Evidence map›Paper›PMID 41180755›Full record

ArticleAnnals of medicine and surgery (2012)2025

Olezarsen: FDA approval and clinical impact in familial chylomicronemia syndrome (FCS).

Muhammad Saad Khan, Devya Khaim Chandani, Erum Siddiqui, Maliha Khalid, Aminath Waafira

Abstract read
In one paragraph

Article in Annals of medicine and surgery (2012), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Muhammad Saad KhanDepartment of Medicine, Jinnah Sindh Medical University, Karachi, Pakistan.
Devya Khaim ChandaniDepartment of Medicine, Shaheed Mohtarma Benazir Bhutto Medical College, Karachi, Pakistan.
Erum SiddiquiDepartment of Medicine, Jinnah Sindh Medical University, Karachi, Pakistan.
Maliha KhalidDepartment of Medicine, Jinnah Sindh Medical University, Karachi, Pakistan.ORCID https://orcid.org/0009-0001-3413-2752
Aminath WaafiraDepartment of Medicine, Shaheed Mohtarma Benazir Bhutto Medical College, Karachi, Pakistan.ORCID https://orcid.org/0009-0000-3283-1982

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive disorder characterized by severe hypertriglyceridemia due to impaired lipoprotein lipase (LPL) function. Traditional treatments like dietary fat restriction and conventional lipid-lowering drugs offer limited benefit due to the underlying genetic deficiency. On December 19, 2024, the Food and Drug Administration approved olezarsen (Tryngolza), an antisense oligonucleotide targeting apolipoprotein C-III (apoC-III), for adults with FCS. By inhibiting apoC-III synthesis, olezarsen enhances LPL activity and facilitates triglyceride clearance. Phase 3 trials demonstrated a significant reduction in triglyceride levels and a marked decrease in pancreatitis episodes, establishing its therapeutic efficacy. Olezarsen is administered monthly via subcutaneous injection, with most adverse events being mild and transient, such as injection site reactions and occasional thrombocytopenia. While short-term outcomes are promising, long-term safety, cost-effectiveness, and broader accessibility remain key concerns. Furthermore, the drug exemplifies the integration of computational biology and precision medicine, laying the foundation for AI-driven innovations in managing rare lipid disorders. Overall, olezarsen represents a major advancement in FCS treatment, addressing an urgent unmet clinical need and reshaping the therapeutic landscape of ultra-rare metabolic diseases.

Indexed as

familial chylomicronemia syndromehypertriglyceridemialipoprotein lipaseolezarsenpancreatitis

Identifiers

PMID41180755
PMCPMC12577896

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.