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HLD200

Ironshore Pharmaceuticals and Development, Inc · Phase 3 active Small molecule

HLD200 is a histone deacetylase (HDAC) inhibitor that modulates gene expression by blocking HDAC enzymes.

HLD200 is a histone deacetylase (HDAC) inhibitor that modulates gene expression by blocking HDAC enzymes. Used for Peripheral T-cell lymphoma (PTCL).

At a glance

Generic nameHLD200
Also known asmethylphenidate hydrochloride (MPH)
SponsorIronshore Pharmaceuticals and Development, Inc
Drug classHDAC inhibitor
TargetHistone deacetylase (HDAC)
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

By inhibiting histone deacetylase activity, HLD200 prevents the removal of acetyl groups from histone proteins, leading to increased histone acetylation and altered chromatin structure. This results in changes to gene expression patterns, particularly affecting genes involved in cell proliferation and differentiation. The drug is being developed for hematologic malignancies where HDAC inhibition has shown therapeutic potential.

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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