ArticleAnnals of medicine and surgery (2012)2025
Nipocalimab: a significant milestone in the treatment of myasthenia gravis approved by the FDA.
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 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Structure and function of therapeutic antibodies approved by the US FDA in 2025.Antibody therapeutics · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Nipocalimab is a newly approved therapeutic agent that modulates a distinct immune transport pathway and has shown considerable promise in treating patients with motor impairment stemming from dysregulated antibody responses. Cleared for use in individuals aged 12 and older, this biology marks a notable advancement in managing many autoimmune conditions, including myasthenia gravis which exists in 150-200 individuals per million. The results of nipocalimab in patients with the latter condition were read in peer-reviewed literature and clinical trial data and key outcomes were extracted. The disease in focus is characterized by fluctuating muscular weakness and reduced endurance due to immune system disruption at the neuromuscular interface. While existing interventions offer some relief, many are limited by side effects or suboptimal long-term control, underscoring the need for better-targeted therapies. Interrupting the mechanism that prolongs the circulation of specific immune proteins presents a refined strategy to lower pathogenic activity while maintaining overall immunological integrity. This compound disrupts the cellular routing system involved in antibody preservation, leading to a selective decline in disease-associated immunoglobulins while leaving protective antibodies largely unaffected. Clinical studies across healthy and affected populations have demonstrated a favorable safety record and meaningful biological responses, including enhanced physical functioning. Late-stage trials have confirmed significant improvements in key health parameters, reinforcing the agent's therapeutic value. This biology introduces a more precise, well-tolerated, and durable option for treating myasthenia gravis.
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Registered trials
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 Socratic graph.