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Obizur (SUSOCTOCOG ALFA)

Baxalta Innovations GmbH · FDA-approved approved Recombinant protein Under review Quality 13/100

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 nameSUSOCTOCOG ALFA
SponsorBaxalta Innovations GmbH
ModalityRecombinant protein
Therapeutic areaHematology
PhaseFDA-approved
First approval2015

Approved indications

Common side effects

No common side effects on file.

Key clinical trials

Patents

PatentExpiryType
Biologic Exclusivity

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results
FDA Orange BookPatents + exclusivity

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Frequently asked questions about Obizur

What is Obizur?

Obizur (SUSOCTOCOG ALFA) is a Recombinant protein drug developed by Baxalta Innovations GmbH, indicated for Acquired factor VIII deficiency disease.

What is Obizur used for?

Obizur is indicated for Acquired factor VIII deficiency disease.

Who makes Obizur?

Obizur is developed and marketed by Baxalta Innovations GmbH (see full Baxalta Innovations GmbH pipeline at /company/baxalta-innovations-gmbh).

What is the generic name of Obizur?

SUSOCTOCOG ALFA is the generic (nonproprietary) name of Obizur.

When was Obizur approved?

Obizur was first approved on 2015.

What development phase is Obizur in?

Obizur is FDA-approved (marketed).

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing