Cytogam
ApprovedRecruiting 0 watching 0 views this week๐ Rising
77
Development Stage
โ
Pre-clinicalโ
Phase 1โ
Phase 2โ
Phase 35
ApprovedIndication / Disease
Cytomegalovirus (CMV) Infection
Conditions
Cytomegalovirus (CMV) Infection
Trial Timeline
Jun 26, 2025 โ Dec 1, 2027
NCT ID
NCT07009548About Cytogam
Cytogam is a approved stage product being developed by Kamada for Cytomegalovirus (CMV) Infection. The current trial status is recruiting. This product is registered under clinical trial identifier NCT07009548. Target conditions include Cytomegalovirus (CMV) Infection.
Hype Score Breakdown
Clinical
30
Activity
20
Company
2
Novelty
10
Community
12
Clinical Trials (1)
| NCT ID | Phase | Status |
|---|---|---|
| NCT07009548 | Approved | Recruiting |
Competing Products
20 competing products in Cytomegalovirus (CMV) Infection
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| ASP0113 + Placebo | Astellas Pharma | Phase 2 | 52 |
| ASP0113 + Placebo | Astellas Pharma | Phase 3 | 77 |
| Letermovir oral granules + Letermovir tablet + Letermovir intravenous | Merck | Phase 2 | 52 |
| Letermovir 240 mg Oral Tablet | Merck | Phase 2 | 52 |
| Letermovir tablet + Letermovir IV | Merck | Phase 3 | 77 |
| Letermovir | Merck | Phase 1 | 33 |
| Letermovir | Merck | Approved | 85 |
| Letermovir 480 MG [Prevymis] | Merck | Phase 2 | 52 |
| V160 Low Dose IM + V160 Medium Dose IM + V160 High Dose IM + V160 Medium Dose plus Merck Aluminum Phosphate Adjuvant (MAPA) 225 ยตg /dose IM + V160 High Dose plus MAPA 225 ยตg /dose IM + V160 Maximum Dose IM + V160 Medium Dose ID | Merck | Phase 1 | 33 |
| Ganciclovir | Merck | Pre-clinical | 23 |
| Letermovir + Placebo | Merck | Phase 3 | 77 |
| Letermovir | Merck | Phase 2 | 52 |
| V160 + Placebo | Merck | Phase 2 | 52 |
| V160 | Merck | Phase 1 | 33 |
| Letermovir | Merck | Phase 3 | 77 |
| Letermovir | Merck | Phase 3 | 77 |
| Valganciclovir + Ganciclovir | Roche | Phase 3 | 77 |
| Zidovudine + Didanosine + Ganciclovir | Roche | Phase 1 | 33 |
| Valganciclovir | Roche | Pre-clinical | 23 |
| Foscarnet sodium + Ganciclovir | Roche | Phase 1 | 33 |