tigecycline
Phase 3Completed 0 watching 0 views this week๐ Rising
76
Development Stage
โ
Pre-clinicalโ
Phase 1โ
Phase 24
Phase 35
ApprovedIndication / Disease
Gram-Negative Bacterial Infections
Conditions
Gram-Negative Bacterial Infections
Trial Timeline
Dec 1, 2003 โ Nov 1, 2005
NCT ID
NCT00079989About tigecycline
tigecycline is a phase 3 stage product being developed by Pfizer for Gram-Negative Bacterial Infections. The current trial status is completed. This product is registered under clinical trial identifier NCT00079989. Target conditions include Gram-Negative Bacterial Infections.
Hype Score Breakdown
Clinical
27
Activity
18
Company
9
Novelty
9
Community
10
Clinical Trials (18)
| NCT ID | Phase | Status |
|---|---|---|
| NCT01560143 | Approved | Completed |
| NCT01401023 | Pre-clinical | Completed |
| NCT01072539 | Pre-clinical | Completed |
| NCT00827541 | Pre-clinical | Completed |
| NCT00575094 | Phase 3 | Completed |
| NCT00419991 | Approved | Completed |
| NCT00406237 | Phase 1 | Completed |
| NCT00488488 | Pre-clinical | Completed |
| NCT00376324 | Phase 1 | Completed |
| NCT00488306 | Approved | Completed |
| NCT00488761 | Approved | Completed |
| NCT00136201 | Phase 3 | Completed |
| NCT00205816 | Phase 3 | Completed |
| NCT00079989 | Phase 3 | Completed |
| NCT00079885 | Phase 3 | Completed |
| NCT00079976 | Phase 3 | Completed |
| NCT00081744 | Phase 3 | Completed |
| NCT00600600 | Phase 2 | Completed |
Competing Products
14 competing products in Gram-Negative Bacterial Infections
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| Cefiderocol + Standard of Care | Shionogi | Phase 2 | 52 |
| Cefiderocol | Shionogi | Pre-clinical | 23 |
| Cefiderocol + Standard of Care | Shionogi | Phase 2 | 52 |
| Cefiderocol + Standard of Care | Shionogi | Phase 2 | 52 |
| HRS-8427 | Jiangsu Hengrui Medicine | Phase 1 | 33 |
| Part A: ATM-AVI Single Dose, Cohorts 1-4 + Part B: Multiple-dose ATM-AVI, Cohorts 1-4 | AbbVie | Phase 2 | 52 |
| IMI/REL + Active Control + Oral Switch | Merck | Phase 2/3 | 65 |
| IMI/REL FDC | Merck | Phase 1 | 33 |
| Ceftolozane-Tazobactam + Meropenem | Merck | Phase 3 | 77 |
| Ceftolozane/Tazobactam 1000/500 mg + Ceftolozane/Tazobactam 30/15 mg/kg + Ceftolozane/Tazobactam 20/10 mg/kg + Ceftolozane/Tazobactam 18/9 mg/kg + Ceftolozane/Tazobactam 12/6 mg/kg | Merck | Phase 1 | 33 |
| nacubactam + meropenem | Roche | Phase 1 | 33 |
| Part A: Single Dose Ceftazidime-Avibactam, Cohorts 1-3 + Part B: Multiple-dose Ceftazidime-Avibactam, Cohorts 1-3 | Pfizer | Phase 2 | 51 |
| ATM-AVI + BAT | Pfizer | Phase 2 | 51 |
| AN3365 + Placebo | Pfizer | Phase 1 | 32 |