phase 2Completed 0 watching 0 views this week⚡ Active
52
Development Stage
✓
Pre-clinical✓
Phase 13
Phase 24
Phase 35
ApprovedIndication / Disease
Psoriasis, Plaque-type Psoriasis
Conditions
Psoriasis, Plaque-type Psoriasis
Trial Timeline
Jan 1, 2012 → Dec 1, 2014
NCT ID
NCT01537432About secukinumab + placebo
secukinumab + placebo is a phase 2 stage product being developed by Novartis for Psoriasis, Plaque-type Psoriasis. The current trial status is completed. This product is registered under clinical trial identifier NCT01537432. Target conditions include Psoriasis, Plaque-type Psoriasis.
Hype Score Breakdown
Clinical
17
Activity
12
Company
10
Novelty
5
Community
5
Clinical Trials (19)
| NCT ID | Phase | Status |
|---|---|---|
| NCT05722522 | Phase 3 | Terminated |
| NCT05758415 | Phase 3 | Terminated |
| NCT04737330 | Phase 3 | Terminated |
| NCT04732117 | Phase 3 | Completed |
| NCT04181762 | Phase 3 | Terminated |
| NCT04156620 | Phase 3 | Completed |
| NCT03713632 | Phase 3 | Completed |
| NCT03713619 | Phase 3 | Completed |
| NCT03055494 | Approved | Completed |
| NCT02896127 | Phase 3 | Completed |
| NCT02696031 | Phase 3 | Completed |
| NCT02599129 | Phase 2 | Terminated |
| NCT02594098 | Phase 2 | Completed |
| NCT02362789 | Phase 3 | Completed |
| NCT01989468 | Phase 3 | Completed |
| NCT02044848 | Phase 2 | Terminated |
| NCT01892436 | Phase 3 | Completed |
| NCT01807520 | Phase 3 | Completed |
| NCT01537432 | Phase 2 | Completed |
Competing Products
20 competing products in Psoriasis, Plaque-type Psoriasis
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| Ixekizumab + Placebo | Eli Lilly | Phase 2 | 52 |
| VTX958 Dose A + VTX958 Dose B + VTX958 Dose C + VTX958 Dose D + Placebo | Ventyx Biosciences | Phase 2 | 47 |
| LY2525623 Intravenous + LY2525623 Subcutaneous + Placebo Intravenous + Placebo Subcutaneous | Eli Lilly | Phase 2 | 52 |
| Ixekizumab | Eli Lilly | Phase 3 | 77 |
| 80 mg Ixekizumab Dosing Regimens 1, 2, and 3 + Placebo | Eli Lilly | Phase 3 | 77 |
| Placebo + Baricitinib | Eli Lilly | Phase 2 | 52 |
| CT-P43 + Stelara | Celltrion | Phase 3 | 77 |
| CT-P17 + EU-approved Humira | Celltrion | Phase 3 | 77 |
| CT-P55 + EU-approved Cosentyx | Celltrion | Phase 3 | 77 |
| AMG 139 | AstraZeneca | Phase 1 | 33 |
| alefacept + polyvalent pneumococcal vaccine | Astellas Pharma | Approved | 85 |
| alefacept | Astellas Pharma | Phase 2 | 52 |
| Tacrolimus Cream | Astellas Pharma | Phase 3 | 77 |
| alefacept | Astellas Pharma | Phase 3 | 77 |
| peficitinib + Placebo | Astellas Pharma | Phase 2 | 52 |
| Alefacept | Astellas Pharma | Phase 3 | 77 |
| Amevive exposure | Astellas Pharma | Pre-clinical | 23 |
| alefacept + placebo | Astellas Pharma | Phase 3 | 77 |
| alefacept | Astellas Pharma | Approved | 85 |
| ASKP1240 + Placebo | Astellas Pharma | Phase 2 | 52 |