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Paraplatin (Carboplatin)

MYLAN SEIYAKU Ltd · FDA-approved approved Small molecule Quality 62/100

Carboplatin produces predominantly interstrand DNA cross-links in a cell-cycle nonspecific manner.

Carboplatin is indicated for initial treatment of advanced ovarian carcinoma in combination with other chemotherapeutic agents and for palliative treatment of recurrent ovarian carcinoma after prior chemotherapy. It demonstrates equivalent efficacy to cisplatin with a more favorable aquation profile, though patients with progressive disease during prior cisplatin therapy may have decreased response rates. The drug exhibits linear pharmacokinetics with biphasic plasma decay and primarily renal elimination. Carboplatin is contraindicated in patients with severe allergic reactions to platinum compounds, severe bone marrow depression, or significant bleeding.

At a glance

Generic nameCarboplatin
SponsorMYLAN SEIYAKU Ltd
Drug classPlatinum-containing alkylating agent
TargetDNA
ModalitySmall molecule
Therapeutic areaOncology
PhaseFDA-approved
First approval1989

Mechanism of action

Carboplatin, like cisplatin, produces predominantly interstrand DNA cross-links rather than DNA-protein cross-links through a cell-cycle nonspecific mechanism. The aquation of carboplatin, which produces the active species, occurs at a slower rate than cisplatin. Despite differences in aquation rates, both carboplatin and cisplatin induce equal numbers of drug-DNA cross-links, causing equivalent lesions and biological effects, with potency differences directly related to aquation rate differences.

Approved indications

Boxed warnings

Common side effects

Key clinical trials

Patents

PatentExpiryType

Primary sources

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