OCTOBER 11, 2012 TO OCTOBER 12, 2012
CTTI Project: ABDD Unmet Need
Meeting Background:
With rising antibiotic resistance becoming an issue of global concern, the Clinical Trials Transformation Initiative (CTTI) convened a 2-day Antibacterial Drug Development Workshop on October 11-12, 2012 in Crystal City, VA. The workshop is part of a series of expert meetings to explore approaches for accelerating the development of new antibacterial drugs. The two topics of focus for this meeting were exploring a new paradigm for antibacterial drug development in areas of unmet need, and for the treatment of patients with pneumonia that develops in the hospital or while on a ventilator. This workshop followed a think tank on statistical issues that was held on August 20, 2012, in Bethesda, MD, also hosted by CTTI.
There is an urgent need to develop new antibacterial drugs to treat patients with infections caused by bacteria that are resistant to available antibiotics. Antibiotic resistance has been increasing, creating an unmet public health need. This workshop was held in collaboration with FDA’s newly formed Antibacterial Drug Development Task Force within the Center for Drug Evaluation and Research (CDER).
The purpose of the workshop was to understand the challenges in the development of new antibacterial drugs for the treatment of patients with unmet medical need (e.g., patients with multi-drug resistant bacterial infections, who have limited or no options for treatment) and to identify potential solutions that would accelerate the drug development process. Novel endpoints and possible solutions to challenges in trial design for the development of new antibacterial drugs that treat patients with hospital-acquired or ventilator-associated bacterial pneumonia (HABP and VABP) were also explored. A broad range of stakeholders participated in the meeting, including experts from academic institutions, hospitals, pharmaceutical industry, government, and patient advocacy groups.
“The workshop provided an excellent opportunity to discuss new development pathways for antibiotic drugs targeting infections for which we urgently need new antibiotic therapies. Our collaboration with CTTI on this work is part of the CDER Antibacterial Drug Development Task Force’s efforts to accelerate the development of new antibiotics to address critical patient needs”, said Edward Cox, MD, Director of the CDER’s Office of Antimicrobial Products.
Meeting Objectives:
The goal of the first day of the workshop was to define potential pathways and explore new paradigms to accelerate the development of new antibacterial drugs that would address unmet medical need, including discussing acceptable levels of uncertainty related to the risks and benefits of such treatments. The second day focused on issues in clinical trial design including endpoints and operational efficiencies specific to the development of antibacterial drugs for treating patients with hospital-acquired or ventilator-associated bacterial pneumonia (HABP/VABP).
Meeting Location:
Sheraton Crystal City Hotel, Arlington, VA
Meeting Presentations:
- 1.1 Overview of Risk-Benefit within Antibacterial Drug Development by Ed Cox
- 1.2 Antibiotic Resistance by John Bartlett
- 1.3 2012 Update of Antibiotic Resistance in the Multidrug-resistant Organism Repository & Surveillance Network (MRSN) by Emil Lesho
- 1.4Drug Development Challenges: Facilitating Collaboration by Charlene Reed
- 1.5 Clinical Trials for Rare Diseases in CDER by Kathryn O’Connell
- 1.6 Novel Approaches to Further Antibacterial Drug Development: New Approaches to the Clinical Development Program by John Rex
- 1.7 Limitations of PK-PD in Clinical Trials: Focus on Vancomycin MIC and MRSA Infection by Vance Fowler
- 1.8 Possible Clinical Trial Approaches for Areas of Unmet Need by Ed Cox
- 1.9 CTTI Think Tank for Anti-Bacterial Drug Development: Unmet Medical Need and HABP/VABP by Lisa LaVange & Daniel Rubin
- 2.1 Hospital-Acquired Bacterial Pneumonia & Ventilator-Associated Bacterial Pneumonia by Joseph Toerner
- 2.2 Direct and Indirect Measures of Treatment Effects Including Surrogate Endpoints by John Powers
- 2.3 Endpoints in HAP/VAP trials: Mortality, Clinical Endpoints, Biomarkers by Richard Wunderink
- 2.4 Identifying Non-mortality Clinical Endpoints FNIH Approach to CABP and ABSSSI by George Talbot
- 2.5 Design Strategies to Improve the Feasibility of HABP-VABP Registration Studies by P. Prokocimer
- 2.6 Issues in Operational Efficiency of HAP/VAPClinical Trials: Current and Future State by Charles Knirsch
The views and opinions expressed in this presentation are those of the individual presenter and should not be attributed to the Clinical Trials Transformation Initiative, or any organization with which the presenter is employed or affiliated.