Company profile

Science 37

One Site. Any Patient. Total Access.

Clinical Trials & Research

Company profile

About Science 37

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.

Primary marketClinical Trials & Research
Commercial modelCommercial information available on request
Company presenceLinkedIn
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01 · Operating footprint

Where the Company operates

Company-profile context for clinical focus, customers, deployment, integration, milestones, and partnerships.

Clinical focus

  • Asthma
  • Bipolar Depression
  • Cardiovascular
  • Central Nervous System
  • Cholestatic Pruritus
  • Colorectal Cancer
  • COVID-19
  • Dermatology
  • Endocrinology
  • Fragile X Syndrome
  • Gastroenterology
  • Hematology
  • Immunology
  • Infectious Disease
  • Major Depressive Disorder
  • Men's Health
  • Musculoskeletal
  • Narcolepsy
  • Oncology
  • Ophthalmology
  • Parkinson's Disease
  • Postpartum Depression
  • Primary Biliary Cholangitis
  • Primary Sclerosing Cholangitis
  • Respiratory
  • Tay-Sachs & Sandhoff Disease
  • Urology
  • Vascular Ehlers-Danlos Syndrome
  • Women's Health

Who it serves

  • Biotechnology sponsors
  • Clinical trial sponsors
  • Pharma

Deployment & integration

Hybrid deployment with recorded integration context.

Geographic context

MarketsNationwide U.S. coverage · United States (all 50 states)
Company sourceOfficial website

Company milestones

Platform expansion

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

Recorded partners

  • Acer Therapeutics
  • Adrenas
  • Advarra
  • Anthos Therapeutics
  • Avillion
  • Bayer
  • Biohaven
  • Boehringer Ingelheim
  • Catalent
  • Chugai Pharmaceutical
  • Delfi
  • Escient Pharmaceuticals
  • Fuze Health
  • GSK
  • Harmony Biosciences
  • Jazz Pharmaceuticals
  • LabConnect
  • Mirum Pharmaceuticals
  • PatientsLikeMe
  • PureTech Health
  • RxE2
  • Tufts Center for the Study of Drug Development (Tufts CSDD)

02 · Flagship portfolio

Products, workflows, and platform capabilities

Selected source-backed Company products and the available commercial context.

Direct-to-Patient Site

FDA-inspected clinical research site delivering trials directly to patients' homes nationwide

Service · HybridCompany source

Pediatric Research

Dedicated pediatrics department expanding access to specialized clinical research for children

Service · HybridCompany source

Research-Grade Nursing

Specialized nursing services for in-home clinical trial visits and patient support

Service · HybridCompany source

03 · Research intelligence

Research Intelligence evidence

Publications, preprints, clinical validation, and regulatory records in Evidence Position order.

04 · Company-reported outcomes

Outcomes and case studies

Company-reported outcomes and customer stories are distinct from linked Research Intelligence evidence.

86% completion rate

Average patient completion rate across trials

20-30% of total study enrollment

Average contribution as a single site

47% of total U.S. participants

Primary Biliary Cholangitis Phase 3 trial

28% of total study participants

Asthma Phase 3 trial

49% of total study participants

Colorectal Cancer prevention trial

55% of total study participants

Narcolepsy Phase 4 trial

77% of total enrollment

Parkinson's Disease Phase 2 trial

98% retention rate

Parkinson's Disease and Narcolepsy trials

11x faster enrollment

Compared to 141 traditional sites in PBC trial

22x greater enrollment velocity

Compared to traditional sites in Asthma trial

Asthma Phase 3 Trial Sponsor

Phase 3 respiratory trial for asthma

28% of total enrollment; 44 patients per month (22x greater than traditional sites averaging 2 patients/month)

Cholestatic Pruritus Phase 2 Trial Sponsor

Phase 2 rare hepatology and gastroenterology trial

21% of total study participants; top enrolling site globally in multinational trial

Colorectal Cancer Prevention Trial Sponsor

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

COVID-19 Prophylaxis Phase 3 Trial Sponsor

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

Fragile X Syndrome Phase 3 Trial Sponsor

Phase 3 rare disease trial including pediatric patients

25% of all randomized patients nationwide; 94% patient retention rate

GSK

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

Narcolepsy Phase 3 Trial Sponsor

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

Parkinson's Disease Phase 2 Trial Sponsor

Double-blind, placebo-controlled Parkinson's disease study

77% of total enrollment; 46 participants vs 14 across 4 traditional sites; 98% retention rate

Primary Biliary Cholangitis Phase 3 Trial Sponsor

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

Vascular Ehlers-Danlos Syndrome Phase 3 Trial Sponsor

Phase 3 rare cardiology trial for vEDS

100% of total participants enrolled as single site across 19 U.S. states

05 · Leadership

Leadership team

Leadership profiles and professional links from the current Company record.

No active leadership profiles are currently listed.

06 · Company updates

Updates from Science 37

Recent articles published on Science 37's official website.

07 · HAIC coverage

Coverage and analysis

Health AI Central reporting that mentions this Company.

No HAIC coverage is currently linked to this Company.

08 · Official presence

Company sources and channels

Curated official destinations from the active Company record.

09 · Market pathway

Additional Companies in this Market

Other active Companies in the same market, selected alphabetically from the HAIC directory.

Market context

Clinical Trials & Research

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.

Explore the full market directory or compare this Company with additional active profiles.

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10 · Pro research

Coming soon

Expanded Company research is in development.

Health AI Central Pro · Coming Soon

Deeper Company research is coming soon.

Pro Research will introduce expanded technical context, linked evidence analysis, and comparative Company research.

ResearchEvidence analysis

Linked research, clinical, and regulatory source pathways.

CompanyTechnical context

Expanded product, deployment, integration, and partnership research.

MethodSource & review record

Record-level provenance and review context.

Coming Soon