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US GLP-1 Clinical Trials & FDA Safety Monitor

Monitor semaglutide, tirzepatide, and liraglutide across ClinicalTrials.gov, FDA drug labels, NDCs, and recalls. Track obesity and type 2 diabetes trials, pipeline changes, recruiting status, safety updates, and official source links with private history and CSV reports.

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US Clinical Trials & FDA Drug Safety Monitor
US Clinical Trials & FDA Drug Safety Monitorfascinating_lentil/clinical-trials-drug-data-aggregator
Source
Query
Record Type
Record ID
+30 fields
Text
Number
Boolean
List
Object

Input

Sources:clinical_trials+2
Trial status filter:all
Trial phase filter:all
Maximum records:60
Trial conditions:obesity+1
Drug names:semaglutide+2
Locations per trial:25
Track changes across scheduled runs:true
Watchlist name:us-glp1-trials-fda-safety
Observations retained per record:24

Output fields

Source
Query
Record Type
Record ID
Change Status
Severity
Signals
Observations
Title / Name
Status
Phase
Study Type
Conditions
Generic Name
Brand Name
Sponsor / Manufacturer
Enrollment
Enrollment Change
Locations
Recruiting Locations
Recruiting Location Change
Countries
Start Date
Primary Completion
Completion Date
Last Updated
Posted Results
Results First Posted
PubMed Links
Recall Date
Classification
Adverse Event Count
Source URL
Scraped At

How it works

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The US Clinical Trials & FDA Drug Safety Monitor Actor is ready to run with the inputs already set for "US GLP-1 Clinical Trials & FDA Safety Monitor". Sign up or log in and you'll land in Apify Console with a copy of this exact task.

Start the "US GLP-1 Clinical Trials & FDA Safety Monitor" task

The US Clinical Trials & FDA Drug Safety Monitor Actor will start running based on the input automatically. You can also change all the input fields, like sources, trial status filter, and more, to match your specific use case.

Receive the "US GLP-1 Clinical Trials & FDA Safety Monitor" output

Monitor the progress in real time. You will be notified as soon as your dataset is complete and ready for review. Each result includes data such as source, query, record type, and more.

Integrate into your workflow

The final output is delivered in JSON, CSV, or Excel format, ready to be plugged into your workflow. You can also run the "US GLP-1 Clinical Trials & FDA Safety Monitor" task via API.

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