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UNGA 2026 Political Accord Session: Precision Oncology Readiness

A high-level political session during UNGA 2026 focused on launching the New York Precision Oncology Readiness Accord. The session will frame precision oncology readiness as an access and implementation priority, bring together political, diplomatic, clinical, patient and stakeholder voices, and launch a 90-day validation process toward a 12-month implementation roadmap.

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Event details

Event type

High-Level Political Lab

Format

Afternoon high-level political accord session during UNGA week, focused on precision oncology readiness, political endorsement, stakeholder alignment and launch of a 90-day validation process.

Audience

Political and diplomatic representatives, public authorities, clinical and scientific leaders, patient advocates, oncology and diagnostics experts, regional health-system leaders, global health institutions, industry partners, funders and implementation stakeholders.

Why this event matters

Precision oncology is no longer only a scientific challenge. It is an access and readiness challenge.

Patients may become eligible for biomarker testing, clinical trial enrolment, targeted treatment or specialist care, but still face avoidable delay because systems are not ready to act. The gap is not only about innovation. It is about whether diagnostics, referral, evidence generation, reimbursement, regional capacity and patient pathways can respond when science identifies that a patient may benefit.

This UNGA-week session creates a political and public moment for a practical readiness agenda. It will present the New York Precision Oncology Readiness Accord as a shared framework for improving access, strengthening implementation and launching a 90-day validation process.

Strategic frame

The New York Precision Oncology Readiness Accord is designed as a political and operational cooperation framework. It is not a treaty and does not create legal, regulatory, reimbursement, procurement or governmental obligations unless separately agreed in writing.

The Accord is built around a simple proposition: when science identifies that a patient is eligible for better care, the system must be ready to test, refer, enrol, treat or follow that patient without avoidable delay.

The afternoon session will provide the high-level political Accord moment. A possible linked morning technical readiness lab may provide additional input on trial readiness, biomarker and diagnostic readiness, disease demonstrator pathways and regional equity. If convened, its conclusions will inform the afternoon discussion and feed into the 90-day validation process.

Core question

How can political, clinical and stakeholder cooperation make precision oncology systems ready to act when a patient becomes eligible for better care?

Agenda snapshot

13:00-13:08 | Arrival, Protocol and Opening Welcome

Opening the high-level political Accord session

IPM Alliance and host representatives will frame the afternoon as the high-level political Accord session during UNGA week, focused on turning precision oncology readiness into a shared cooperation framework for validation and follow-up.

13:08-13:18 | Readiness Framing: From Eligibility to Action

Why precision oncology readiness is now an access priority

A short strategic framing of the precision oncology readiness challenge across clinical trials, biomarkers, diagnostics, disease pathways, evidence generation and regional equity.

13:18-13:30 | Patient and Doctor Access Moment

Eligible, but not reached

A patient and clinical access moment will frame the central problem: patients may become eligible for better care, but still fail to receive timely testing, referral, trial access, treatment or follow-up.

13:30-13:42 | Opening Political Address

Precision oncology readiness as a political and access priority

Political and institutional opening remarks will position the Accord within the wider UNGA-week agenda on health systems, innovation, equity and patient access.

13:42-13:57 | Scientific and Strategic Keynote

From precision oncology innovation to readiness

Scientific and strategic keynote interventions will connect the pace of precision oncology innovation with the system conditions required for diagnostics, trial access, targeted treatment and regional implementation.

13:57-14:17 | Global Readiness and Cooperation Round

Where international cooperation can improve precision oncology access

Global institutional and public-sector voices will discuss how international cooperation can strengthen diagnostics, evidence generation, clinical trial access, regional capacity and implementation support.

14:17-14:45 | Clinical and Regional Readiness Anchors

From system barriers to practical readiness priorities

Clinical, regional and stakeholder anchors will discuss where precision oncology readiness needs to improve, including diagnostics, disease pathways, evidence generation, industry contribution, clinical adoption and regional equity.

14:45-14:55 | Presentation of the New York Precision Oncology Readiness Accord

Readiness commitments and validation process

IPM Alliance will present the Accord and its readiness commitments, setting out the shared framework for validation and follow-up after the session.

14:55-15:15 | Endorsement Statements

Political and institutional support for the Accord

Pre-cleared diplomatic and institutional signatories will endorse the New York Precision Oncology Readiness Accord and confirm support for the 90-day validation process.

15:15-15:25 | Closing: From Accord to Validation

Next steps toward the 12-month roadmap

IPM Alliance will confirm next steps, including the 90-day validation process and the basis for a 12-month implementation roadmap.

15:25-15:30 | Protocol Photo

Signature moment and reception transition

Group photo and signature moment before transition to the reception and bilateral exchange.

15:30 onward | Reception and Bilateral Exchange

Informal follow-up and stakeholder discussion

Reception and bilateral exchange to support follow-up conversations, partner engagement and validation planning.

Tracks, labs or working groups

Precision Oncology Readiness

This track frames precision oncology as an access and readiness challenge. It focuses on whether health systems can act when a patient becomes eligible for biomarker testing, clinical trial enrolment, targeted treatment, specialist referral or follow-up.

Expected output:

Shared readiness framing for the New York Precision Oncology Readiness Accord and validation process.

Diagnostics, Trials and Evidence-to-Access

This track focuses on the system conditions required to connect biomarker testing, diagnostics, clinical trial evidence, regulatory confidence, reimbursement, real-world evidence and clinical adoption.

Expected output:

Readiness priorities across diagnostics, evidence generation, reimbursement and patient pathways.

Regional Equity and Implementation Cooperation

This track examines how precision oncology access can be strengthened across countries, regions and care settings, so that access does not depend only on geography, centre capacity or local expertise.

Expected output:

Cooperation priorities for regional readiness, equity and follow-up validation.

Accord Validation and Roadmap

This track focuses on the post-session pathway: endorsement of the Accord, launch of the 90-day validation process and development of the basis for a 12-month implementation roadmap.

Expected output:

90-day validation route and foundation for a 12-month implementation roadmap.

People and contributors

Speakers

Denis Horgan

Expected outputs

This activity is designed to produce practical outputs that can support follow-up after the meeting. Depending on the format, outputs may include a public statement, implementation brief, consensus note, pathway prototype, readiness map, roadmap or stakeholder summary.

New York Precision Oncology Readiness Accord

A political and operational cooperation framework setting out shared readiness commitments for improving precision oncology access across diagnostics, trials, evidence generation, reimbursement, regional equity and patient pathways. The Accord is not a treaty

90-Day Validation Process

A structured follow-up process to validate the Accord’s readiness commitments with relevant political, clinical, patient, regional and stakeholder communities after the UNGA-week session.

12-Month Precision Oncology Readiness Roadmap

A post-validation roadmap setting out practical follow-up priorities for diagnostics, clinical trials, evidence generation, reimbursement, regional access, public-interest safeguards and patient pathways.

Readiness Commitments Summary

A concise public summary of the Accord’s six readiness commitments: no eligible patient left unidentified; no decisive test delayed without reason; no validated option kept out of reach; no geography deciding who benefits; no global trial without local access

Join us at New York Precision Oncology Readiness Accord

24 September 2026 | 20:00 - 21:00

Italian Cultural Institute, 686 Park Avenue, New York, NY 10065, United States, New York, United States • Global / North America

Interested in this event?

IPM Alliance welcomes engagement from policymakers, scientific experts, patient organisations, health-system leaders, industry partners and implementation actors.

Request Invitation