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continuation (darbepoetinum)

Anemia Working Group Romania · FDA-approved active Small molecule

continuation (darbepoetinum) is a Erythropoiesis-stimulating agent (ESA) Small molecule drug developed by Anemia Working Group Romania. It is currently FDA-approved for Anemia associated with chronic kidney disease, Anemia in patients with non-myeloid malignancies receiving chemotherapy. Also known as: Darbepo Group.

Darbepoetin alfa is an erythropoiesis-stimulating agent that binds to the erythropoietin receptor to stimulate red blood cell production.

Darbepoetin alfa is an erythropoiesis-stimulating agent that binds to the erythropoietin receptor to stimulate red blood cell production. Used for Anemia associated with chronic kidney disease, Anemia in patients with non-myeloid malignancies receiving chemotherapy.

At a glance

Generic namecontinuation (darbepoetinum)
Also known asDarbepo Group
SponsorAnemia Working Group Romania
Drug classErythropoiesis-stimulating agent (ESA)
TargetErythropoietin receptor (EPOR)
ModalitySmall molecule
Therapeutic areaHematology
PhaseFDA-approved

Mechanism of action

Darbepoetin alfa is a recombinant human erythropoietin analog engineered with two additional N-linked carbohydrate chains, which extends its half-life compared to epoetin alfa. It activates the erythropoietin receptor on erythroid progenitor cells in the bone marrow, promoting their proliferation, differentiation, and maturation into mature red blood cells. This mechanism increases hemoglobin levels and reduces the need for blood transfusions in anemic patients.

Approved indications

Common side effects

Key clinical trials

Primary sources

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

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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Frequently asked questions about continuation (darbepoetinum)

What is continuation (darbepoetinum)?

continuation (darbepoetinum) is a Erythropoiesis-stimulating agent (ESA) drug developed by Anemia Working Group Romania, indicated for Anemia associated with chronic kidney disease, Anemia in patients with non-myeloid malignancies receiving chemotherapy.

How does continuation (darbepoetinum) work?

Darbepoetin alfa is an erythropoiesis-stimulating agent that binds to the erythropoietin receptor to stimulate red blood cell production.

What is continuation (darbepoetinum) used for?

continuation (darbepoetinum) is indicated for Anemia associated with chronic kidney disease, Anemia in patients with non-myeloid malignancies receiving chemotherapy.

Who makes continuation (darbepoetinum)?

continuation (darbepoetinum) is developed and marketed by Anemia Working Group Romania (see full Anemia Working Group Romania pipeline at /company/anemia-working-group-romania).

Is continuation (darbepoetinum) also known as anything else?

continuation (darbepoetinum) is also known as Darbepo Group.

What drug class is continuation (darbepoetinum) in?

continuation (darbepoetinum) belongs to the Erythropoiesis-stimulating agent (ESA) class. See all Erythropoiesis-stimulating agent (ESA) drugs at /class/erythropoiesis-stimulating-agent-esa.

What development phase is continuation (darbepoetinum) in?

continuation (darbepoetinum) is FDA-approved (marketed).

What are the side effects of continuation (darbepoetinum)?

Common side effects of continuation (darbepoetinum) include Hypertension, Thrombovascular events, Headache, Injection site pain, Flu-like symptoms.

What does continuation (darbepoetinum) target?

continuation (darbepoetinum) targets Erythropoietin receptor (EPOR) and is a Erythropoiesis-stimulating agent (ESA).

Related

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