Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Drug Discovery: Overview01:26

Drug Discovery: Overview

Drug discovery is a multifaceted process involving extensive screening, testing, and optimization of lead compounds to identify potential new drugs for therapeutic use. It combines several approaches, including screening large numbers of natural products, chemical modification of known active molecules, identification of new drug targets, and rational design based on biological mechanisms and drug-receptor structure. These approaches are carried out in both academic research laboratories and...
Bioequivalence of Drugs: Drugs with Multiple Indications01:09

Bioequivalence of Drugs: Drugs with Multiple Indications

The concept of therapeutic equivalence (TE) in drugs with multiple indications is complex. A generic drug may be therapeutically equivalent to a brand-name product for one specific indication, but this doesn't necessarily mean it's equivalent for all other indications. Evidence of TE in one patient group and bioequivalence shown in healthy volunteers can support—but not confirm—TE for other indications. However, definitive proof requires individual clinical studies for each indication due to...
Drug Nomenclature01:17

Drug Nomenclature

During the development of a new pharmaceutical, the manufacturer initially assigns a code name to the drug. Once approved, the drug receives a United States Adopted Name (USAN)—a generic, nonproprietary designation. Upon being listed in the United States Pharmacopeia, this nonproprietary name becomes the drug's official name. Additionally, the manufacturer assigns a proprietary name or trademark, which serves as the brand name under which the drug is marketed. It is worth noting that the same...
Targets for Drug Action: Overview01:26

Targets for Drug Action: Overview

Drugs target macromolecules to modify ongoing cellular processes. Primary drug targets include receptors, ion channels, transporters, and enzymes.
Receptors are either membrane-spanning or intracellular proteins, which upon binding a ligand, get activated and transmit the signal downstream to elicit a response. Drugs bind receptors, either mimicking the action of endogenous ligands or blocking the receptor activity to bring about a modified response. Nearly 35% of approved drugs target the G...
Pharmacogenomics: Identification of New Drug Targets01:29

Pharmacogenomics: Identification of New Drug Targets

Advances in genomics have profoundly influenced drug discovery by increasing both the speed and accuracy of pharmaceutical development. Pharmacogenomics, which examines how genetic variation influences drug response, facilitates the identification of novel therapeutic targets and enables patient stratification for personalized treatment. These strategies contribute to improved drug efficacy, minimized adverse effects, and more efficient clinical trial design.Mapping genetic differences...
Structure-Activity Relationships and Drug Design01:28

Structure-Activity Relationships and Drug Design

Drug design is a dynamic field that involves discovering and developing new medications based on specific biological targets. This process heavily relies on structure-activity relationships (SAR) and quantitative structure-activity relationships (QSAR) to guide the design and optimization of efficient drugs.
SAR studies the intricate relationship between a drug's chemical structure and biological activity. It focuses on understanding how modifications to a drug's structure can influence its...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Establishing a health information exchange research network (HIERN) to support population health studies.

NPJ digital medicine·2026
Same author

THERA-IE: An AI-Enabled System for Therapeutic Indication Identification and Extraction from Biomedical Literature.

Studies in health technology and informatics·2026
Same author

From Food to Clinic: Mapping FoodOn to the UMLS to Enable Nutritional Decision Support.

AMIA ... Annual Symposium proceedings. AMIA Symposium·2026
Same author

Building a collaborative ecosystem across the IDeA-CTR networks in response to a public health emergency.

Journal of clinical and translational science·2025
Same author

Barriers and facilitators to COVID-19 testing and vaccination: a qualitative focus group study among Rhode Island's Latine/Hispanic community.

Frontiers in health services·2025
Same author

"<i>They fell through the cracks:</i>" caregiver perspectives on the difficulties of COVID-19 implementation transitions for children and youth with special healthcare needs (CYSHCN).

Frontiers in pediatrics·2025
Same journal

LabSage: Structural-Semantic Decoupling for Enhanced Retrieval-Augmented Generation in Clinical Laboratories.

AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science·2026
Same journal

Evaluating Representation Embeddings from LLMs and Time-Series Foundation Models for Wearable Accelerometer-Based Health Prediction.

AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science·2026
Same journal

ClinNoteAgents: An LLM Multi-Agent System for Predicting and Interpreting Heart Failure 30-Day Readmission from Clinical Notes.

AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science·2026
Same journal

Mapping the Storm: Linking Tornado Paths to Emergency Room Surges Through Geocoded Patient Data.

AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science·2026
Same journal

Multi-Modal Deep Learning-Based Model to Predict Burkitt Lymphoma Recurrence.

AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science·2026
Same journal

A Multi-Model LLM Consensus Framework to Identify EHR-Predictable Eligibility Criteria in NSCLC Immunotherapy Trials.

AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science·2026
See all related articles

Related Experiment Video

Updated: Jun 20, 2026

Drug Repurposing Hypothesis Generation Using the "RE:fine Drugs" System
05:10

Drug Repurposing Hypothesis Generation Using the "RE:fine Drugs" System

Published on: December 11, 2016

Evaluating NLP Approaches to Extract Drug Indications.

Indra Neil Sarkar1

  • 1Center for Biomedical Informatics, Brown University, Providence, RI.

AMIA Joint Summits on Translational Science Proceedings. AMIA Joint Summits on Translational Science
|June 19, 2026
PubMed
Summary
This summary is machine-generated.

General-purpose large language models (LLMs) show promise for extracting drug indications from FDA labels, outperforming specialized models. Gemma2 achieved the best results, highlighting LLMs

Related Experiment Videos

Last Updated: Jun 20, 2026

Drug Repurposing Hypothesis Generation Using the "RE:fine Drugs" System
05:10

Drug Repurposing Hypothesis Generation Using the "RE:fine Drugs" System

Published on: December 11, 2016

Area of Science:

  • Natural Language Processing (NLP)
  • Pharmacovigilance
  • Biomedical Informatics

Background:

  • Extracting reliable drug-indication knowledge is crucial for clinical decision support and pharmacovigilance.
  • Manual curation of drug indications is labor-intensive and difficult to scale, necessitating automated approaches.
  • FDA Structured Product Labels are a key source for drug indication information.

Purpose of the Study:

  • To evaluate and benchmark nine NLP approaches for extracting therapeutic indications from FDA Structured Product Labels.
  • To compare the performance of general-purpose and biomedical-specialized large language models (LLMs) against traditional methods.
  • To establish a performance benchmark for LLM-based indication extraction.

Main Methods:

  • Evaluated nine NLP approaches: dictionary-based matching (QuickUMLS), a biomedical-pretrained transformer (PubMedBERT), and seven LLMs.
  • Benchmarked against 1,838 manually curated indication statements for twenty common medications.
  • Assessed performance using metrics including F1-Score, analyzing variations by drug indication complexity.

Main Results:

  • General-purpose LLMs outperformed biomedical-specialized LLMs and dictionary-based methods.
  • Gemma2 (2B parameters) achieved the highest F1-Score (0.568), demonstrating strong performance despite its size.
  • Dictionary-based matching (QuickUMLS) resulted in a low F1-Score (0.106) due to excessive false positives.
  • Extraction accuracy varied significantly by drug, with narrow indications performing better than broad or symptom-adjacent ones.

Conclusions:

  • General-purpose LLMs represent a viable and high-performing approach for automated drug-indication extraction.
  • Biomedical-specific LLMs did not outperform general-purpose models in this task.
  • Hybrid NLP pipelines combining LLMs with precision-oriented validation may offer optimal performance for indication extraction.