Anwilva
Healthcare / Clinical Research
Overview
Anwvila is a powerful family tree and health mapping platform built for families affected by rare genetic conditions. Designed to bridge the gap between underserved patients and life-saving clinical trials, Anwvila enables users to track inherited disorders across generations, highlight genetic risk markers, and connect directly with relevant research studies. The app offers both a personal tool for families and a clinical resource for researchers seeking trial participants in the rare disease space.
The Challenge
Pharmaceutical companies developing treatments for rare diseases face a significant challenge: recruiting enough qualified participants for clinical trials. At the same time, many patients and families affected by these conditions lack the tools to properly document their genetic history or understand how to navigate the clinical research landscape. Traditional genealogy tools don’t account for medical complexity, and most clinical trial platforms don’t allow for family-based matching—leaving a critical gap in care and access.
Our Solution
Anwvila was built using Bubble.io as a no-code foundation, with custom logic and a specialized plugin to support rich family tree visualization and genetic tracking. Key features and solutions implemented include: - Advanced Family Tree Visualization: Custom-built functionality allows users to map family relationships across multiple generations while flagging individuals with known or suspected genetic conditions. - Genetic Marker Tagging: Users can tag family members with specific conditions, symptoms, or confirmed genetic mutations—creating a visual database of how a condition may have passed through generations. - Clinical Trial Matching: A built-in matching engine compares family data with eligibility criteria for active clinical trials, allowing families to find relevant research opportunities and enabling researchers to discover qualified participants. - Privacy & Consent Controls: The app incorporates secure sharing features, allowing families to control who sees their data and whether they want to participate in trials, research, or advocacy networks. - Custom Plugin Development: A specialized Bubble plugin was developed to support the dynamic relationships and conditional logic required for real-time, filterable family trees—something standard Bubble components couldn’t handle out of the box. We built Anwvila using Bubble.io and a custom plugin to visualize and filter complex family relationships. The app allows users to map rare conditions across generations, flag genetic markers, and connect with relevant clinical trials.
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The Results
Since its launch, Anwvila has: - Enabled families to clearly document their genetic history and better understand their health risks. - Provided a streamlined way for researchers and pharmaceutical companies to locate highly specific patient cohorts for rare disease trials—reducing recruitment time and increasing trial success rates. - Served as a unique example of how no-code tools like Bubble can be used to solve highly technical and sensitive healthcare challenges through thoughtful design and specialized plugins. Anwvila represents a major step forward in rare disease advocacy and research by giving families the tools they need to tell their stories and get access to cutting-edge treatments.
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Contact Information
michael.marsack@martech-studios.com
Phone
570-982-0108