Research, Funding and Drug Development

Improvements in outcomes for cancer patients require continued research and innovation.  ACS CAN advocates for robust federal funding for cancer research, as well as research and drug approval policies that accelerate the development of new treatments while still ensuring patient safety.

Research, Funding and Drug Development Resources:

The National Program of Cancer Registries (NPCR) at the Centers for Disease Control and Prevention (CDC) provides technical, operational, and financial support to almost all state cancer registries to help ensure data collected are representative of the U.S. population.

Clinical trials are the key step in advancing potential new cancer treatments from the research setting to the cancer care clinic, and patient participation in trials is crucial to this success.

Clinical trials are an essential step in advancing potential new cancer treatments from the research setting to the cancer care clinic, and patient participation in these trials is crucial to this success.

ACS CAN responded to the reopening of the Centers for Medicare and Medicaid Services (CMS) coverage decision for NGS testing panels.

Restrictive eligibility criteria are the second leading cause preventing patients from enrolling in cancer clinical trials.  FDA recently issued draft guidance encouraging trial sponsors to use a science-based approach that would allow a wider variety of patients to participate in cancer clinical trials.

Over 80 organizations are urging Congress to take up and pass reform to modernize the oversight of diagnostic test. 

For oncology biomarkers, commercial payers uniformly cover companion diagnostics because clinical utility is established as a component of FDA review (there is typically a therapeutic agent that is approved in parallel).

Cancer registries provide high quality cancer data to inform policy at the local, state, and national levels. That National Program of Cancer Registries (NPCR) provides technical, operational, and financial support to most state cancer registries to help ensure data collected is representative of the U.S. population.

This bill would modernize and harmonize oversight of in-vitro diagnostic tests, and ACS CAN provided feedback to draft legislative language.  The feedback addressed core issues of interest to patients.