Direct-to-Patient Site
FDA-inspected clinical research site delivering trials directly to patients' homes nationwide
Company profile
One Site. Any Patient. Total Access.
Company profile
Science 37 is a modern clinical research site that delivers clinical trials directly to patients' homes, operating as the first and only FDA-inspected direct-to-patient site in the industry. Founded more than a decade ago by investigators with the vision to make clinical research accessible to anyone, anywhere, anytime, the company has supported over 200 clinical trials across Phases I–IV and observational studies. Science 37 operates under a single Form FDA 1572 and a central IRB, supported by centralized medical oversight, research-grade nursing, and specialized direct-to-patient clinical operations. With medical licensure across all 50 states, the company's Direct-to-Patient Site enables sponsors to expand access, improve retention, and enroll more representative patient populations compared to traditional site-based approaches. The company has successfully completed multiple FDA inspections across five Phase 3 studies, achieving No Action Indicated (NAI) classifications with zero Form 483 observations. Science 37's model consistently delivers strong performance, including approximately 86% completion rates and contributing an average of 20–30% of total study enrollment as a single site. These outcomes have been validated by the Tufts Center for the Study of Drug Development (Tufts CSDD). The company serves pharmaceutical and biotechnology sponsors, helping them accelerate clinical development by connecting patients with research opportunities earlier and making participation more accessible through traditional, hybrid, and decentralized trial models.
Company description Science 37 official website
Mission. Science 37 was founded more than a decade ago by investigators with the vision to make clinical research accessible to anyone, anywhere, anytime, regardless of their proximity to research sites.
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01 · Operating footprint
Company-profile context for clinical focus, customers, deployment, integration, milestones, and partnerships.
Hybrid deployment with recorded integration context.
Company milestones
Partnership with PatientsLikeMe announced July 2026. Published landmark peer-reviewed study with Tufts CSDD on direct-to-patient clinical trial site performance. Launched dedicated Pediatrics Department. Appointed Kelly Johnston McKee as VP of Strategy & Transformation. Supported over 200 clinical trials across Phases I-IV.
Partnerships
02 · Flagship portfolio
Selected source-backed Company products and the available commercial context.
FDA-inspected clinical research site delivering trials directly to patients' homes nationwide
Dedicated pediatrics department expanding access to specialized clinical research for children
Specialized nursing services for in-home clinical trial visits and patient support
03 · Research intelligence
Publications, preprints, clinical validation, and regulatory records in Evidence Position order.
Publications, clinical validation, and regulatory records connected to this Company appear here.
Research
International journal of environmental research and public health · Jun 5, 2026
Ruxolitinib cream monotherapy for facial and/or neck atopic dermatitis: results from a decentralized, randomized phase 2 clinical trial.The Journal of dermatological treatment · Dec 1, 2025
Safety and efficacy of pegtibatinase enzyme replacement therapy in adults with classical homocystinuria in the COMPOSE phase 1/2 randomized trial.Genetics in medicine : official journal of the American College of Medical Genetics · Aug 1, 2025
Safety of BI 1358894 in patients with major depressive disorder: Results and learnings from a phase II randomized decentralized clinical trial.Clinical and translational science · Dec 1, 2024
Targeted therapies in advanced biliary malignancies: a clinical review.Expert review of anticancer therapy · Sep 1, 2024
A Protocol for the Inclusion of Minoritized Persons in Alzheimer Disease Research From the ADNI3 Diversity Taskforce.JAMA network open · Aug 1, 2024
Clinical validation
No linked records are currently available.
Regulatory
No linked records are currently available.
04 · Company-reported outcomes
Company-reported outcomes and customer stories are distinct from linked Research Intelligence evidence.
Average patient completion rate across trials
Average contribution as a single site
Primary Biliary Cholangitis Phase 3 trial
Asthma Phase 3 trial
Colorectal Cancer prevention trial
Narcolepsy Phase 4 trial
Parkinson's Disease Phase 2 trial
Parkinson's Disease and Narcolepsy trials
Compared to 141 traditional sites in PBC trial
Compared to traditional sites in Asthma trial
Phase 3 respiratory trial for asthma
28% of total enrollment; 44 patients per month (22x greater than traditional sites averaging 2 patients/month)
Phase 2 rare hepatology and gastroenterology trial
21% of total study participants; top enrolling site globally in multinational trial
Oncology prevention trial across 49 states
49% of total study enrollment; 12,000+ participants (exceeded 7,000 goal); 24% minority representation; accelerated timeline by 3+ years
Phase 3 infectious disease study for immunocompromised cohort
42% of total participants across 36 states in 8 weeks; >90% visit completion rate across 700+ in-home visits; 23% minority representation
Phase 3 rare disease trial including pediatric patients
25% of all randomized patients nationwide; 94% patient retention rate
Making trials accessible for patients in rural areas
Enabled trial participation for patients in rural areas who would typically travel hundreds of miles to nearest clinical site
Phase 3 neurology trial for narcolepsy
55% of total study participants; 33 patients enrolled vs <1 per traditional site; 98% visit completion rate; 77% of required completers for interim analysis
Double-blind, placebo-controlled Parkinson's disease study
77% of total enrollment; 46 participants vs 14 across 4 traditional sites; 98% retention rate
Enrolling patients for Phase 3 hepatology trial
47% of total U.S. study participants enrolled; 11x faster enrollment than 141 traditional sites; 82% retention rate
Phase 3 rare cardiology trial for vEDS
100% of total participants enrolled as single site across 19 U.S. states
05 · Leadership
Leadership profiles and professional links from the current Company record.
No active leadership profiles are currently listed.
06 · Company updates
Recent articles published on Science 37's official website.
07 · HAIC coverage
Health AI Central reporting that mentions this Company.
No HAIC coverage is currently linked to this Company.
08 · Official presence
Curated official destinations from the active Company record.
09 · Market pathway
Other active Companies in the same market, selected alphabetically from the HAIC directory.
Market context
Companies using AI to optimize clinical trial design, accelerate patient recruitment, match patients to trials, predict trial outcomes, or improve clinical research efficiency. Includes patient enrollment and screening platforms, AI-powered trial matching, and tools that reduce the time and cost of bringing new treatments to market.
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Linked research, clinical, and regulatory source pathways.
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Record-level provenance and review context.