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Obizur (SUSOCTOCOG ALFA)
Obizur (generic name: SUSOCTOCOG ALFA) is a Recombinant protein drug developed by Baxalta Innovations GmbH. It is currently FDA-approved (first approved 2015) for Acquired factor VIII deficiency disease.
Obizur is an exogenous protein used to treat hemophilia A, and it works by replacing the coagulation factor VIII. It is administered to patients with severe hemophilia A.
At a glance
| Generic name | SUSOCTOCOG ALFA |
|---|---|
| Sponsor | Baxalta Innovations GmbH |
| Modality | Recombinant protein |
| Therapeutic area | Hematology |
| Phase | FDA-approved |
| First approval | 2015 |
Approved indications
- Acquired factor VIII deficiency disease
Common side effects
Key clinical trials
Patents
| Patent | Expiry | Type |
|---|---|---|
| Biologic Exclusivity |
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| FDA label | Mechanism, indications, dosing, boxed warnings, drug interactions |
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
| FDA Orange Book | Patents + exclusivity |
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- Obizur CI brief — competitive landscape report
- Obizur updates RSS · CI watch RSS
- Baxalta Innovations GmbH portfolio CI
Frequently asked questions about Obizur
What is Obizur?
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Related
- Manufacturer: Baxalta Innovations GmbH — full pipeline
- Therapeutic area: All drugs in Hematology
- Indication: Drugs for Acquired factor VIII deficiency disease
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing