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Idarubicin(IDA)

Chinese Academy of Medical Sciences · FDA-approved active Small molecule

Idarubicin(IDA) is a Anthracycline topoisomerase II inhibitor Small molecule drug developed by Chinese Academy of Medical Sciences. It is currently FDA-approved for Acute myeloid leukemia (AML), Acute lymphoblastic leukemia (ALL), Chronic myeloid leukemia in blast crisis. Also known as: darubicin, IDA, Demethoxydaunor Ubicin.

Idarubicin is a topoisomerase II inhibitor that intercalates into DNA and prevents DNA unwinding, leading to cell death in rapidly dividing cancer cells.

Idarubicin is a topoisomerase II inhibitor that intercalates into DNA and prevents DNA unwinding, leading to cell death in rapidly dividing cancer cells. Used for Acute myeloid leukemia (AML), Acute lymphoblastic leukemia (ALL), Chronic myeloid leukemia in blast crisis.

At a glance

Generic nameIdarubicin(IDA)
Also known asdarubicin, IDA, Demethoxydaunor Ubicin
SponsorChinese Academy of Medical Sciences
Drug classAnthracycline topoisomerase II inhibitor
TargetTopoisomerase II; DNA
ModalitySmall molecule
Therapeutic areaOncology
PhaseFDA-approved

Mechanism of action

Idarubicin is an anthracycline chemotherapy agent that intercalates between DNA base pairs and inhibits topoisomerase II, an enzyme essential for DNA replication and transcription. This dual mechanism causes DNA strand breaks and prevents cancer cell proliferation, ultimately triggering apoptosis. It is particularly effective against hematologic malignancies due to its ability to penetrate leukemic cells.

Approved indications

Common side effects

Key clinical trials

Primary sources

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

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Frequently asked questions about Idarubicin(IDA)

What is Idarubicin(IDA)?

Idarubicin(IDA) is a Anthracycline topoisomerase II inhibitor drug developed by Chinese Academy of Medical Sciences, indicated for Acute myeloid leukemia (AML), Acute lymphoblastic leukemia (ALL), Chronic myeloid leukemia in blast crisis.

How does Idarubicin(IDA) work?

Idarubicin is a topoisomerase II inhibitor that intercalates into DNA and prevents DNA unwinding, leading to cell death in rapidly dividing cancer cells.

What is Idarubicin(IDA) used for?

Idarubicin(IDA) is indicated for Acute myeloid leukemia (AML), Acute lymphoblastic leukemia (ALL), Chronic myeloid leukemia in blast crisis.

Who makes Idarubicin(IDA)?

Idarubicin(IDA) is developed and marketed by Chinese Academy of Medical Sciences (see full Chinese Academy of Medical Sciences pipeline at /company/chinese-academy-of-medical-sciences).

Is Idarubicin(IDA) also known as anything else?

Idarubicin(IDA) is also known as darubicin, IDA, Demethoxydaunor Ubicin.

What drug class is Idarubicin(IDA) in?

Idarubicin(IDA) belongs to the Anthracycline topoisomerase II inhibitor class. See all Anthracycline topoisomerase II inhibitor drugs at /class/anthracycline-topoisomerase-ii-inhibitor.

What development phase is Idarubicin(IDA) in?

Idarubicin(IDA) is FDA-approved (marketed).

What are the side effects of Idarubicin(IDA)?

Common side effects of Idarubicin(IDA) include Myelosuppression (neutropenia, thrombocytopenia, anemia), Cardiotoxicity (dose-dependent), Mucositis, Nausea and vomiting, Alopecia, Hepatotoxicity.

What does Idarubicin(IDA) target?

Idarubicin(IDA) targets Topoisomerase II; DNA and is a Anthracycline topoisomerase II inhibitor.

Related

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