Hutchinson-Gilford progeria syndrome

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At a Glance

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Regulatory Watchboard

3 events
Mar 2026Integrating Peritoneal Histological Growth Patterns Into Preoperative Decision-Making for Colorectal Peritoneal Metastses

Jules Bordet Institute

TrialNOT YET RECRUITING
Jan 2025Study to Determine Optimal Dose and Evaluate Safety, Tolerability, and Pharmacokinetics of Progerinin in Patients With Hutchinson-Gilford Progeria Syndrome (HGPS)

PRG Science & Technology Co., Ltd. — PHASE2

TrialACTIVE NOT RECRUITING
Nov 2020Zokinvy: FDA approved

in patients 12 months of age and older with a body surface area (BSA) of 0.39 m2 and above (1) to reduce the risk of mortality in Hutchinson-Gilford Progeria Syndrome (HGPS); and (2) for the treatment of processing-deficient Progeroid Laminopathies with either heterozygous LMNA mutation with progerin-like protein accumulation or homozygous or compound heterozygous ZMPSTE24 mutations

FDAcompleted

Data from FDA regulatory filings and ClinicalTrials.gov. Updated periodically.

Financial Assistance

1 program

FINANCIAL LANDSCAPE SUMMARY

1

Total programs

1

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Patient Assistance Programs1

Zokinvy

Sentynl Therapeutics, Inc.

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Approved Treatments

1 FDA-approved

Zokinvy

(LONAFARNIB)Orphan drug

Sentynl Therapeutics, Inc.

Farnesyltransferase Inhibitor [EPC]

12.1 Mechanism of Action Lonafarnib inhibits farnesyltransferase to prevent farnesylation and subsequent accumulation of progerin and progerin-like pr...

Approved Nov 2020FDA label ↗

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Clinical Trial Landscape

1 active trial
1Phase 2
1Total recruiting
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Recent News & Research

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Specialist Network

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