Concizumab
Inherited Blood Coagulation Disorder
Explore 3 assets in Inherited Blood Coagulation Disorder →Floatz Rating
BB64/100
Confidence
Indicative
Sponsor
Novo Nordisk A/S
Modality
monoclonal_antibody
Development Phase
Phase 2
Status
Dormant
Evidence ledger · v0.2
Clinical Evidence
Clinical track record: trial progression, reported outcomes, safety signals, and endpoint quality.
49High confidence
Detailed axis rationale is planned and will be published soon.
| Trial | Phase | Status | N | Primary endpoint | Readout |
|---|---|---|---|---|---|
NCT03196284CT.gov A Trial Evaluating the Efficacy and Safety of Prophylactic Administration of Concizumab in Haemophilia A and B Patients With Inhibitors | — | Completed | — | — | — |
NCT02490787CT.gov Trial Investigating Safety, Pharmacokinetics and Pharmacodynamics of Concizumab Administered Subcutaneously to Haemophilia A Subjects | — | Completed | — | — | — |
Competitive Position
Competitive setting: how crowded the indication is, class-level failures, and timing against rivals.
95High confidence
Detailed axis rationale is planned and will be published soon.
Same indication · Inherited Blood Coagulation Disorder
| Asset | Sponsor | Phase | Rating |
|---|---|---|---|
| Concizumab (this asset) | Novo Nordisk A/S | P2 | BB · 64 |
| Turoctocog Alfa | Novo Nordisk A/S | P4 | A |
| Eptacog Alfa (Activated) | Novo Nordisk A/S | P4 | A |
| Nonacog Beta Pegol | Novo Nordisk A/S | P3 | A |
| N8-GP | Novo Nordisk A/S | P3 | A |
| Human Antihemophilic Factor/Von Willebrand Factor Complex | Assiut University | P4 | BB |
| Feiba | Novo Nordisk A/S | P4 | BB |
| Factor Ix | Novo Nordisk A/S | P4 | BB |
| Vatreptacog Alfa (Activated) | Novo Nordisk A/S | P3 | BB |
+9 more in the Inherited Blood Coagulation Disorder cohort
Other indications for Concizumab
| Indication | Sponsor | Phase | Rating |
|---|---|---|---|
| Hemophilia A | — | P3 | BB · 68 |
| Hemophilia B | — | P3 | BB · 66 |
| Hemophilia | — | P3 | B · 60 |
Scientific Foundation
Strength of the underlying biology: target validation, tractability, modality fit, and how related mechanisms have fared.
NR
Planned for methodology v0.2.
Development Feasibility
How realistically the program can be executed, drawing on modality precedent, enrollment dynamics, and sponsor delivery.
NR
Planned for methodology v0.2.
Commercial Opportunity
Commercial prize: addressable population, unmet need, and the value case for the indication.
NR
Planned for methodology v0.2.
IP & Exclusivity
Exclusivity position, covering patent protection and freedom-to-operate runway.
NR
Planned for methodology v0.2.
Manufacturing & Supply
Manufacturing and supply readiness, driven by modality process and scale-up risk.
NR
Planned for methodology v0.2.
Related assets
Citation
Floatz Terminal. Concizumab in Inherited Blood Coagulation Disorder. Methodology v0.2. Rated under v0.2 effective July 8, 2026. Last refreshed July 8, 2026. Accessed July 14, 2026. https://terminal.floatz.ai/assets/concizumab-inherited-blood-coagulation-disorder
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