Hekma cierra la brecha entre la atención al paciente y la investigación farmacéutica. Nuestro motor independiente del sistema de EHR identifica candidatos para ensayos mediante coincidencia pasiva, sin compartir ningún registro de paciente ni requerir intervención manual.
Only 6% of US cancer patients participate in clinical trials. At community hospitals, that number is closer to 1-2%. (McKinsey 2024, NCI)
$0
cost to your hospital to join OpenSquare
2 Weeks
from EHR connection to first patient matches
60 Days
typical time to first revenue flowing to your institution
The Evidence Base
0%
Unaware patients
at time of diagnosis
0%
Willing to enroll
if asked
0K+
Pharma spend
per recruited patient
0%
Never participate
in any trial
"85% of patients were either unaware or unsure that participation in a clinical trial was an option at the time of diagnosis. Research found they would have been willing to enroll had they known it was possible."
Harris Interactive Survey, cited by the National Institutes of Health
Pharmaceutical companies spend between $40,000 and $80,000 to recruit a single trial participant. Your hospital already has thousands of them. With HEKMA, you earn every time one of your patients matches an active trial, without sharing a single record.
Source: Tufts Center for the Study of Drug Development, 2024
$40K–$80K
per recruited participant
that's pharma's current cost per find
Deploy enterprise-grade matching across your entire patient population in days, not months.
Integración rápida e independiente del sistema de EHR mediante la API estándar FHIR. Compatible con Epic, Cerner, Athena y otros sin desarrollo personalizado ni reemplazo de sistemas.
Cero interrupciones a los flujos de TI existentes.
La IA de Hekma analiza de forma autónoma y continua en segundo plano toda tu población de pacientes según los criterios de elegibilidad de ensayos activos.
Cero esfuerzo manual para tu personal clínico.
Tú fijas la tarifa por cada hallazgo, eliges qué indicaciones y empresas pueden acceder a tu red, y conservas la gobernanza total sobre cada término de participación.
Gobernanza total sobre los términos de participación.
Los hallazgos de coincidencia desidentificada pasiva fluyen hacia compradores farmacéuticos. Los coordinadores gestionan el contacto con los pacientes según tus condiciones. La PHI se queda contigo, los ingresos llegan a ti.
Flujos de ingresos de alto margen por cada coincidencia.
EHR Connection
1-2 days
Platform Onboarding
3-5 days
First Patient Matches
Within 2 weeks
First Revenue
30-60 days
"Patients deserve better access to clinical trials. Hospitals deserve to participate in the value created by making those connections possible."
Comprehensive technology for clinical integration at every stage of the trial lifecycle.
Transform routine clinical data into real-time trial opportunities. Our intelligent trial matching engine continuously aligns patient profiles against evolving study criteria, enabling hospitals to identify eligible participants faster, reduce screening effort, and expand access to precision-driven research programs.
Move beyond traditional recruitment models with a connected ecosystem designed to identify, engage, and guide the right patients into the right studies. Powered by clinical insights and workflow automation, hospitals can improve enrollment velocity while minimizing operational complexity for research teams.
Unify study operations, patient workflows, scheduling, compliance, and site coordination within a single intelligent platform. Built for modern research environments, our CTMS enables hospitals to manage trials with greater visibility, efficiency, and control across every stage of the study lifecycle.
Patient 360 creates a connected patient intelligence layer that brings together clinical records, research participation, care interactions, and health milestones into one unified experience. Designed for the future of personalized healthcare, it empowers providers with deeper context for more informed and continuous patient engagement.
Seamlessly connect EMR ecosystems with clinical research workflows through secure, interoperable infrastructure. By enabling structured data exchange and reducing manual effort, hospitals can unlock the full value of their clinical data to support faster study execution, operational efficiency, and scalable research innovation.
Estándares de cumplimiento e interoperabilidad
Comienza a identificar ensayos que salvan vidas para tus pacientes mientras generas nuevos ingresos para el hospital. Sin gasto de capital ni necesidad de nuevos recursos humanos.