Pew Applauds Senators Bennet and Hatch for LPAD Leadership
Pew and the Infectious Diseases Society of America applaud Senators Michael Bennet (D-CO) and Orrin Hatch (R-UT) for their leadership in supporting the creation of the Limited Population Antibacterial Drug (LPAD) pathway.
Once put in place, LPAD would expedite patient access to critically-needed antibiotics to treat serious or life-threatening infections for which there are currently inadequate treatment options.
July 31, 2013
The Honorable Michael Bennet
458 Russell Senate Office Building
Washington, DC 20510
The Honorable Orrin Hatch
104 Hart Senate Office Building
Washington, DC 20510
Dear Senators Bennet and Hatch,
We are writing today to applaud your leadership in supporting the creation of the Limited Population Antibacterial Drug (LPAD) approval pathway to expedite patient access to critically-needed antibiotics to treat serious or life-threatening infections for which there are currently few or no satisfactory treatment options. Antibiotic development has declined dramatically, while drug resistance continues to soar, leaving a very serious unmet medical and public health need.
Regulatory and economic challenges have contributed to the decline in antibiotic innovation—particularly for drugs to treat resistant infections. The LPAD pathway will encourage the development of antibiotics to treat highly resistant infections by creating a new mechanism to allow FDA to more quickly approve novel antibiotics on the basis of trials conducted on smaller subpopulations with the most serious illnesses. In contrast, antibiotics are now studied in large patient populations with a wide range of disease symptoms. A properly constructed LPAD pathway could make clinical trials shorter and less expensive and at the same time would allow for special labeling that would reflect the more limited data and help ensure limited use.
We urge you to enact legislation to create an LPAD pathway based on the principles outlined in the attached document in order to make development more feasible for the antibiotics needed most by patients. These principles also call for data collection to ensure the pathway meets its intended public health goals, including limiting the use of these new drugs to the patients for whom they are intended in order to preserve the drugs' utility and protect patients' health.
Thank you for your leadership on this critical public health issue. We look forward to working with you as you continue to develop policies to further stimulate antibiotic development. If you would like any additional information, please do not hesitate to contact our organizations at firstname.lastname@example.org or email@example.com.
Senior Director, Drugs and Medical Devices
The Pew Charitable Trusts
David Relman, MD, FIDSA
Core Principles for a limited population antibacterial drug (LPAD) pathway
As drug-resistant bacterial infections grow more common, few antibiotics are available to treat them. Today, patients need new drugs to treat increasingly common infections, particularly highly resistant serious or life-threatening ones such as those caused by carbapenem-resistant Enterobacteriaceae (CRE), a family of dangerous pathogens that pose special risk to patients in the hospital. Thomas Frieden, Director of the Centers for Disease Control and Prevention recently warned that these "nightmare bacteria" are spreading rapidly across the U.S. and are resistant to our strongest antibiotics.
Regulatory and economic challenges have contributed to the decline in antibiotic innovation for more than a decade—particularly for drugs intended to treat resistant infections in small numbers of patients. Last year, as part of the Food and Drug Administration Safety and Innovation Act, Congress enacted Generating Antibiotic Incentives Now provisions, which give additional exclusivity to qualifying new antibiotics. This law was a good first step to address some of the financial disincentives to antibiotic innovation. However, to overcome the dearth of antibiotic innovation, we need a sustained and multi-pronged strategy to spur industry and investor interest in reinvigorating the antibiotic pipeline.
As one next step, the undersigned organizations urge Congress to support creation of a new regulatory pathway for antibiotics that target special or limited patient populations — namely those suffering from serious or life-threatening infections with few or no satisfactory treatment options. The new pathway will encourage the development of antibiotics that address the greatest unmet needs (mainly caused by resistance) and get them to patients faster (preferably before the serious or life-threatening pathogen is widely spread). This pathway would speed patient access to important antibiotics by allowing them to be approved based on clinical trials with smaller numbers of patients than the trials for more widely used antibiotics. It is not feasible for antibiotics that treat serious infections due to highly resistant bacterial pathogens to be developed using traditional, large clinical trials due to the limited numbers of patients in whom these infections occur. This pathway must be designed to balance the immediate needs of patients and physicians with measures to monitor drug use in appropriate populations without placing undue burdens on Infectious Diseases physicians, nurses, hospitalists, hospital administrators, and antibiotic innovators.
The limited population antibacterial drug pathway should be created through new legislation based on the core principles outlined below. Specifically, the new law should:
Create a special designation and label (with logo) distinguishing products approved under the limited approval pathway from traditional antibiotics (e.g., drugs approved for more common infections or for infections for which satisfactory therapeutic options exist);
Acknowledge that the benefits of an antibiotic approved under the pathway outweigh the risks for the limited population for which the drugs are indicated based on smaller datasets, taking into account the seriousness of the infection and the unmet medical need. For the purposes of the legislation, the definition of unmet need should allow for the approval of multiple antibiotics per indication to ensure the antibiotic pipeline is sufficiently diverse;
Include a mechanism to collect information in order to evaluate the utility of the pathway, preferably including the FDA's Sentinel System and/or the CDC's National Healthcare Safety Network;
Require FDA to issue guidance, within one year of enactment, on acceptable clinical trial designs to demonstrate the safety and effectiveness of antibiotics approved under the pathway;
Ensure that the option to pursue this pathway for limited approval be voluntary for drug sponsors;
Allow removal of the limited population designation if FDA approves a broader indication sought by the sponsor under the traditional approval pathway;
Provide for submission and FDA review of promotional materials of products approved under this pathway, using the processes FDA has already established for accelerated approval products; and
Not attempt to regulate the practice of medicine.
American Academy of Otolaryngology — Head and Neck Surgery
American Medical Association
American Society for Microbiology
Antibiotics Working Group (Cempra, Optimer, Rib-X, Trius, Durata, The Medicines Company, Theravance)
Association for Professionals in Infection Control and Epidemiology
Infectious Diseases Society of America
Michigan Antibiotic Resistance Reduction Coalition
National Association of County and City Health Officials
National Foundation for Infectious Diseases
The Pew Charitable Trusts
Society for Healthcare Epidemiology of America
Society of Critical Care Medicine
Society of Hospital Medicine
Society of Infectious Diseases Pharmacists
Treatment Action Group
Trust for America's Health