Pembrolizumab
Phase 2Recruiting 1 views this week 0 watching⚡ Active
Interest: 42/100
42
Development Stage
✓
Pre-clinical✓
Phase 13
Phase 24
Phase 35
ApprovedIndication / Disease
Cutaneous Squamous Cell Carcinoma of the Head and Neck
Conditions
Cutaneous Squamous Cell Carcinoma of the Head and Neck, Head and Neck Cancer
Trial Timeline
Jun 28, 2022 → Jun 1, 2027
NCT ID
NCT05025813About Pembrolizumab
Pembrolizumab is a phase 2 stage product being developed by Merck for Cutaneous Squamous Cell Carcinoma of the Head and Neck. The current trial status is recruiting. This product is registered under clinical trial identifier NCT05025813. Target conditions include Cutaneous Squamous Cell Carcinoma of the Head and Neck, Head and Neck Cancer.
What happened to similar drugs?
7 of 20 similar drugs in Cutaneous Squamous Cell Carcinoma of the Head and Neck were approved
Approved (7) Terminated (1) Active (12)
Hype Score Breakdown
Clinical
12
Activity
15
Company
15
Novelty
0
Community
0
Clinical Trials (20)
| NCT ID | Phase | Status |
|---|---|---|
| NCT02083484 | Pre-clinical | Completed |
| NCT07302347 | Phase 1/2 | Recruiting |
| NCT07089992 | Phase 2 | Recruiting |
| NCT07007273 | Phase 2 | Recruiting |
| NCT04569461 | Phase 2 | Withdrawn |
| NCT05815927 | Phase 3 | Recruiting |
| NCT05852223 | Phase 2 | Recruiting |
| NCT05879120 | Phase 2 | Withdrawn |
| NCT06004336 | Phase 2 | Recruiting |
| NCT05496036 | Phase 2 | Recruiting |
| NCT05131919 | Phase 2 | Active |
| NCT05197322 | Phase 2 | Recruiting |
| NCT05406713 | Phase 2 | Active |
| NCT05025813 | Phase 2 | Recruiting |
| NCT06413095 | Phase 1 | Completed |
| NCT05191472 | Phase 2 | Terminated |
| NCT05204160 | Phase 2 | Withdrawn |
| NCT04575961 | Phase 2 | Active |
| NCT04417166 | Phase 2 | Recruiting |
| NCT05188508 | Phase 2 | Recruiting |
Competing Products
20 competing products in Cutaneous Squamous Cell Carcinoma of the Head and Neck
| Product | Company | Stage | Hype Score |
|---|---|---|---|
| ONTAK (denileukin difitox, DAB389IL-2) | Eisai | Approved | 43 |
| ONTAK | Eisai | Approved | 43 |
| E7777 9 mcg/kg | Eisai | Phase 3 | 40 |
| ONTAK | Eisai | Approved | 43 |
| Mogamulizumab | Kyowa Kirin | Approved | 47 |
| Mogamulizumab + Brentuximab vedotin | Kyowa Kirin | Phase 1 | 36 |
| Mogamulizumab | Kyowa Kirin | Phase 2 | 39 |
| KW-0761 + Vorinostat | Kyowa Kirin | Phase 3 | 40 |
| Enzastaurin | Eli Lilly | Phase 2 | 35 |
| Clopidogrel + Ticagrelor | AstraZeneca | Approved | 43 |
| Pembrolizumab | Merck | Phase 2 | 42 |
| Comparator: vorinostat | Merck | Pre-clinical | 26 |
| Pembrolizumab | Merck | Phase 2 | 39 |
| TR701 FA | Merck | Phase 2 | 35 |
| MK0683, vorinostat, Suberoylanilide Hydroxamic Acid (SAHA) / Duration of Treatment 6 Months | Merck | Phase 2 | 35 |
| Tulisokibart + Placebo | Merck | Phase 2 | 39 |
| Aspirin + Ipilimumab + Pembrolizumab | Merck | Phase 2 | 35 |
| Pembrolizumab + Mogamulizumab | Merck | Phase 2 | 42 |
| TR-701 FA + Linezolid | Merck | Phase 3 | 40 |
| Pimasertib + Dacarbazine | Merck | Phase 2 | 35 |