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Platforms to Identify Candidate Drugs – PICD

Harnessing AI and Real-World Evidence to Accelerate Drug Repurposing for National Health Security Threats

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What if we could develop treatments for national health security threats faster, at lower cost, and with less risk?

Drug repurposing is one of the fastest and most cost-effective pathways for developing therapeutic medical countermeasures (MCMs). Since FDA-approved drugs and therapies already in clinical development have well characterized safety and pharmacokinetic profiles as well as established manufacturing processes, they can often be advanced for new indications with reduced time, cost and risks compared to de novo drug development.

Despite substantial advances in biomedical research, significant gaps remain in the availability of therapeutic MCMs for national health security threats.

Traditional drug development is too slow, costly and risky to meet the urgent demands of national emergencies. Developing a new therapeutic can require more than a decade, cost hundreds of millions to billions of dollars and still face a likelihood of failure in clinical development.

These challenges are compounded for emerging threats where uncertain or limited commercial markets provide little financial incentive for industry investment and as a result, create a dependency on government funding and delays in drug development during critical response windows.

Despite substantial advances in biomedical research, significant gaps remain in the availability of therapeutic MCMs for national health security threats.

Traditional drug development is too slow, costly and risky to meet the urgent demands of national emergencies. Developing a new therapeutic can require more than a decade, cost hundreds of millions to billions of dollars and still face a likelihood of failure in clinical development.

These challenges are compounded for emerging threats where uncertain or limited commercial markets provide little financial incentive for industry investment and as a result, create a dependency on government funding and delays in drug development during critical response windows.

Our Solution

Drug repurposing offers a compelling path forward by leveraging the established safety and pharmacology of existing medicines. Combined with recent advances in artificial intelligence (AI) and the growing availability of real-world data (RWD)—including electronic health records, insurance claims, and other clinical datasets—we have an unprecedented opportunity to transform how promising drug candidates are identified and prioritized.
Integrating capabilities in AI, computational biology, disease biology, RWD, and MCM development into a systematic, scalable, AI-enabled pipeline will accelerate the identification and prioritization of safe, effective repurposed therapies for emerging health threats. This will enable the timely delivery of evidence-based MCMs and strengthen national health security.

VITAL and BARDA seek to bring together complementary capabilities across the scientific and technology communities to establish platforms that can rapidly identify and evaluate promising therapeutic candidates—including repurposed drugs, repositioned drugs, natural products, and combination therapies—for emerging national health security threats.

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Key Focus Area

VITAL and BARDA seek technologies and approaches that can predict treatment benefit among patients to increase the probability of demonstrating therapeutic efficacy during clinical development and to guide treatment decisions during clinical care for improved patient outcomes.

These technologies may be based on phenotyping, sub-phenotyping, endotyping, genotyping, and/or other approaches to identify patients likely to benefit from specific treatments.

Example technologies may include but are not limited to assays, lab tests, and software as medical devices.

Addressing Heterogeneity of Treatment Effect in Health Security Threat Indications: Patient subtyping technologies to improve treatment decision-making and patient outcomes.

Online Webinar

Development, Evaluation, and Validation (DEV) Teaming

​Join us for one of our info sessions to answer all your questions about Funding Opportunities and Programs made available through the VITAL Hub. This session is perfect for innovators, entrepreneurs, and biotech startups pioneering the future of innovative therapeutics solutions. 

Goal: Systematically identify, evaluate, and prioritize existing therapeutics for new indications through an AI-enabled drug repurposing pipeline.

Goal: Systematically identify, evaluate, and prioritize existing therapeutics for new indications through an AI-enabled drug repurposing pipeline.

Potential Initial Use Cases

Potential Use Cases

Viral Hemorrhagic Fever (focus on Ebola)

Botulinum toxin (focus on intracellular intoxication)

Acute Respiratory Distress Syndrome (ARDS)

Radiation injury

Advancing Solutions That Protect Public Health

BARDA primarily develops medical countermeasures to counter acute threats and does not support research and development or acceleration in the areas of oncology or chronic disease.

However, BARDA does partner with innovators and companies developing platform and multi-use technologies. Applicants can include data from other use cases so long as BARDA funding will be used to support research and development of the BARDA-relevant use cases.

Applications Are Now Closed

Applications for Type Funding
Are Now Closed

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