Vote for the Right to Trial & FDA Upgrade Act
With 95% of diseases lacking FDA-approved treatments and patients enduring 17 years of suffering, it's time for change. Help us open-source FDA.gov!
Should patients be allowed to join clinical trials for promising new treatments?
How it Works For Research Partners
Create a Trial
Upload protocols, pre/post-clinical data, and register your supply chain through the FDA.gov V2's intuitive interface.
- Simple protocol builder with templates
- Automated regulatory compliance checks
- Secure data storage and management
Get Liability Insurance
Automatically receive and select liability insurance quotes per subject with transparent pricing.
- Competitive quotes from multiple providers
- Risk-based pricing tailored to your trial
- One-click policy activation
Set Parameters
Define patient pricing, required data collection, and refundable deposits to optimize your trial.
- Flexible pricing models for participants
- Customizable data collection requirements
- Incentive structures to maximize retention
Manage Supply Chain & Orders
Track inventory, fulfill patient orders, and manage the entire treatment supply chain with end-to-end visibility.
- Automated inventory tracking and alerts
- Secure patient order processing and fulfillment
- Temperature-controlled shipping monitoring
- Blockchain-verified chain of custody
Analyze Trial Data
Access real-time insights, analyze effectiveness data, and make informed decisions with comprehensive dashboards and reporting tools.
- Real-time effectiveness monitoring
- Participant compliance tracking
- Advanced statistical analysis tools
- Regulatory submission preparation
Should patients be allowed to join clinical trials for promising new treatments?
How it Works For Patients
Find the Most Promising Treatment for Your Condition
Search for trials based on your condition, location, and preferences.
- Access trials from anywhere in the world
- Filter by condition, treatment type, and more
- See real-time availability and enrollment status
- Compare multiple treatment options side-by-side
View Outcome Labels
Review comprehensive outcome data before deciding to join a trial.
- See real effectiveness data from actual patients
- Understand potential side effects and their frequency
- Compare with standard of care treatments
- Read about experiences from patients like you
Join a Trial
Complete informed consent and enroll in your chosen trial.
- Simple digital enrollment process
- Clear explanation of trial requirements
- Transparent compensation information
- Easy withdrawal option if needed
Coordinate Your Care
Schedule lab tests, provider visits, and import your health records.
- Book appointments with just a few clicks
- Import data from your existing health records
- Attend virtual check-ins from anywhere
- Receive reminders for upcoming appointments
Track Your Data
Record your diet, treatment adherence, symptoms, and more.
- Simple mobile app for daily tracking
- Automatic data collection from wearables
- Customized tracking based on your trial
- Secure and private data storage
Gain Personal Insights
View personalized analytics about your health and treatment response.
- See how your response compares to others
- Identify patterns in your symptoms and triggers
- Track your progress over time
- Receive personalized recommendations
Connect with Your FDAi AI Agent
Receive personalized daily check-ins from your FDAi AI agent that monitors your progress, collects data, and provides insights in a conversational way.
- Daily check-ins via phone or text to monitor your well-being
- Natural conversation interface for easy data collection
- Personalized insights based on your treatment response
- Immediate alerts for potential side effects or concerns
- Medication reminders and adherence support
FDAi Agent
Your personal health assistant
Good morning, Sarah! How are you feeling today after your treatment yesterday?
I'm feeling better today. The headache is gone but I still feel a bit tired.
That's good progress! Your fatigue has decreased by 40% since last week. Would you like to see how your symptoms compare to others in your trial?
Yes, please show me.
Should patients be allowed to join clinical trials for promising new treatments?
Why We Desperately Need to Upgrade the FDA
The current medical research and approval system is demonstrably failing humanity. These statistics paint a clear, grim picture of the crisis, underscoring the urgent need for a decentralized, open, and patient-centric dFDA.
80X Potential Acceleration
In medical progress via an upgraded, decentralized FDA.gov.
$41,000 Cost Per Participant
The staggering expense in traditional clinical trials.
$1.6 Billion Development Cost
For a new treatment, a burden often falling on patients.
21K-120K Preventable Deaths
Per decade, due to sheer inefficiency in regulatory processes.
85% of Patients Excluded
From participating in vital clinical trials, denying them hope and data.
95% of Diseases Untreated
Lacking any FDA-approved treatments, leaving millions in despair.
17 Years of Suffering
The average, agonizing wait from treatment discovery to patient access.
166 Billion Untested Treatments
The vast ocean of potential cures left unexplored due to a broken system.
2 Billion People Suffering
Globally, from diseases that remain uncured, a silent pandemic.
44+ Years Since Last Disease Cure
Highlighting the profound stagnation in eradicating major diseases.
Should patients be allowed to join clinical trials for promising new treatments?
Comparative Effectiveness Rankings
Explore evidence-based rankings of interventions for various conditions
Interventions by Condition
Ranked by effectiveness based on clinical trials and real-world evidence
Metformin
Effectiveness
Based on 245 trials with 35,000 participants
GLP-1 Receptor Agonists
Effectiveness
Based on 178 trials with 28,000 participants
SGLT2 Inhibitors
Effectiveness
Based on 156 trials with 24,000 participants
DPP-4 Inhibitors
Effectiveness
Based on 189 trials with 30,000 participants
Sulfonylureas
Effectiveness
Based on 210 trials with 32,000 participants
Should patients be allowed to join clinical trials for promising new treatments?
Outcome Labels
FDA.gov v2 can provide standardized 'Outcome Labels' for all treatments, offering clear, quantitative data on benefits and risks. This transparency empowers patients and doctors to make informed decisions, especially when considering participation in clinical trials under a 'Right to Trial' framework.
- Comprehensive health impact data
- Both positive and negative effects
- Evidence-based decision making
Source information not available.
Vote on The Right to Trial & FDA Upgrade Act
Do you support the following proposals?