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D+Z

Sequential Medicine Ltd · FDA-approved active Small molecule

D+Z is a fixed-dose combination of daclatasvir and sofosbuvir that inhibits hepatitis C virus NS5A and NS5B proteins to block viral replication.

D+Z is a fixed-dose combination of daclatasvir and sofosbuvir that inhibits hepatitis C virus NS5A and NS5B proteins to block viral replication. Used for Chronic hepatitis C virus infection (genotype-independent).

At a glance

Generic nameD+Z
SponsorSequential Medicine Ltd
Drug classDirect-acting antiviral (DAA) combination
TargetHCV NS5A protein and HCV NS5B RNA-dependent RNA polymerase
ModalitySmall molecule
Therapeutic areaVirology / Hepatology
PhaseFDA-approved

Mechanism of action

Daclatasvir is an NS5A inhibitor that disrupts hepatitis C virus replication and assembly, while sofosbuvir is a nucleotide analog NS5B polymerase inhibitor that terminates viral RNA chain elongation. Together, they provide a direct-acting antiviral combination effective against multiple HCV genotypes without requiring ribavirin or interferon.

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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